Pharmaceutical Research Jobs in Usa

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Research Associate / Senior Research Associate – Oligonucleotide Synthesis & Purification
✦ New
Salary not disclosed
San Diego, CA 7 hours ago

Location: San Diego, CA 

Seniority Level: Research Associate (RA) / Senior Research Associate (Sr. RA) 

Employment Type: Full-time 


About OliX Pharmaceuticals 

OliX Pharmaceuticals is a clinical-stage biotechnology company developing next-generation RNA interference (RNAi) therapeutics. Our proprietary asymmetric siRNA (asiRNA) platform enables precise, durable gene silencing and supports delivery platforms such as GalNAc-asiRNA for liver-targeted therapies and cp-asiRNA for local delivery (skin, eye, lung). Active clinical programs and global partnerships (including Eli Lilly, L’Oréal, and Hansoh Pharmaceutical) provide a strong foundation for discovery and development. By joining OliX, you’ll help shape the next generation of RNA medicines. 

 

Role Summary 

We are seeking a hands-on Research Associate / Senior Research Associate to support the synthesis, deprotection, purification, and analysis of chemically modified oligonucleotides that enable OliX’s RNAi pipeline. You will operate and maintain key instrumentation (e.g., HPLC/UHPLC, preparative LC, TFF, UV–Vis), document work in SOPs, batch records, and reports, and collaborate closely with RNAi chemistry, medicinal chemistry, and biology teams to advance discovery and preclinical programs. 

Key Responsibilities 

  • Execute (or Help) solid-phase oligonucleotide synthesis (SPS) and downstream processing (cleavage, deprotection, desalting). 
  • Purify and polish oligonucleotides using OPC, analytical and preparative HPLC/UHPLC, and UPLC; perform buffer exchange and concentration via TFF. 
  • Develop and optimize purification methods and in-process controls to improve yield, purity, and throughput. 
  • Perform analytical characterization (UHPLC/LC–MS, UV–Vis); compile CoAs, batch records, and data summaries. 
  • Operate, maintain, and troubleshoot lab instruments; coordinate vendor service when needed. 
  • Author and revise SOPs, work instructions, and technical reports; ensure data integrity and traceability. 
  • Work cross-functionally with medicinal chemistry and biology teams to align materials specifications and timelines. 
  • Maintain safe, compliant laboratory operations and good housekeeping (5S); participate in EHS initiatives. 
  • (Sr. RA) Mentor junior team members; lead small method-development or process-improvement projects. 

Qualifications 

Required (RA): 

  • B.S. in Chemistry, Biochemistry, Chemical Engineering, or related field with 0–3+ years of relevant lab experience (industry or academic core facility). 
  • Hands-on experience with oligonucleotide purification (e.g., OPC, HPLC/UHPLC, preparative HPLC in anion exchange and reverse phase chromatography) and basic analytical techniques (UV–Vis, KF, etc). 
  • Familiarity with solid-phase synthesis of workflows and routine instrument maintenance. 
  • Strong record-keeping and communication; proven ability to meet deadlines and work effectively in a team. 

Required (Sr. RA): 

  • B.S./M.S. in a related field with 3–6+ years of relevant industry experience in oligonucleotide synthesis/purification. 
  • Demonstrated proficiency in method development/optimization for oligo purification and in-process analytics. 
  • Experience drafting SOPs/batch records and mentoring junior staff. 

Preferred (both levels): 

  • Experience with LC–MS data acquisition/interpretation for oligonucleotides. 
  • Exposure to nucleoside/nucleotide building blocks or bioconjugation workflows supporting RNAi platforms. 
  • Familiarity with TFF operations and scale-up considerations. 

 

Why Join OliX 

  • Contribute directly to an innovative RNAi pipeline with active clinical programs and world-class partnerships. 
  • Collaborative, growth-focused environment with cross-functional exposure. 
  • Competitive compensation and benefits package (medical, dental, vision, 401(k), equity eligibility, paid holidays/year-end shutdown, stock options). 
  • Base salary range of $60,000 – $90,000 (depending on experience and qualifications) 

 

Work Environment 

  • Onsite laboratory role with routine handling of chemicals and analytical instrumentation. 
  • Some lifting (up to ~50 lb) and extended periods at the bench or operating instrumentation. 
  • Occasional off-hours support during critical runs. 

 

OliX Pharmaceuticals is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. 

 

Not Specified
Clinical Research Associate
✦ New
Salary not disclosed
Scottsdale, AZ 1 day ago

Primus Pharmaceuticals is seeking a versatile Clinical Research Associate (CRA) to support the conduct of prescription medical foods clinical trials at a growing pharmaceutical company. This role offers a mix of remote monitoring, site activities, and in-office collaboration at our Scottsdale headquarters. This role is ideal for a professional who enjoys both hands-on site engagement and strategic oversight responsibilities in a fast-paced environment.


Primus is an innovative company with novel products based on unmet needs that empowers providers and patients with prescription brands that maintain the highest level of safety without compromising efficacy. We are scaling proven brands into their next chapter, and the ideal candidate will find this motivating and have the leadership and skills to drive results.


Position Overview

The CRA will collaborate closely with Primus, the vendors, and investigative sites to ensure high-quality, compliant study execution. This role requires effective communication, and the fostering of strong site relationships and operational excellence.


Roles & Responsibilities

Vendor & Site Oversight

  • Provide operational oversight of monitoring activities, including the development of monitoring visit reports, follow-up letters, and issues escalation.
  • Track site and vendor performance against key deliverables, KPIs, and study timelines.
  • Review Trial Master File (TMF) content for accuracy and completeness.
  • Contribute to study-specific documents, including monitoring, communication, and risk management plans.


