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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
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
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
Physician Assistant - Clinical Research (Sub-Investigator)
Salary not disclosed
Brooklyn, NY 6 days ago

Physician Assistant – Clinical Research (Sub-Investigator)

Location: Brooklyn, NY


About Brooklyn Clinical Research:

Brooklyn Clinical Research was founded to increase access to clinical trials for underrepresented populations. Clinical-trial enrollment should accurately represent the broader population. In meeting this objective, we help improve therapeutic efficacy and safety for all individuals.


Position Overview:

We are seeking a clinically adept, highly motivated Physician Assistant to join our growing research team as a Sub-Investigator. This is a hands-on clinical research role, working alongside our full-time Principal Investigator (MD) to conduct industry-sponsored clinical trials.


The ideal candidate will thrive in a fast-paced, dynamic environment where flexibility, strong clinical decision-making, and attention to detail are essential. You will receive full training in clinical research and GCP, and you will play a key role in the daily conduct of clinical trials — performing protocol-specific assessments, managing study visits, and ensuring participant safety and regulatory compliance.


Key Responsibilities:

  • Serve as a Sub-Investigator on assigned clinical trials under supervision of the Principal Investigator.
  • Perform protocol-required medical evaluations, including detailed histories, physical exams, safety assessments, and medical oversight of study participants.
  • Administer investigational products (e.g., vaccines, injectables) according to protocol.
  • Perform and oversee clinical procedures including phlebotomy, vital signs, ECGs, and other protocol-specified tests.
  • Assess and document adverse events and serious adverse events according to FDA and Sponsor guidelines.
  • Maintain thorough, timely, and accurate source documentation and electronic data entry (EDC, eSource, CTMS).
  • Collaborate closely with clinical coordinators, regulatory staff, sponsors, and CROs.
  • Participate in monitoring visits, audits, and inspections.
  • Maintain comprehensive knowledge of study protocols, informed consent documents, and regulatory requirements.
  • Participate actively in team meetings, contributing to ongoing process improvement as our site grows.
  • Act as a supplementary Clinical Research Coordinator on an as-needed basis.


Qualifications:

  • Graduate of an accredited Physician Assistant program (required).
  • Active Physician Assistant license in New York State (required).
  • Prior clinical research experience is a strong plus but not required.
  • Extensive background in direct patient care.
  • Current BLS/CPR certification.


Key Attributes for Success:

  • Excited to work in a fast-paced clinical environment where protocols and patient needs can vary daily.
  • Strong clinical acumen and independent judgment.
  • Detail-oriented with excellent documentation skills.
  • Highly organized with the ability to manage multiple protocols simultaneously.
  • Excellent communication and teamwork skills.
  • Commitment to patient safety, protocol adherence, and research integrity.
  • Spanish fluency or medical Spanish is a plus but not required.


Position Details:

  • Full-time, salaried position, Monday–Friday. Occasional weekend work may be required during high-volume vaccine periods.
  • Anticipated Start Date: ASAP
  • Salary Range: $140,000 to $170,000 depending on experience.


Why Join Us:

This is an excellent opportunity for a PA who is interested in advancing their career into clinical research while maintaining direct patient interaction. You will be a key member of a high-performing, mission-driven team with meaningful opportunities for professional growth as our research site expands.


Notice to Recruiters and Agencies

We do not accept unsolicited resumes from headhunters, recruitment agencies, or fee-based recruitment services. Please do not forward resumes to our employees or any company location/contact. Brooklyn Clinical Research is not responsible for any fees related to unsolicited resumes. We will consider any CV or resume received without a prior, signed agreement to be the property of Brooklyn Clinical Research, and we will process it accordingly without fee or obligation.

Not Specified
Research Engineer - Applied Machine Learning
✦ New
Salary not disclosed
Ashburn, VA 1 day ago

Research Engineer – Applied Machine Learning

Novateur stands for Innovation. We value creativity, vision, collaboration, and above all, ambition to innovate. Novateur Research Solutions is an R&D firm located in Northern Virginia, developing intelligent systems that push the boundaries of computer vision, AI, and large-scale learning.

