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Clinical Research Coordinator - Los Angeles, United States - Resourceful Talent Group
Description
We are seeking a dedicated and experienced Clinical Research Coordinator (CRC) with a specialization as an Investigational Product (IP) designee.
Responsibilities:
Coordinate and oversee all aspects of clinical trials as an IP designee.
Prepare and manage investigational products according to protocol requirements.
Ensure compliance with all federal, state, and local regulations, as well as ethical standards pertaining to clinical research.
Work closely with medical staff and other departments to ensure trials are conducted safely and effectively.
Maintain accurate documentation and records of trial activities.
Communicate with regulatory bodies and sponsors as required.
Proven experience as a Clinical Research Coordinator.
Certification or proven experience as an IP designee is essential.
Former experience in medical assistance or nursing is highly desirable.
Strong understanding of regulatory requirements and clinical trial management.
Excellent organizational skills and attention to detail.
Ability to travel as required by the clinical study needs.
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