Sqrl Jobs in Usa
5 positions found
Highlights
- $65,000 - $89,000 annual salary based on experience
- Great benefits including 401k w/match and 15 days PTO
- Consistent schedule, no overnights or weekends
- Work with cutting edge oncology research trials
About Our Client
Our client is a fast growing site network that currently has over 30 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors.
Responsibilities
As a CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process!
- Conduct procedures such as vital signs, blood draws, EKGs, and scans.
- Patient recruitment, enrollment, scheduling, and consent
- Lab procedures and shipments
- Maintain GCP and follow protocols
- Data management in EDC systems
- Overall coordination of the study from start up to close out
- Focus on oncology based research studies
Qualifications:
- 2+ years of experience working as a CRC on sponsor backed clinical trials
- Phlebotomy and lab processing experience (ability to perform without supervision)
- Ability to work on site M-F on site (there is no remote or hybrid days) and be flexible for some later or longer shifts
- Experience working with Oncology clinical trials
Highlights
- Play a key role in helping patients get involved in clinical trials
- up to $21 - $30 an hour + full benefits
- Growth opportunities to CRC, Sr. CRC, and more!
- Great stepping stone into research, or a way to get more experience!
As an Clinical Research Assistant, you will be integral to the success of our research endeavors, providing essential support throughout all phases of clinical trials. Key responsibilities include:
- Assist in Start-up and Implementation Activities: Collaborate with the research team to facilitate the initiation of new studies, including protocol development and regulatory submissions.
- Completion and Submission of Clinical Trials Amendments: Ensure timely completion and accurate submission of all amendments to the Institutional Review Board (IRB), adhering to regulatory guidelines and protocols.
- Editing Informed Consent Documents: Review and edit informed consent documents to ensure clarity, accuracy, and compliance with regulatory standards.
- Correspondence with Stakeholders: Serve as a primary point of contact for communication with the IRB, investigators, and sponsors throughout the clinical trial process, maintaining open lines of communication and addressing inquiries promptly.
- Preparation of Annual Progress Reports: Compile and prepare comprehensive progress reports for IRB renewal of ongoing studies, summarizing key findings and milestones achieved.
- Collection and Submission of Regulatory Documents: Facilitate the collection, completion, and submission of regulatory documents to various regulatory entities, ensuring compliance with regulatory requirements.
- Maintenance of Regulatory Binders: Establish and maintain regulatory binders and other relevant files, organizing documentation meticulously during the review, approval, and activation process for clinical trials.
- Coordination of Safety Reports: Coordinate the review and processing of safety reports to the IRB, ensuring prompt reporting and appropriate follow-up actions as required.
Qualifications:
- Bachelor's degree in a relevant field (e.g., life sciences, healthcare administration, or related discipline) preferred.
- Prior experience in clinical research or healthcare administration is preferred.
- Experience with Phlebotomy, EKG, taking Vitals, etc. REQUIRED
- Strong attention to detail and organizational skills.
- Excellent written and verbal communication abilities.
- Familiarity with regulatory requirements governing clinical research (e.g., FDA regulations, ICH-GCP guidelines) is desirable.
Highlights
- $120k-$150k + bonus/commission + equity + Great benefits
- Pharmaceutical Sales role in a high-growth CNS/psychiatry portfolio
- Call on Psychiatry, Hospitals, PCPs, Neurology
- The company has grown significantly over the last 5 years, increasing its publicly traded valuation over 800% in that time - due to strong pipeline and launch execution
The Company
We’re partnering with an innovative biopharmaceutical organization building a modern, digitally enabled commercial model within psychiatry and CNS. This is a front line sales role for proven pharmaceutical or medical device sales reps excited to work with exciting new CNS products and launch new indications.
The Role
Execute commercial activities for assigned geography, establish relationships with customers, and ensure successful promotion of assigned product. This role is field-based and will require gaining access to customers in a clinic or hospital setting while also maximizing the ability to engage through digital channels.
You will be responsible for product performance at a territory level and expected to be a disease category expert and product champion. You will provide account management support and exhibit business knowledge of the local landscape to assess key stakeholders plus future trends within the marketplace!
Job Responsibilities and Duties include:
- Proficient in both virtual and live customer engagements
- Develop a comprehensive and effective territory business plan aimed at achieving and exceeding quarterly & annual goals established by commercial leadership
- Develop strong customer relationships by better understanding the customer’s needs
- Serve as a resource/consultant to customers and staff regarding payer policies and processes (i.e., eligibility and benefit verification, prior-authorization, and appeals/denials)
- Maximize use of marketing resources to maintain and develop customer relationships for the purpose of growing the customers’ confidence to prescribe medications for appropriate patients
- Provide feedback to sales and commercial leadership, colleagues, marketing, and other internal departments about changing environment and results
Qualifications
- 2+ years of pharmaceutical/biotech field sales
- Candidates with recent psychiatry/CNS sales experience
- Proven performance in sales
- Product launch experience strongly preferred
- Must reside within the assigned geography
Highlights:
- Salary: $75,000 - $90,000 based on Exp
- Full Benefits
- Mon - Fri Schedule; fully on on site
- Studies in allergy, asthma, vaccines, and more!
Our Client:
We are working with an exciting clinical trial site organization with over 25 locations, dedicated to advancing innovative therapies and improving lives by making clinical research more efficient and accessible. They focus on on large-volume recruitment and retention of diverse and specialty patient populations, and have an experienced team with extensive physician partnerships help deliver high-quality data across a wide range of therapeutic areas!
The Role:
We are seeking an experienced CRC that values strong operations, thoughtful study execution, and team-based approach to clinical research!
- Coordinate all aspects of assigned clinical trials from site initiation through close-out
- Conduct subject visits and ensure accurate, timely documentation in compliance with all applicable standards
- Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
- Manage subject recruitment, informed consent, and retention activities (There is a recruitment team to support day to day recruitment)
- Ensure timely EDC data entry and resolution of queries
- Report and follow up on AEs, SAEs, and protocol deviations
- Collaborate with investigators, sponsors/CROs, labs, and internal teams
- Prepare for and participate in monitoring visits, audits, and inspections
- Maintain regulatory documentation and ensure training compliance for amendments and systems
- Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)
- Attend investigator meetings and provide cross-functional support as needed
- Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory
Requirements:
- 3+ years exp as a CRC on sponsor backed trials
- Ability to work on site M-F (NO hybrid or remote days)
Highlights:
- Great opportunity for PIs/Research Physicians to add additional hours or more research!
- $140 - $160/hr; 20 hours/week
- Direct employment (W2)
- Studies in pre-diabetes, type 1 and type 2 diabetes, obesity, NAFLD/MASH, and vaccines
Our Client:
We are working with an exciting clinical trial site organization with over 25 locations, dedicated to advancing innovative therapies and improving lives by making clinical research more efficient and accessible. They focus on on large-volume recruitment and retention of diverse and specialty patient populations, and have an experienced team with extensive physician partnerships help deliver high-quality data across a wide range of therapeutic areas!
The Role:
- Lead and oversee clinical trials by ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
- Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team
- Participate in investigator meetings and educational initiatives
- Obtain IRB approval for study initiation and any protocol modifications
- Oversee subject safety, trial conduct compliance, and the informed consent process.
- Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership
- Provide ongoing training and support to research staff
Requirements:
- Active and unrestricted license to practice as an MD or DO in CA
- Board-certified or board-eligible
- Communication and leadership skills, excitement to collaborate with sponsors, research teams, and external stakeholders
- Ability to work on site in Escondido, CA