We are seeking Research Engineers to advance the state of the art in large-scale machine learning, spatiotemporal modeling, and multimodal reasoning. Our projects span object tracking, re-identification, geo-localization, chemical and biological defense, and scene understanding. You will work at the intersection of software engineering and applied research, turning novel algorithms into robust, deployable systems.


Responsibilities:

• Prototype and optimize algorithms in computer vision and machine learning.

• Build scalable training and inference pipelines on cloud platforms (AWS EKS).

• Perform data curation, model evaluation, and system integration.

• Collaborate with academic and government research partners.


Requirements:

• BS or MS in Computer Science, Engineering, Applied Math, or related field.

• Experience with PyTorch or TensorFlow and scalable model training.

• Strong background in algorithms and software design.

• Excellent communication and technical writing skills.

• U.S. Citizen or Permanent Resident.


Preferred:

• Experience with geospatial data (PostGIS, GeoJSON, QGIS).

• Familiarity with Kubernetes and distributed data systems.


Why Novateur?

Join a team that values creativity and initiative. Our engineers have freedom to innovate, collaborate with top researchers, publish research in major scientific conferences, and see their ideas deployed in impactful applications.


Company Benefits:

Novateur offers competitive pay and benefits comparable to Fortune 500 companies that include a wide choice of healthcare options with generous company subsidy, 401(k) with generous employer match, paid holidays and paid time off increasing with tenure, and company paid short-term disability, long-term disability, and life insurance.

We offer a work environment which fosters individual thinking along with collaboration opportunities within and beyond Novateur. In return, we expect a high level of performance and passion to deliver enduring results for our clients.

Not Specified
Principal Research Scientist - AI & Machine Learning
✦ New
🏢 Novateur Research Solutions
Salary not disclosed
Ashburn, VA 1 day ago

Principal Research Scientist – AI & Machine Learning

Novateur stands for Innovation. We value creativity, vision, collaboration, and above all, ambition to innovate. Novateur Research Solutions is an R&D firm located in Northern Virginia, developing intelligent systems that push the boundaries of computer vision, AI, and large-scale learning.

We are hiring a Principal Research Scientist to lead cutting-edge programs in AI, computer vision, and intelligent systems. This role offers leadership opportunities to define new research directions and shape next-generation technologies.


Responsibilities:

• Serve as PI or co-PI on government-funded R&D programs.

• Conceive, design, and oversee research in learning systems, spatiotemporal modeling, and geo-localization.

• Publish, present, and contribute thought leadership to the AI community.

• Mentor research staff and guide proposal development.


Requirements:

• PhD with 7+ years of research experience.

• Demonstrated leadership in ML, vision, or scientific computing.

• Record of funding, publications, and technical impact.

• U.S. Citizen or Permanent Resident.


Preferred:

• Experience with multimodal learning, uncertainty quantification, or causal inference.


Why Novateur?

Join a team that values creativity and initiative. At Novateur, you’ll lead transformative projects that redefine what’s possible in intelligent systems.


Company Benefits:

Novateur offers competitive pay and benefits comparable to Fortune 500 companies that include a wide choice of healthcare options with generous company subsidy, 401(k) with generous employer match, paid holidays and paid time off increasing with tenure, and company paid short-term disability, long-term disability, and life insurance.

We offer a work environment which fosters individual thinking along with collaboration opportunities within and beyond Novateur. In return, we expect a high level of performance and passion to deliver enduring results for our clients.

Not Specified
Instructor Pool - UX Design, UI Design, and UX Research - UC Berkeley Extension
✦ New
Salary not disclosed
San Francisco, CA 1 day ago
Position overview

Position title:
Instructor (Non-Senate, Non-Tenure Track)

Salary range:
The compensation model varies depending upon the course delivery format. For a synchronous Live Online course, a reasonable estimate for this position is $1,500 - $3,600 total per course. For an asynchronous Fixed Date Online course, this position is paid $150 - $170 per enrolled student and a reasonable estimate ranges from $1,200 - $3,400 total per course. Compensation may be shared among co-instructors depending upon the percentage of course content that each co-instructor teaches. Instructor compensation is determined by course length, number of units, enrollment, budgetary considerations, and other factors.

