Sr. Clinical Data Coordinator
TradeJobsWorkForce90082 Los Angeles, CA, USFull-time
Clinical Data Coordinator Job Duties: Support laboratory data management procedures including authoring and reviewi... Show more
Clinical Research CoordinatorAvispa Technology • Los Angeles, CA, US
No longer accepting applications
Clinical Research Coordinator
Avispa Technology • Los Angeles, CA, US
12 days ago
Salary
$65.00 hourly
Job type
- Full-time
- Temporary
Job description
Clinical Research Coordinator 3359023 * Hourly pay: $65/hr * Worksite: Leading medical institution (Los Angeles, CA 90024 - Onsite) * W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL * 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: * 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. * Monitor study progress, identify and resolve operational issues, maintain regulatory documentation, and support regulatory submission processes and study compliance activities. * Mentor, train, supervise, and provide guidance to research coordinators and research staff on study procedures, policies, workflows, and clinical research best practices. * Develop, implement, and maintain SOPs, study manuals, workflows, and process improvement initiatives to enhance research quality, compliance, and operational efficiency. * 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: * 3+ years of Clinical Research Coordinator experience. * 1+ year of experience in a Senior Clinical Research Coordinator, Lead CRC, or equivalent leadership role. * Advanced knowledge of Good Clinical Practice (GCP), FDA regulations, and clinical research regulatory requirements. * Experience mentoring, training, and supervising research staff. * Experience with regulatory submissions and compliance processes. * Experience with Phase I-IV clinical trials is preferred. * Experience with Interventional and observational studies is preferred. * NIH and multicenter trial experience are preferred. * Experience working within an academic medical center environment is preferred. * Experience in academic medical centers and exposure to diverse clinical trial portfolios are preferred. Shift: * 08:00 am to 5:00 pm. (H)
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Clinical Research Coordinator • Los Angeles, CA, US
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