Clinical Research Coordinator

LeadStack Inc. is an award-winning, one of the nation's fastest-growing, certified minority-owned (MBE) staffing services provider of contingent workforce. As a recognized industry leader in contingent workforce solutions and Certified as a Great Place to Work, we're proud to partner with some of the most admired Fortune 500 brands in the world.

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 (phone number removed) or send an email on

Thanks and Regards

Akarsh Yathiraj

Senior Recruiter

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(phone number removed)

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611 Gateway Blvd, Ste 120

South San Francisco, CA 94080

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