Percent time:
Part-time by agreement on a course-by-course basis.

Anticipated start:
Some appointments may begin as early as the spring semester.

Review timeline:
Applicants are considered for positions as needs arise; the existence of this applicant pool does not guarantee that a position is available. The applicant pool will remain in place for 9-12 months; those interested in remaining in the applicant pool beyond the advertised final closing date must reapply.

Position duration:
Length of courses differs depending on the subject, level, format/schedule, and credits taught. For the fall, spring, and summer semesters, course length typically ranges from approximately 6 to 12 weeks. Further course agreements may be assigned based upon program needs, meritorious performance, and funding availability.

Application Window


Open date: August 27, 2025




Next review date: Thursday, Mar 12, 2026 at 11:59pm (Pacific Time)

Apply by this date to ensure full consideration by the committee.




Final date: Wednesday, Aug 26, 2026 at 11:59pm (Pacific Time)

Applications will continue to be accepted until this date, but those received after the review date will only be considered if the position has not yet been filled.



Position description

UC Berkeley Extension (UNEX), the continuing education branch of the University of California, Berkeley, has been building bridges between UC Berkeley and the public since 1891. UNEX serves the professional and continuing education goals of thousands of people each year and plays an essential part of the University mission to: extend the research and scholarship of UC Berkeley to a global community; increase access to higher education for non-traditional, online, and international students; and improve the workforce. UC Berkeley Extension is a part of the division under the leadership of the Dean of Extended Education that also includes Berkeley Summer Sessions, Berkeley Study Abroad, and Osher Lifelong Learning Institute.



UC Berkeley Extension invites applications for a pool of qualified, dynamic instructors with a commitment to professional and continuing education in UX Design, UI Design, and UX Research to teach one or more online courses each year for our Arts and Humanities department.



Courses are offered online:




  • Online instruction is delivered asynchronously through our learning management system (Canvas) or through synchronous live lectures (Zoom).
  • Most synchronous live online lecture courses are offered in the evening and on the weekend (U.S.A. Pacific Time).


Course Subjects

We are seeking qualified applicants who possess current subject matter expertise and/or teaching knowledge in (but not limited to) the following course subjects. For program and course descriptions, please refer to the departmental link below.



User Experience and User Interface (UX-UI) Design




  • Accessibility in UX Design
  • Algorithmic Thinking & System Flows
  • Content Design
  • Diagramming and Prototyping for UX
  • Essentials of User Experience (UX) Design
  • Information Architecture
  • User-Interface (UI) Design
  • UX Design Portfolio
  • UX for Emerging Technologies: Augmented Reality (AR), Mixed Reality (MR), and Artificial Intelligence (AI)
  • UI for Emerging Technologies: Voice User Interface (VUIs)


User Research Methods




  • Qualitative User Research for UX
  • Quantitative User Research for UX


Other UX-UI Design and UX Research Related Topics

(please specify in your cover letter)



General Duties

The department seeks candidates who can support the success of all students through inclusive curriculum, classroom environment, and pedagogy. Specific duties and expectations will vary depending on the method of instruction including: Synchronous Live Online (Zoom) or Asynchronous Online (Fixed Date).




  • For synchronous instruction (live online courses), duties include but are not limited to: syllabus development; assignment development; lesson planning for class meetings; preparing and submitting required texts and course materials; reviewing and updating Canvas course site; and delivering lectures, presentations, and learning activities for all required hours of instruction.
  • For asynchronous instruction (fixed date online courses), duties include but are not limited to: reviewing the syllabus and pre-populated online course content; learning and utilizing Canvas classroom management tools; and requesting any training needs from the Program Director or Department Director.
  • For all instruction (regardless of course format) duties include but are not limited to: completing required trainings as mandated by the UC Presidential policies; responding to student questions and learning needs in a timely manner; grading student assignments and posting final student grades to the instructor portal in a timely manner; utilizing University-approved course support platforms including the Canvas Learning Management System, Zoom, Instructor Portal, Google Workspace, etc.; reviewing and following University and departmental policies, logistics, and other guidelines as published on the departmental Instructional Resource Site; and responding to other requests from the Program Director or Department Director in a timely manner.


