Clinical research coordinator
Location
San Francisco, CA | United States
Job description
Job Title: Clinical Research Coordinator
Locations: San Francisco, CA 94158 - Hybrid (3x/per week onsite)
Duration: 6 months contract
Rate : $35/hr - $40/hr on W2
Shift: M-F, 8:00 AM - 4:30 PM PST
Job Description:
- Study activity coordination and administrative study management experience are required.
- Fluency in the usage of Committee of Human Research (CHR) online iRIS system for submission, renewal, and modification of protocols through this system preferred.
- Clinical research associate preferred.
- Incumbent will provide clinical research coordination for a variety of health policy and clinical outcomes studies as assigned.
- The CRC will be responsible for recruiting study participants through screening in person and Epic.
- The CRC will collect data as required by study protocols from the established participants.
- The CRC will assist with IRB submission and other regulatory documentation maintenance needed for each study supported.
Key Responsibilities:
- The incumbent will work under the direction of their supervisor in support of Department PI.
- The selected individual will play a critical role in coordinating aspects of clinical research daily operations on assigned studies within the Department of Orthopaedic Surgery.
- The Clinical Research Coordinator (CRC) will ensure successful implementation of and adherence to clinical research protocols regarding planning, administration, timeline management enrollment, participant engagement data collection and reporting.
- The CRC will demonstrate competence in clinical research skills, problem solving, priority setting and serve as a resource for others in the department for all aspects of conducting a clinical trial.
- This requires close interaction with patient care staff, research team members and study personnel at other sites.
- Study duties include the coordination of research protocols, including coordination of the data/specimen collection and operations of several concurrent clinical research studies under the guidelines of research protocols, regulating agency policies.
- This includes but is not limited to collecting and reporting on study results; create, clean, update, and manage databases and comprehensive datasets and reports.
- Critical duties include preparation, coordination and/or maintenance of regulatory documentation in the CHR system as well as all other reporting / compliance requirements.
To know more about current opportunities at LeadStack, please visit us at
Should you have any questions, feel free to call me on (415) 322-5419 or send an email on [email protected]
Job Type: Contract
Salary: $30.00 - $40.00 per hour
Schedule:
Work Location: In person
Job tags
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