In-Field & Site Monitoring

  • Conduct qualification, initiation, interim monitoring, and close-out visits at investigational sites as needed.
  • Verify informed consent documentation, source data, case report forms (CRFs), investigational product accountability, and protocol compliance.
  • Identify and resolve protocol deviations, compliance issues, and data discrepancies directly with site personnel.
  • Serve as the primary point of contact for assigned sites, building strong relationships with investigators and staff.
  • Provide ongoing training and support to sites on protocol requirements, study tools, and GCP compliance.


Cross-Functional Support

  • Collaborate with internal teams (Clinical Development, Regulatory, Data Management, Safety, Quality) to ensure aligned trial execution.
  • Support the design, development, and refinement of essential clinical trial documents, including Case Report Forms (CRFs), monitoring plans, and study-specific instructional manuals.
  • Support audit/inspection of readiness and contribute to corrective/preventive action (CAPA) planning.
  • Assist in site and vendor governance meetings by providing operational feedback and insights.


Qualifications

Education & Experience

  • Bachelor’s degree in life sciences, nursing, pharmacy, or related field. (Requirement may be waived for candidates with 5+ years of directly relevant professional experience) .
  • 3–6 years of clinical research experience, including at least 2 years as a CRA.
  • Experience in both site/vendor oversight and direct site monitoring (pharma, biotech or CRO background preferred).

Technical Skills

  • EDC Proficiency: Strong technical experience using Electronic Data Capture (EDC) platforms for data entry, query management, and source data verification (SDV).
  • Platform Knowledge: Familiarity with industry-standard platforms such as Medidata Rave, Veeva Vault EDC, JotForm or Medrio.
  • Compliance: Deep knowledge of ICH-GCP, FDA regulations, 21 CFR Part 11, and standard clinical trial processes.

General Skills

  • Demonstrated ability to manage multiple sites/trials across various therapeutic areas.
  • Excellent communication, organizational, and problem-solving skills.
  • Willingness to travel (approximately 10–20%).
  • Comfortable working in a smaller pharmaceutical setting with the flexibility to take on broad responsibilities.


About Primus Pharmaceuticals, Inc.

Primus innovates in prescription nutritional therapies targeting metabolic causes of chronic diseases across rheumatology, dermatology, and women’s health. We develop and commercialize first-in-class products and novel deliveries in Rx drugs, medical foods, and medical devices to fill key unmet needs with universal patient access not provided by traditional pharma. Visit our website at

Not Specified
Clinical Research Coordinator
Salary not disclosed
Irvine, CA 2 days ago

M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US. M3 Wake Research continues to grow through acquisitions and uncompromising commitment to careful planning and execution in accordance with regulatory compliance.

Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US. As of today, our board-certified physicians have completed more than 7,000+ successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data.

Due to our continued growth, we are hiring for a Clinical Research Coordinator at Wake Research, an M3 company. This position is on-site and located in Irvine, CA.

Job Description

The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

Essential Duties and Responsibilities:

  • Assisting trial Investigator in screening and review of potential study participants eligibility
  • Maintaining case report forms, charts and documentation
  • Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants
  • Ensuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements
  • Collecting and entering data as necessary
  • Assist management with potential new hire selection and shadowing process
  • Assist with study start-up, maintenance, and close-out of studies as needed for those on the team
  • Ability to be flexible with study assignments

Qualifications

  • Clinical Research Coordinator with 2+ years of experience
  • Phlebotomy & EKG experience strongly preferred
  • Excellent verbal & written communication skills
  • Ability to learn quickly, read and understand complex protocols, follow very detailed directions, and multi-tasking
  • Must be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA Guidelines
  • Extensive clinical trial knowledge through education and/or experience
  • Successful completion of GCP Certification and Advanced CRC preferred
  • Detail-oriented
  • Familiarity with the Code of Federal Regulations as they pertain to human subject protection
  • Strong interpersonal skills

Additional Information

About M3:

M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, we’ve seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems.

Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements.

Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation, shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA.

Benefits:

A career opportunity with M3 Wake Research offers competitive wages, and benefits such as:

  • 401(k), 401(k) matching
  • Dental insurance
  • Disability insurance
  • Employee assistance program
  • Flexible spending account
  • Health insurance
  • Life insurance
  • Paid time off
  • Vision insurance

*This position offers a competitive pay rate of $30–$40 per hour.

*M3 reserves the right to change this job description to meet the business needs of the organization


Not Specified
Research Consultant
✦ New
Salary not disclosed
Scottsdale, AZ 1 day ago

Company Description

Darwin Research Group is a research and consulting firm focusing on healthcare delivery models. We specialize in comprehensive analyses of health systems, physician groups, and emerging payer models such as accountable care organizations and bundled payments. Our goal is to help our clients better understand the healthcare ecosystem and succeed in the ever- changing landscape. Our clients include pharmaceutical companies and medical device manufacturers.


Job Purpose

As a Research Consultant, you will be a critical member of the Research Team, assisting our clients through research and both syndicated and custom project engagements. You will also wear numerous hats at Darwin, collaborating across departments to meet client and internal requests, support sales and marketing initiatives, and manage project work. You will have the opportunity to engage with all Darwinians and make an impact in a growing organization. This dynamic role is for you if you are a team player, eager to delight clients, detail-oriented, deadline-driven, flexible, creative, and passionate about learning and adapting to change.