UX-UI Design and UX Research Program and Courses: public/category/ ?method=load&certificateId=29918624&selectedProgramAreaId=11461&selectedProgramStreamId=15551



Qualifications

Basic qualifications (required at time of application)

  • Bachelor's degree or equivalent international degree required.


Additional qualifications (required at time of start)

  • 5 or more years of professional industry work experience since degree, or 5 or more years of teaching experience since degree.

  • U.S.A. Residency and U.S.A. Work Authorization: All work must be performed in the United States, whether in person or online. For applicants who are not US citizens or permanent residents, a valid US work authorization is required for the duration of employment. Applicants should not expect the department to sponsor a work visa on their behalf.


Preferred qualifications

  • Advanced degree in UX Design preferred.
  • 5 or more years of professional industry work experience in UX design, artificial intelligence (AI), voice design, web design or development, product design, graphic design, interaction design, human computer interaction, human ergonomics, computer science, engineering/programming, cognitive science, psychology, anthropology, or sociology.
  • Experience in User Research Methods (quantitative/qualitative).
  • Proficiency in design thinking methodologies and their application to user-centered design challenges.
  • Proficiency in one of the following for design tools: Figma, InVision, Miro, Mural, UXPin, or AI apps and plugins.
  • Proficiency in Augmented Reality (AR), Mixed Reality (MR) and Virtual Reality (VR)
  • Proficiency in one of the following for Voice User Interface (VUI) design courses: Voiceflow, Alexa Skill Kit (ASK), Action Builder (for Google Assistant), Mycroft, Web Speech API, etc.
  • Experience writing technical content and project specs.
  • Knowledge of existing and new technologies and constraints, including knowledge of artificial intelligence and its integration with user experience design.
  • Teaching, training or coaching experience in the course subject, within a U.S. corporate environment or at a U.S. college/university institution.
  • Experience in creating syllabi, learning objectives, lectures/presentations, learning activities, assignments, assessments, exams, and quizzes.
  • Experience teaching online and/or developing academic content for online courses.
  • Ability to convey conceptual and complex ideas and information.
  • Ability to support the success of all students through inclusive curriculum, classroom environment, and pedagogy.
  • Effective verbal/written communication and presentation skills (English).
  • Effective organizational skills with attention to detail.
  • Ability to collaborate with colleagues and work within a team environment
  • Proficiency in (or willingness to learn) instructional and other technology, such as: Learning Management Systems (Canvas); lecture/presentation capture applications (Panopto); online video conferencing (Zoom); Microsoft Office (Word and PowerPoint); file sharing (Google drive or Dropbox); and Google Workspace tools (email, calendar, docs, sheets, slides, etc).


Application Requirements

Document requirements

  • Curriculum Vitae - Your most recently updated C.V.


  • Cover Letter - In your cover letter, please include:

    1) the top 3 course subject(s) you are applying for within the UX-UI Design and/or User Research disciplines;

    2) a link to your professional website that includes your UX-UI Design and/or User Research portfolio with samples of your work; and

    3) please discuss prior teaching experience, teaching approach, and other/future UX-UI Design and/or User Research teaching interests. This can include, for example, specific efforts, accomplishments, and future plans to support the success of all students through inclusive curriculum, classroom environment, and pedagogy.




Reference requirements

  • References are requested from candidates at the interviewing stage, and references are only contacted for finalists.


Apply link:
JPF05003

Help contact:



About UC Berkeley

UC Berkeley is committed to diversity, equity, inclusion, and belonging in our public mission of research, teaching, and service, consistent with UC Regents Policy 4400 and University of California Academic Personnel policy (APM 210 1-d). These values are embedded in our Principles of Community, which reflect our passion for critical inquiry, debate, discovery and innovation, and our deep commitment to contributing to a better world. Every member of the UC Berkeley community has a role in sustaining a safe, caring and humane environment in which these values can thrive.



The University of California, Berkeley is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or protected veteran status.



