Clinical Research Coordinator 3359023
- Hourly pay: $65/hr
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Worksite: Leading medical institution (Los Angeles, CA 90024 - Onsite)
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W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL
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40 hours/week, 3 Month Assignment (With possibility of extension)
A leading medical institution is seeking a Clinical Research Coordinator to oversee the day-to-day conduct of clinical research studies while ensuring compliance with sponsor, institutional, and regulatory requirements. This role provides operational leadership, mentorship, and oversight of research activities across a diverse portfolio of clinical trials.
Clinical Research Coordinator Responsibilities:
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Oversee daily operations of multiple clinical research studies, ensuring compliance with sponsor, institutional, FDA, GCP, and regulatory requirements throughout study start-up, maintenance, monitoring, and close-out activities.
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Monitor study progress, identify and resolve operational issues, maintain regulatory documentation, and support regulatory submission processes and study compliance activities.
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Mentor, train, supervise, and provide guidance to research coordinators and research staff on study procedures, policies, workflows, and clinical research best practices.
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Develop, implement, and maintain SOPs, study manuals, workflows, and process improvement initiatives to enhance research quality, compliance, and operational efficiency.
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Collaborate with investigators, sponsors, monitors, and research teams to support Phase I-IV, industry-sponsored, investigator-initiated, NIH-sponsored, interventional, observational, multicenter, and academic medical center research studies.
Clinical Research Coordinator Qualifications:
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3+ years of Clinical Research Coordinator experience.
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1+ year of experience in a Senior Clinical Research Coordinator, Lead CRC, or equivalent leadership role.
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Advanced knowledge of Good Clinical Practice (GCP), FDA regulations, and clinical research regulatory requirements.
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Experience mentoring, training, and supervising research staff.
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Experience with regulatory submissions and compliance processes.
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Experience with Phase I–IV clinical trials is preferred.
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Experience with Interventional and observational studies is preferred.
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NIH and multicenter trial experience are preferred.
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Experience working within an academic medical center environment is preferred.
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Experience in academic medical centers and exposure to diverse clinical trial portfolios are preferred.
Shift:
(H)