Job Responsibilities

  • Conduct research and contribute to product and process improvements to support our core product and service offerings.
  • Lead end-to-end research projects and custom client engagements, including research design, data collection and analysis, and the delivery of relevant and actionable recommendations.
  • Collaborate with the sales team by responding to inquiries, participating in client calls and communications, and providing support throughout the sales cycle.
  • Propose and respond to client research requests, offering strategic guidance on research methodologies, project scope, data collection and analysis, and deliverables.
  • Partner with the Research Director to create and implement operational efficiencies and product and process improvements; train the research team on workflows and best practices.
  • Support the growth of our expert research panel by managing participant recruitment, conducting interviews, and optimizing associated workflows.
  • Master our project and content management tools, including and Dropbox, to organize documentation and ensure effective cross-functional communication.
  • Proactively identify opportunities for new workflows, and product and service enhancements; work cross-functionally to implement best practices.
  • Work as a team player by working closely with our project coordinator and mentoring research colleagues and cross-functional teams.
  • Remain flexible as responsibilities evolve in response to organizational growth and changing priorities.


Knowledge, Skills, and Experience

  • Bachelor's degree (B.A. or B.S.) from a four-year college or university
  • At least 4 years of experience in syndicated or custom research in client-facing environments or similar professional environments
  • Interest and prior experience in the healthcare industry (3+ years of experience)
  • Working knowledge of MS Office Suite, Google Mail, Zoom, and related business tools
  • Proven project management experience and understanding of project lifecycles
  • Demonstrated ability to plan research, source participants, design discussion guides and research materials, and synthesize information from multiple sources – secondary research, interviews, surveys, etc.
  • Excellent communication skills with the ability to communicate in a professional and timely manner and update internal and external stakeholders on project progress
  • Organizational skills, with attention to detail and demonstrated commitment to quality
  • Highly enthusiastic, service-oriented, and responsive
  • Excellent time, resource, and project management skills
  • Self-motivated, thriving in a fast-paced, growth-oriented, deadline-driven environment
  • Quick learner with the ability to multitask with minimal supervision
  • Creative problem solver finding ways to navigate ambiguity and deliver insightful and actionable results
  • Ability to work cross-functionally


What We Offer

  • Full-time position with a competitive salary
  • Medical, dental, and vision benefits
  • 401K with guaranteed company contribution
  • Generous PTO
  • Flexible hours
  • Due to hybrid work environment, local candidates and those willing to relocate are strongly preferred


For the right person, this is an opportunity to expand your skill set and contribute to a growing company in a healthy, challenging, and collaborative environment. Many of our clients see value in our partnership and work with us year after year. Reach out to learn more!


Darwin Research Group is proud to be an equal-opportunity employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status.

This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the United States.


Website:

Not Specified
Manager of Microbiology - Opportunities for leadership in cutting-edge microbiological research (HUNT VALLEY)
Salary not disclosed
How will you make an impact?

The Manager of Quality Control (QC) - Microbiology is responsible for overseeing the Quality Control strategies and operations, including but not limited to testing function in support of the development and testing services of Phase I-III and Commercial Microbiological testing and Environmental Monitoring functions. The QC Microbiology Manager assures compliance with GMP and company specifications as well as relevant pharmacopeia compendia. The Manager identifies areas for continuous improvement and/or implementation of industry best practices and drives implementation in the laboratory. The Manger keeps Head of Quality informed of all departmental activities and product-related events.

What will you do?

- Provides technical supervision and leadership of teams that are assigned to perform environmental monitoring, product release testing, routine, and non-routine microbiological testing.

- Collaborates with other departments to provide microbiology expertise and support for smooth running of GMP manufacturing operations.

- Oversight and maintenance of quality control microbiological testing program (including sterility, bioburden, identifications and Environmental Monitoring, and outsourced test laboratories).

- Participates and carries out continuous quality improvements in the QC laboratory.

- Identifies and resolves internal quality control microbiological testing issues.

- Ensures compliance with cGMP and safety requirements within the QC microbiological laboratory.

- Schedules and provides technical oversight of microbiological testing performed internally and externally sourced supporting GMP manufacturing and pre-Clinical activities and studies.

- Participates in project specific, system, client, and vendor audits.

- Participates in internal audits of GMP QC data and records, monitoring files and study files. Reviews new and executed documents for compliance to stated Pii SOPs, formats, and regulatory requirements (especially protocols, deviations, investigations, amendments, etc.)

- Writes and/or reviews SOPs pertaining to Quality Control microbiological operations, STM’s (standard test methods), and qualification and stability protocols (if needed) to insure appropriate codification of GMP procedures.

- Ensures QC microbiological laboratories and facilities are always in an audit ready status.

- Serves as a back up to QC client rep in meetings for microbiological matters.

- Acts as technical QC microbiological SME in support of client needs and projects and during third party inspections/audits.

- Interacts and communicates with customers to assure expectations are established, agreed to, and achieved.

- Engage actively with Project Management and other department functions to ensure the GMP programs are properly supported to achieve expectations; maintain effective and professional communication between all parties, including the customer.

- Identify, maintain, and report functional KPIs to site management.

- Perform other duties as assigned.

How will you get here?

Education:

- Bachelor’s degree, or equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities.

Experience:

- Preferred 15+ years relevant work experience in Quality Control laboratories

- Preferred three to five (10-15) years of leadership/ supervisory/management experience in commercial laboratory operations.

- 10 years of applied Microbiology experience in a commercial pharmaceutical, GMP manufacturing environment (preferably parenteral and in a CMO/CDMO/Clinical Environment)

- Experience in Analytical or Microbiological testing including Environmental Monitoring required

- Auditing and compliance experience in a biopharmaceutical or clinical research organization and/or federal regulatory experience is strongly preferred.

- Experience in a GMP environment to include ICH guidelines, FDA guidelines, USP and EP, and other applicable regulatory guidance’s (US and EU).