For more information, please refer to the University of California's Affirmative Action and Nondiscrimination in Employment Policy and the University of California's Anti-Discrimination Policy.



In searches when letters of reference are required all letters will be treated as confidential per University of California policy and California state law. Please refer potential referees, including when letters are provided via a third party (i.e., dossier service or career center), to the UC Berkeley statement of confidentiality prior to submitting their letter.



As a University employee, you will be required to comply with all applicable University policies and/or collective bargaining agreements, as may be amended from time to time. Federal, state, or local government directives may impose additional requirements.


Unless stated otherwise, unambiguously, in the position description, this position does not include sponsorship of a new consular H-1B visa petition that would require payment of the $100,000 supplemental fee.



As a condition of employment, the finalist will be required to disclose if they are subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct.




  • "Misconduct" means any violation of the policies or laws governing conduct at the applicant's previous place of employment, including, but not limited to, violations of policies or laws prohibiting sexual harassment, sexual assault, or other forms of harassment or discrimination, as defined by the employer.
  • UC Sexual Violence and Sexual Harassment Policy
  • UC Anti-Discrimination Policy
  • APM - 035: Affirmative Action and Nondiscrimination in Employment


Job location
San Francisco Bay Area, California, U.S.A.
Not Specified
Instructor Pool - Clinical Research, Regulatory Affairs, and Biotechnology - UCBerkeley Extension
✦ New
🏢 University of California-Berkeley
Salary not disclosed
San Francisco, CA 1 day ago
Position overview

Position title:
Instructor (Non-Senate, Non-Tenure Track)

Salary range:
The compensation model varies depending upon the course delivery format. For a synchronous Live Online course, a reasonable estimate for this position is $1,500 - $4,500 total per course. For an asynchronous Fixed Date Online course, this position is paid $200 - $350 per enrolled student and a reasonable estimate ranges from $1,600 -$5,250 total per course. Instructor compensation is determined by course length, number of units, enrollment, budgetary considerations, and other factors.

Percent time:
Part-time by agreement on a course-by-course basis.

Anticipated start:
Some appointments may begin as early as the spring semester.

Review timeline:
Applicants are considered for positions as needs arise; the existence of this applicant pool does not guarantee that a position is available. The applicant pool will remain in place for 9-12 months; those interested in remaining in the applicant pool beyond the advertised final closing date must reapply.

Position duration:
Length of courses differs depending on the subject, level, format/schedule, and credits taught. For the fall, spring, and summer semesters, course length typically ranges from approximately 2 days to 8 weeks. Further course agreements may be assigned based upon program needs, meritorious performance, and funding availability.

Application Window


Open date: August 27, 2025




Next review date: Monday, Mar 23, 2026 at 11:59pm (Pacific Time)

Apply by this date to ensure full consideration by the committee.




Final date: Wednesday, Aug 26, 2026 at 11:59pm (Pacific Time)

Applications will continue to be accepted until this date, but those received after the review date will only be considered if the position has not yet been filled.



Position description

UC Berkeley Extension (UNEX), the continuing education branch of the University of California, Berkeley, has been building bridges between UC Berkeley and the public since 1891. UNEX serves the professional and continuing education goals of thousands of people each year and plays an essential part of the University mission to: extend the research and scholarship of UC Berkeley to a global community; increase access to higher education for non-traditional, online, and international students; and improve the workforce. UC Berkeley Extension is a part of the division under the leadership of the Dean of Extended Education that also includes Berkeley Summer Sessions, Berkeley Study Abroad, and Osher Lifelong Learning Institute.



UC Berkeley Extension invites applications for a pool of qualified, dynamic instructors with a commitment to undergraduate, professional, and continuing education in Clinical Research, Regulatory Affairs, and Biotechnology to teach one or more online courses each year for our Sciences, Mathematics, and Biotechnology department.



Courses are offered online:




  • Online instruction is delivered asynchronously through our learning management system (Canvas) or through synchronous live lectures (Zoom).
  • Most synchronous live online lecture courses are offered in the evening and on the weekend (U.S.A. Pacific Time).


Course Subjects

We are seeking qualified applicants who possess current subject matter expertise and/or teaching knowledge in (but not limited to) the following course subjects. For program and course descriptions, please refer to the departmental link below.



Clinical Research




  • Introduction to Clinical Research: Clinical Trial Phases and Design
  • Clinical Trial Planning: Protocol Development, Data Management and Clinical Site Activities
  • Clinical Trial Implementation: Site Initiation, Subject Recruitment, Monitoring and Safety Reporting
  • Clinical Trial: Data Analysis, Regulatory Audits, Vendor Selection and Project Management


Regulatory Affairs




  • Principles of Regulatory Affairs: Pharmaceuticals and Medical Devices
  • Submissions and Commercialization
  • Preparation, Submission and Agency Interfacing
  • Harmonization Across Worldwide Applications
  • Post-Approval Activities
  • Principles of Supply Chain and Manufacturing
  • Principles of Product and Process Development
  • Principles of Quality and Compliance
  • Regulatory Compliance for Pharmaceutical Products


Other Biotechnology Courses




  • Drug Development Process
  • Other Biotechnology course topics (please specify in your cover letter)


Teaching Experience




  • Classroom Teaching Experience
  • Synchronous Online Teaching Experience (online lectures via Zoom)
  • Asynchronous Online Teaching Experience (via learning management system)


General Duties

The department seeks candidates who can support the success of all students through inclusive curriculum, classroom environment, and pedagogy. Specific duties and expectations will vary depending on the method of instruction including: Synchronous Live Online (Zoom) or Asynchronous Online (Fixed Date).




  • For synchronous instruction (live online courses), duties include but are not limited to: syllabus development; assignment development; lesson planning for class meetings; preparing and submitting required texts and course materials; reviewing and updating Canvas course site; and delivering lectures, presentations, and learning activities for all required hours of instruction.
  • For asynchronous instruction (fixed date online courses), duties include but are not limited to: reviewing the syllabus and pre-populated online course content; learning and utilizing Canvas classroom management tools; and requesting any training needs from the Program Director or Department Director.
  • For all instruction (regardless of course format) duties include but are not limited to: completing required trainings as mandated by the UC Presidential policies; responding to student questions and learning needs in a timely manner; grading student assignments and posting final student grades to the instructor portal in a timely manner; utilizing University-approved course support platforms including the Canvas Learning Management System, Zoom, Instructor Portal, Google Workspace, etc.; reviewing and following University and departmental policies, logistics, and other guidelines as published on the departmental Instructional Resource Site; and responding to other requests from the Program Director or Department Director in a timely manner.


Clinical Research Conduct and Management Program: public/category/ ?method=load&certificateId=17168&selectedProgramAreaId=15498&selectedProgramStreamId=15604

Regulatory Affairs Program: public/category/ ?method=load&certificateId=17180

Clinical Research, Regulatory Affairs, and Biotechnology Courses: academic-areas/sciences-and-biotechnology/?nav=5#!?tab=courses&programStream=Life%20Science%20Business%20and%20Biotechnology



Qualifications

Basic qualifications (required at time of application)

  • Advanced degree


Additional qualifications (required at time of start)


  • U.S.A. Residency and U.S.A. Work Authorization: All work must be performed in the United States, whether in person or online. For applicants who are not US citizens or permanent residents, a valid US work authorization is required for the duration of employment. Applicants should not expect the department to sponsor a work visa on their behalf.


Preferred qualifications

  • Doctorate degree or equivalent international degree in course subject.
  • 3 or more years of teaching, training, or coaching experience in the course subject at a U.S. college/university institution, or within a U.S. Clinical Research, Regulatory Affairs, or other Biotechnology corporate environment.
  • Knowledge of federal and California state laws and regulations as applicable to the course subject.
  • Professional license, certification, or credential within a Clinical Research, Regulatory Affairs, or other Biotechnology field.
  • Experience in creating syllabi, learning objectives, lectures/presentations, learning activities, assignments, assessments, exams, and quizzes.
  • Experience teaching and/or developing academic content for online courses.
  • Ability to convey conceptual and complex ideas and information.
  • Ability to support the success of all students through inclusive curriculum, classroom environment, and pedagogy.
  • Effective verbal/written communication and presentation skills (English).
  • Effective organizational skills with attention to detail.
  • Ability to collaborate with colleagues and work within a team environment.
  • Proficiency in (or willingness to learn) instructional and other technology, such as: Learning Management Systems (Canvas); lecture/presentation capture applications (Panopto); online video conferencing (Zoom); Microsoft Office (Word and PowerPoint); file sharing (Google drive or Dropbox); and Google Workspace tools (email, calendar, docs, sheets, slides, etc).