Knowledge, Skills, Abilities:

- Must possess excellent communication and writing skills, patience, professionalism, and ability to effectively interact with staff and management alike (transversely collaborative) across functional groups and levels.

- Demonstrate the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates.

- Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision.

- Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as required.

- Must be able to comprehend and follow all applicable SOPs.

- Demonstrate knowledge and experience with electronic Quality Management Systems such as MasterControl and Trackwise.

- Demonstrate solid understanding on the current federal, local, and international regulations regarding the production, testing, and release of drug substances and products.

- Good understanding of cGMPs, industry, and regulatory standards and guidelines.

- Demonstrate familiarity with Microsoft programs like Word, Excel, PowerPoint, Project, Teams, Outlook, etc.

- Demonstrate the ability to portray the appropriate level of integrity and professionalism.

- Demonstrate the ability to communicate effectively with management, staff, regulators, and client representatives in written and verbal formats.

- Demonstrate the ability to complete tasks accurately and according to established and shifting timelines.

- Demonstrate the ability to make quality scheduling, resource allocation, and priorities decisions.

- Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment.

- Results-oriented and efficient.

- Creative and open-minded who fosters an environment in which sharing of ideas is encouraged.

- Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally).

- Demonstrate the ability to work well in a cross-functional team environment.

- Must communicate fluently in English and have legible handwriting.

Physical Demands:

- Ability to travel between and within facilities to visit staff, operations, and projects, as needed.

- Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary).

- Ability to lift up to 40 pounds on occasion.

- Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).

What can Jabil offer you?

Along with growth, stability, and the opportunity to be challenged, Jabil offers a competitive benefits package that includes:

- Medical, Dental, Prescription Drug, and Vision Insurance with HRA and HSA options
- 401K Match
- Employee Stock Purchase Plan
- Paid Time Off
- Tuition Reimbursement
- Life, AD&D, and Disability Insurance
- Commuter Benefits
- Employee Assistance Program
- Pet Insurance
- Adoption Assistance
- Annual Merit Increases
- Community Volunteer Opportunities

Apply Today!
temporary
Professor - Biomedical Engineering, Georgia Research Alliance (GRA) EminentScholar
✦ New
Salary not disclosed
Atlanta, GA 1 day ago
Apply for JobJob ID292426

LocationAtlanta, Georgia

Full/Part TimeFull-Time

Regular/TemporaryRegular

Add to Favorite JobsEmail this Job

About Us

Overview

Georgia Tech prides itself on its technological resources, collaborations, high-quality student body, and its commitment to building an outstanding and diverse community of learning, discovery, and creation. We strongly encourage applicants whose values align with our institutional values, as outlined in our Strategic Plan. These values include academic excellence, diversity of thought and experience, inquiry and innovation, collaboration and community, and ethical behavior and stewardship. Georgia Tech has policies to promote a healthy work-life balance and is aware that attracting faculty may require meeting the needs of two careers.

About Georgia Tech

Georgia Tech is a top-ranked public research university situated in the heart of Atlanta, a diverse and vibrant city with numerous economic and cultural strengths. The Institute serves more than 45,000 students through top-ranked undergraduate, graduate, and executive programs in engineering, computing, science, business, design, and liberal arts. Georgia Tech's faculty attracted more than $1.4 billion in research awards this past year in fields ranging from biomedical technology to artificial intelligence, energy, sustainability, semiconductors, neuroscience, and national security. Georgia Tech ranks among the nation's top 20 universities for research and development spending and No. 1 among institutions without a medical school.

Georgia Tech's Mission and Values

Georgia Tech's mission is to develop leaders who advance technology and improve the human condition. The Institute has nine key values that are foundational to everything we do:

Students are our top priority.
We strive for excellence.
We thrive on diversity.
We celebrate collaboration.
We champion innovation.
We safeguard freedom of inquiry and expression.
We nurture the wellbeing of our community.
We act ethically.
We are responsible stewards.

Over the next decade, Georgia Tech will become an example of inclusive innovation, a leading technological research university of unmatched scale, relentlessly committed to serving the public good; breaking new ground in addressing the biggest local, national, and global challenges and opportunities of our time; making technology broadly accessible; and developing exceptional, principled leaders from all backgrounds ready to produce novel ideas and create solutions with real human impact.

About the Wallace H. Coulter Department of Biomedical Engineering at the Georgia Institute of Technology and Emory University

The Wallace H. Coulter Department of Biomedical Engineering at Georgia Tech and Emory University has a student body of 1,200 undergraduates, 425 graduate students, and 80 primary and 73 program faculty. In 2025 US News Graduate Program Rankings placed the department as the #2 ranked department in BME in the United States and our Undergraduate Program as the #2 department in the United States. Since its beginning, the unique partnership between two of the nation's leading public and private entities has been an innovation engine for research and education. Combining the engineering and medical strengths at Georgia Tech and Emory, we are focused on solving some of the toughest problems facing our state, the nation, and the world.



Location

Atlanta, GA



Job Summary

The Wallace H. Coulter Department of Biomedical Engineering at the Georgia Institute of Technology & Emory University invites applications from exceptional senior candidates working in the area of Neuroengineering, broadly defined. The successful candidate will be named the Georgia Research Alliance (GRA) Eminent Scholar in Neuroengineering, an endowed position specific to the Georgia Tech campus. GRA eminent scholars are expected to engage in or contribute to translational and/or economic development efforts in their field. Applicants should have earned a Ph.D. or equivalent degree. Appointment is expected at the rank of full professor with tenure.