Application Requirements

Document requirements

  • Curriculum Vitae - Your most recently updated C.V.


  • Cover Letter - Please discuss prior teaching experience, teaching approach, and other/future teaching interests. This can include, for example, specific efforts, accomplishments, and future plans to support the success of all students through inclusive curriculum, classroom environment, and pedagogy.




Reference requirements

  • References are requested from candidates at the interviewing stage, and references are only contacted for finalists.


Apply link:
JPF04761

Help contact:



About UC Berkeley

UC Berkeley is committed to diversity, equity, inclusion, and belonging in our public mission of research, teaching, and service, consistent with UC Regents Policy 4400 and University of California Academic Personnel policy (APM 210 1-d). These values are embedded in our Principles of Community, which reflect our passion for critical inquiry, debate, discovery and innovation, and our deep commitment to contributing to a better world. Every member of the UC Berkeley community has a role in sustaining a safe, caring and humane environment in which these values can thrive.



The University of California, Berkeley is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or protected veteran status.



For more information, please refer to the University of California's Affirmative Action and Nondiscrimination in Employment Policy and the University of California's Anti-Discrimination Policy.



In searches when letters of reference are required all letters will be treated as confidential per University of California policy and California state law. Please refer potential referees, including when letters are provided via a third party (i.e., dossier service or career center), to the UC Berkeley statement of confidentiality prior to submitting their letter.



As a University employee, you will be required to comply with all applicable University policies and/or collective bargaining agreements, as may be amended from time to time. Federal, state, or local government directives may impose additional requirements.


Unless stated otherwise, unambiguously, in the position description, this position does not include sponsorship of a new consular H-1B visa petition that would require payment of the $100,000 supplemental fee.



As a condition of employment, the finalist will be required to disclose if they are subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct.




  • "Misconduct" means any violation of the policies or laws governing conduct at the applicant's previous place of employment, including, but not limited to, violations of policies or laws prohibiting sexual harassment, sexual assault, or other forms of harassment or discrimination, as defined by the employer.
  • UC Sexual Violence and Sexual Harassment Policy
  • UC Anti-Discrimination Policy
  • APM - 035: Affirmative Action and Nondiscrimination in Employment


Job location
San Francisco Bay Area, California, U.S.A.
Not Specified
Google Ads Specialist (Lead Generation - Home Services)
✦ New
Salary not disclosed
Metro Detroit, MI 1 day ago


Google Ads Lead Generation Specialist – Home Services (Remote)


World of Floors is a well established flooring company based in the Detroit Metro area, specializing in Shop-At-Home flooring sales.

We are seeking an experienced Google Ads specialist who understands lead generation marketing for local service businesses.

Our goal is simple: generate qualified in-home flooring estimate requests at a profitable cost per lead.

This is NOT a social media role. This position focuses strictly on high-intent search traffic.


Responsibilities

• Build and manage Google Search campaigns for flooring installation

• Keyword research and expansion

• Negative keyword management

• Bid management and budget optimization

• Conversion tracking setup (calls + form submissions)

• Weekly performance reporting

• Landing page optimization recommendations


Performance Targets

• Maintain cost per lead

• Generate 150+ estimate requests per month

• Maintain strong Quality Scores across campaigns


Requirements

• 3+ years Google Ads experience

• Proven lead generation campaign results

• Experience with call tracking and conversion tracking

• Strong English communication


Compensation

$1,500 – $2,000/month depending on experience.

Please include:

  1. Screenshots of campaign performance you have managed
  2. Example cost per lead results
  3. Description of campaign structure used
Not Specified
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