The department seeks a visionary scholar-educator and proven leader in high impact and emerging areas of importance to human health and biomedicine. We are specifically interested in the areas of neuroengineering and neuroscience, particularly developing and using approaches in machine learning and AI, with neurotranslational potential. Along with excellent scholarship, candidates are expected to have demonstrated strong leadership in building and leading extramurally funded research programs, noteworthy dedication to innovative teaching and mentoring of diverse undergraduate and graduate student bodies, as well as national and international recognition. Of particular interest are candidates with an established and active record of accomplishment in leading large multi-institution and multi-disciplinary collaborative research efforts and a vision for developing the next generation of neuroengineering tools to facilitate emerging areas such as interactive neurotechnologies, brain computer interfaces, neuroAI, neural control of sensing and moving, the neural bases of decision making and cognitive function, and the neuroscience of neurological or psychiatric disorders.

Georgia Tech prides itself on its technological resources, collaborations, high-quality student body, and its commitment to building an outstanding and diverse community of learning, discovery, and creation. We strongly encourage applicants whose values align with our institutional values, as outlined in our Strategic Plan. These values include academic excellence, diversity of thought and experience, inquiry and innovation, collaboration and community, and ethical behavior and stewardship. Georgia Tech has policies to promote a healthy work-life balance and is aware that attracting faculty may require meeting the needs of two careers



Responsibilities

The successful candidate will interact with a vibrant and rapidly growing multi-disciplinary community across Georgia Tech, Emory, and greater Atlanta. Examples include: the Georgia Tech/Emory Neural Engineering Center; the newly-formed GT Institute for Neuroscience, Neurotechnology, and Society (INNS), crosscutting multiple Colleges; the McCamish Parkinson's Disease Innovation Program; researchers and educators spanning various basic science and engineering departments across Emory and Georgia Tech, as well as clinical departments such as the Emory Department of Rehabilitation, Division of Physical Therapy, Neurology, Neurosurgery, and the Emory Brain Health Center.



Required Qualifications

A PhD in engineering or related field is required by the start of the appointment.



Preferred Qualifications

  • A PhD in engineering or related field is required by the start of the appointment.
  • The ability to teach and mentor a student body
  • The ability to promote a welcoming educational/work environment
  • The ability to mentor and assist students interested in pursuing graduate education
  • The ability to engage students in experiential learning activities and pedagogy that support student success
  • The ability to engage in high-impact practices that support deep learning for student success





Required Documents to Attach

Applicants should submit 1) a letter of application, 2) curriculum vitae, 3) a statement of research interests, 4) a description of teaching interests, 5) A statement that in two pages or less outlines how the applicant's professional and academic experiences have prepared them to support and apply Georgia Tech's mission and values , and 6) the names and contact information for at least three references. Application materials should be submitted as .PDF files



Apply Before Date

Applications will be considered beginning January 15, 2026, but the search will continue until the positions are filled.



Contact Information

Requests for information may be directed to .



USG Core Values

The University System of Georgia is comprised of our 26 institutions of higher education and learning as well as the System Office. Our USG Statement of Core Values are Integrity, Excellence, Accountability, and Respect. These values serve as the foundation for all that we do as an organization, and each USG community member is responsible for demonstrating and upholding these standards. More details on the USG Statement of Core Values and Code of Conduct are available in USG Board Policy 8.2.18.1.2 and can be found on-line at policymanual/section8/C224/#p8.2.18_personnel_conduct.

Additionally, USG supports Freedom of Expression as stated in Board Policy 6.5 Freedom of Expression and Academic Freedom found on-line at policymanual/section6/C2653.



Equal Employment Opportunity

The Georgia Institute of Technology (Georgia Tech) is an Equal Employment Opportunity Employer. The Institute is committed to maintaining a fair and respectful environment for all. To that end, and in accordance with federal and state law, Board of Regents policy, and Institute policy, Georgia Tech provides equal opportunity to all faculty, staff, students, and all other members of the Georgia Tech community, including applicants for admission and/or employment, contractors, volunteers, and participants in institutional programs, activities, or services. Georgia Tech complies with all applicable laws and regulations governing equal opportunity in the workplace and in educational activities.

Equal opportunity and decisions based on merit are fundamental values of the University System of Georgia ("USG") and Georgia Tech. Georgia Tech prohibits discrimination, including discriminatory harassment, on the basis of an individual's race, ethnicity, ancestry, color, religion, sex (including pregnancy), national origin, age, disability, genetics, or veteran status in its programs, activities, employment, and admissions. Further, Georgia Tech prohibits citizenship status, immigration status, and national origin discrimination in hiring, firing, and recruitment, except where such restrictions are required in order to comply with law, regulation, executive order, or Attorney General directive, or where they are required by Federal, State, or local government contract.



Other Information

This is not a supervisory position.
This position does not have any financial responsibilities.
This position will not be required to drive.
This role is not considered a position of trust.
This position does not require a purchasing card (P-Card).
This position will not travel
This position does not require security clearance.



Background Check

Successful candidate must be able to pass a background check. Please visit employment/pre-employment-screening



Not Specified
Pharmaceutical Field Sales Representative
✦ New
Salary not disclosed
Houston, TX 7 hours ago

Specialty Account Manager/ Pharmaceutical Field Sales Representative


Location: Houston


Who We Are


Aucta Pharmaceuticals is an emerging product development pharmaceutical company. Aucta is implementing a branded/generic hybrid model, generating both near-term product revenue and mid/long-term investment return. We aim to become a significant specialty pharmaceutical company in the U.S. marketplace integrating R&D, manufacturing, and commercialization. We focus on improved dosage forms for patients with a therapeutic focus in CNS, Ophthalmology, and Inhalation areas.


Aucta successfully launched its first branded product, Motpoly XR, in the epilepsy space with a targeted sales force in mid-February 2024. We are now expanding our commercial presence in the neurology/epilepsy sector by increasing our field sales territories to 20. Our objective is to enhance our marketing, managed care, and sales capabilities to support future pipeline products in neurology over the coming years



Position Description

The Specialty Account Manager will be an integral part of a sales team developing and managing an assigned territory. The primary responsibility of the Sales Representative will be to develop and manage a designated regional territory with the goal of maximizing and reaching sales forecasts. Expectations for the Sales Representative include being a self-starter, a team player, and responsible for identifying, ranking, prospecting, and developing key neurology practices. This also includes hospital-based business relationships within the targeted regional territory. You will be overseeing and leading the identification of business opportunities, building and fostering customer relationships, and ensuring the effective presentation of Motpoly XR to meet/exceed sales forecasts and goals.


We kindly request that applications be submitted only by individuals currently residing within the designated territory.




Who You Are

Energetic Pharmaceutical Sales person with a competitive spirit and experience in new drug product launches, preferably in the Epilepsy/Neurology space. You are an award-winning salesperson with a history of sales success within the pharmaceutical, biotechnology, or medical industry. At a minimum, you bring three years of pharmaceutical sales experience along with a Bachelor’s degree.


Key responsibilities for this role include:


  • Effectively communicate appropriate, therapeutic, disease state, and product information to customers to successfully promote the use of Motpoly XR within the territory
  • Utilize effective selling techniques and marketing strategies to create and expand Motpoly XR’s demand.
  • Develop a business plan for the assigned territory that is consistent with Aucta’s sales plans, strategies, and objectives.
  • Conducts quality sales conversations with all targeted customers.
  • Achieve quarterly sales goals within the territory while adhering to all ethical sales practices and required regulations.
  • Understands and demonstrates targeting principles.
  • Develop pre-call planning strategy for key targets.
  • Develop positive and interactive relationships with peers, customers, and Company support team members.
  • Responsible for ensuring high levels of call and field productivity.
  • Gathers and utilizes information from offices, pharmacists, and others to develop and implement specific strategies for territory prescribers.
  • Leverages sample program, literature, and other items to ensure physician awareness of Aucta Products.
  • Differentiates products from all competitors and responds to customer issues confidentially and appropriately.
  • Actively pursue continuous learning and professional development on efficient sales, communication & product knowledge training.


Minimum Qualifications for this role are as follows:


  • Bachelor’s degree required.
  • A minimum of 2 years of biotech/pharma sales and product promotion is required preferably in the CNS therapeutic area.
  • Proven track record of consistent sales success and experience developing, implementing, executing, and monitoring success within each account.
  • Successful launch experience preferred, preferably in the CNS therapeutic area.
  • Proven business acumen with a strong track record of consistently exceeding territory performance goals.
  • Demonstrated success in influence and negotiation skills.
  • Excellent oral, written, interpersonal, and listening skills.
  • Demonstrated leadership skills, including the ability to take initiative and drive results independently. Demonstrates proficiency in key competencies essential for success in this role.
  • Demonstrated ability to work independently and as a highly motivated self-starter within a team environment to deliver results. Ability to learn, apply, and effectively communicate products and disease states.
  • Proficiency in Excel, Word, MS Teams, and Outlook. Flexibility to travel up to 30 percent, with potential variation based on territory size. Overnight stays may be required.
  • Must live within the territory/geography of responsibility
  • Possession of a valid Driver’s License with a clean driving record.


Benefits

We offer a competitive benefits package to all employees, including:

  • Health Benefits (Medical, Dental, Vision)
  • 401k
  • Life Insurance
  • Disability
  • PTO


Aucta Pharmaceuticals is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.


Please refrain from forwarding unsolicited resumes from agencies to Aucta Pharmaceuticals. Aucta is not liable for any fees incurred from the use of resumes from this source. We only compensate agencies with whom we have a formal agreement. For recruitment inquiries, please reach out directly to our Human Resources department.

Applications will be accepted until the position is filled.


#LI-AG1

Not Specified
Posting Job Pharmaceuticals Sales Representative, Diabetes - Atlanta West
✦ New
Salary not disclosed
Atlanta, GA 1 day ago
Pharmaceutical Sales Representative Diabetes/Endocrinology

The Pharmaceutical Sales Representative Diabetes/Endocrinology is responsible for the achievement of commercial objectives in the assigned territory in alignment with Xeris' corporate goals. Reporting to the Regional Business Director (RBD), the PSR will participate in the development and execution of strategic and tactical territory and account level business plans in order to meet and exceed sales goals and business objectives.

Responsibilities
  • Deliver on corporate objectives specific to territory.
  • With RBD and internal business partner input, develop, evolve, and execute territory and account level business plans.
  • Engage RBD with timely recommendations to eliminate or minimize barriers to progress specific to marketplace trends, business opportunities and threats, competitive information, etc.
  • Leverage internal expertise to maximize field impact.
  • Work with Regional Business Directors, Channel/Trade & Market Access Teams, and Sales Representatives to develop territory-specific strategies to ensure patient access to Xeris products.
  • Manage territory budget and resource allocations to maximize return on investment.
  • Create a face to the internal and external customer that demonstrates Xeris' commitment to bringing value and solutions to the customers and patients we serve.
  • Collaborate with peers, marketing, and training personnel to share information and implement territory initiatives/strategies.
  • Create, build, and maintain relationships and regular communications and sales efforts with physicians & other health care providers, and all others pertinent to Xeris' business.
  • Professionally and ethically represent Xeris to external customers (including but not limited to hospitals, IDNs, individual physicians and health care providers, and local diabetes chapters) and foster their respect by demonstrating our commitment to advancing patient care and outcomes.
  • Professionally and ethically represent Xeris internally and foster professionalism within, among, and beyond the region.
  • Take responsibility for ongoing professional development to maximize effectiveness in advancing Xeris' objectives.
  • Leverage internal training and development.
  • Refine ability to navigate complex and multi-layered accounts
  • Refine ability to effectively communicate and engage with customers while leveraging Xeris internal resources.
Qualifications
  • Bachelor's Degree in Health Sciences, Business/Marketing, or related field.
  • Sales position level is determined by candidate experience and capabilities. At Xeris Pharmaceuticals, levels of consideration are based on the following:
    • 2+ years of experience in field commercial positions, including but not limited to: sales representative, hospital representative, sales trainer, and marketing
    • 5+ years of experience in bioscience commercial positions, including but not limited to: sales representative, hospital representative, sales training, marketing and regional account manager
  • Recent experience in bioscience and/or diabetes is highly desirable
  • Able to create and execute a thoughtful business plan adjusting when needed in order to meet organizational goals.
  • Proficient in understanding key data and metrics and utilizing this information to improve business performance.
  • Thrives in ambiguity and uncertainty; can adapt quickly in any situation and asks questions to increase depth of understanding.
  • Competencies: Self-directed, Organizational skills, Verbal and Written Communication skills, Time Management, Presentation skills, Project Management skills, Problem Solving, Negotiation skills, Influencer, Adaptability
  • Working Conditions: Position may require periodic evening and weekend work, as necessary to fulfill obligations. Travel requirements will vary by territory but will minimally be 20%.

As an equal employment opportunity and affirmative action employer, Xeris Pharmaceuticals, Inc. does not discriminate on the basis of race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, veteran status, genetics or any other characteristic protected by law. It is our intention that all qualified applications are given equal opportunity and that selection decisions be based on job-related factors.

The anticipated base salary range for this position is $85,000 to $130,000. Final determination of base salary offered will depend on several factors relevant to the position, including but not limited to candidate skills, experience, education, market location, and business need. This role will include eligibility for commission and equity. The total compensation package will also include additional elements such as multiple paid time off benefits, various health insurance options, retirement benefits and more. Details about these and other offerings will be provided at the time a conditional offer of employment is made. Candidates are always welcome to inquire about our compensation and benefits package during the interview process.

NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization.

Not Specified
Assistant/Associate Professor of Research and Medical Investigator
✦ New
Salary not disclosed
Baton Rouge, LA 1 day ago
At the forefront of medical discovery as it relates to understanding the causes of obesity, diabetes, cardiovascular disease, cancer and dementia, Pennington Biomedical Research Center is a campus of Louisiana State University and conducts basic, clinical and population research. The Center includes Basic Science, Clinical Research, and Population and Public Health, enabling both focused research and translational science. Research at Pennington Biomedical is supported broadly by multiple NIH Research Centers , and includes approximately 65 faculty and 20 postdoctoral fellows who comprise a network of 44 laboratories and 13 highly specialized core service facilities. Pennington Biomedical is located within state-of-the-art research facilities on a 222-acre campus in Baton Rouge, Louisiana.
Faculty
LSUPBRC ExD - Clinical Science (Juan Lertora (
LSU - Pennington Biomedical
Pennington Biomedical Research Center , a world-renowned academic research institute of Louisiana State University, is seeking an Assistant or Associate Professor of Research and Medical Investigator in Clinical Science.
This faculty position will be split 70% for clinical work and 30% for independent research program, and will oversee clinical trials, perform safety medical reviews, participate in the development of clinical trials, and oversee the medical aspects of clinical research projects initiated by scientists at Pennington Biomedical.
Research
Establish, develop, and sustain an independent, externally funded research program in endocrinology and metabolism, with a strong expectation of securing major peer-reviewed support (e.g., Design and conduct innovative, rigorous, and impactful research that advances the scientific understanding of metabolic health and disease.
Disseminate research findings through publication in high-impact, peer-reviewed journals and presentation at regional, national, and international scientific meetings.
Actively engage in interdisciplinary collaboration with principal investigators and research teams across Pennington Biomedical to foster synergistic science and enhance translational impact.
Contribute to the academic mission through mentorship and supervision of trainees, including graduate students, postdoctoral fellows, and research staff, as appropriate.
Participate in scholarly and professional service activities, including peer review of manuscripts and grants, service on study sections or advisory panels, and active involvement in relevant professional societies.
Support institutional initiatives by contributing to program development, collaborative grant submissions, and strategic research priorities.
Maintain compliance with all regulatory, ethical, and institutional requirements related to research conduct.
Demonstrate a commitment to excellence in research, collegiality, and service consistent with the standards of an Assistant/Associate Professor appointment.
Provide clinical coverage within the Clinical Research Unit to support active research protocols, ensuring high-quality, compliance, and participant-centered care.
Serve as Medical Investigator or Co-Investigator on funded clinical and translational research projects, contributing to study design, implementation, safety oversight, and interpretation of clinical outcomes.
Participate in an equitable on-call rotation with medical staff to support Clinical Research Unit operations and ensure continuity of care for research participants.
Contribute clinical expertise to interdisciplinary research teams, supporting the integration of clinical insight into ongoing and future endocrinology and metabolism studies.
Engage in clinical activities that advance the institution’s translational mission, which may include service in Pennington Biomedical treatment clinics as determined by programmatic needs, medical staff coverage, and the Executive Director.
Adhere to all institutional, regulatory, and ethical standards related to clinical care and human subjects research.
MD or DO degree from an accredited medical school.
Eligibility for medical licensure in the State of Louisiana, with appointment contingent upon successful licensure and credentialing/privileging at all applicable practice sites.
Completion of residency in Internal Medicine or Family Practice, with a minimum of 3–5 years of post-residency clinical and/or academic experience.
Ability to work effectively in a collaborative, multidisciplinary academic and clinical environment.
Strong organizational and time-management skills with ability to balance clinical, research, and scholarly responsibilities.
Commitment to collaborative, interdisciplinary team science.
Fellowship training in Endocrinology, Metabolism, or a related specialty (or equivalent research experience).
Experience in a research setting – implementation of Clinical Trials for investigational drugs and/or biologics.
Demonstrated track record of peer-reviewed publications in relevant fields.
Experience serving as Principal Investigator or Co-Investigator on clinical or translational research studies.
Demonstrated experience in clinical and/or translational research, including participation in funded studies.
Record of peer-reviewed scholarly publications.
Pennington Biomedical Research Center (PBRC) is an equal employment opportunity employer and serves as a model employer for individuals with disabilities.
Not Specified
Research Manager (Healthcare)
✦ New
Salary not disclosed
Scottsdale, AZ 1 day ago

Darwin Research Group is seeking an operations-minded, people-focused Research Manager to lead our research team and ensure efficient, high-quality production of our flagship product: a library of syndicated profiles analyzing the most important hospital systems, cancer treatment centers, and physician groups in the United States, as well as other company research offerings.

In this role, you will report to the Research Director. You will be the operational anchor, working with substantial independence to manage people, optimize workflows, maintain standards, and continuously improve how Darwin’s products are produced.

This is a hands-on leadership role for someone who thrives at the intersection of people management, production excellence, and content quality. You do not need to arrive as a health care expert. Yet, you must bring the intellectual curiosity, motivation, and learning aptitude required to thrive in a start-up environment, establish product knowledge and credibility quickly, and build deeper expertise over time.The position is located in our Scottsdale office.


Key Responsibilities

Team Leadership & Supervision

  • Mentor and manage a team of 10-12 early-career researchers responsible for producing the company’s primary product and other research offerings
  • Handle day-to-day personnel tasks, conduct performance reviews, deliver coaching sessions, and lead career development planning for the team
  • Identify, develop, and promote growth of high-potential team members toward advanced research analyst and consultant roles
  • Lead hiring, onboarding, and training of new research team members
  • Foster a culture of accountability, integrity, quality, and continuous development


Production & Operations Management

  • Own the end-to-end workflow and deadlines for research product production
  • Balance workloads across the team, optimizing for capacity, skill development, and deadlines
  • Work closely with the Operations team, the owner of our internal systems, research applications, and client delivery processes, to ensure production and workflow changes are properly reflected in systems
  • Track throughput and quality, identify and resolve bottlenecks, and make resource allocation/staffing recommendations to the Director
  • Drive the general research interview process that provides valuable insights for the syndicated profiles and other Darwin product offerings


Content Quality & Subject Mastery

  • Develop deep knowledge of our profile and research report content, research methodologies, and quality standards
  • Review work for completeness, consistency, and proper response to editorial feedback
  • Ensure interview insights are accurately incorporated into each report; maintain high standards for interview analysis, annotation, and incorporation into research reports
  • Maintain awareness of relevant healthcare industry trends to build credibility as a leader who can provide meaningful content, analytical feedback, and report offering recommendations
  • Collaborate with editorial staff and peer reviewers on language, style, and layout decisions


Strategic Support & Product Input

  • Over time, grow to support the Director’s strategy, client, and commercialization efforts
  • Bring a “product manager” mindset to Darwin report offerings: what do our clients need, what’s working, what’s not, what needs to change?
  • Identify holes, gaps, or opportunities to improve product offerings
  • Support custom research projects and client engagements when appropriate (especially after year one)


What Success Looks Like

  • Product production is smooth and consistent, with met deadlines and top-quality output
  • Assigned researchers understand expectations, grow in capability over time, and see a career development path
  • Career paths and workflows are clear, efficient, and proactively managed
  • The Research Director spends more time on strategic work, not supervising daily production operations
  • You quickly become a credible voice in discussions about improving research and product content and offerings, quality, and structure


Qualifications


Required

  • 5–8 years of professional experience, including at least 2 years in a formal team leadership, operations, or project management role
  • Proven track record in managing workflows, prioritizing competing demands, and optimizing team productivity in a fast-paced environment
  • Demonstrated ability to mentor early-career professionals, deliver constructive performance feedback, and design clear career progression paths
  • Strong organizational skills, exceptional attention to detail, and the ability to make sound, independent decisions
  • Ability to rapidly understand new industries, concepts, and research methodologies
  • Excellent written and verbal communication skills with the high emotional intelligence needed to navigate a growing startup environment
  • Experience in healthcare and/or life sciences (deep expertise not required)
  • Comfort with ambiguity, shifting priorities, and evolving product requirements


Strongly Preferred

  • Direct experience in research operations, publishing, or content creation
  • Experience with standardized content products, syndicated reports, or recurring publication cycles
  • Experience working in a start-up environment
  • Track record of significant, large-scale process improvement
  • Bachelor’s degree in business, communications, social sciences, or related field


Who Thrives in This Role

You're energized by making things run smoothly. You like building systems, solving workflow puzzles, and creating order out of chaos. You're equally comfortable having a coaching conversation with a struggling team member or building a capacity planning spreadsheet. You can credibly assess the quality of work even in areas where you're not the official expert. You prefer to solve problems yourself rather than escalate everything up the chain- but you know when to involve your boss. You enjoy coaching and managing a team and working in an evolving environment.

Not Specified
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