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Job Details


PRA Health Sciences

Clinical Research Coordinator I

Pharmaceuticals

All

Yearly

No

Silver Spring, Maryland, United States

Duties/Responsibilities:

  • Participates in the design, administration and monitoring of clinical trials.
  • Analyzes and evaluates clinical data gathered during research.
  • Ensures compliance with protocol and overall clinical objectives.
  • Relies on instructions and pre- established guidelines to perform the functions of the job.
  • Works under immediate supervision.
  • Primary job functions do not typically require exercising independent judgment.

Qualifications:

  • Requires a BS, RN, or BSN degree or equivalent.
  • Minimum of 1 year of experience in the field or in a related area.
  • Knowledge of FDA regulatory requirements is required.
  • Has knowledge of commonly-used concepts, practices, and procedures within a particular field.

ICON Government and Public Health Solutions specializes in preclinical through phase IV support of clinical research and clinical trial services for biologics, drugs, and devices. We help our customers get their products to market faster with a wide array of research, regulatory, and sponsor services both within the US and around the globe and respond rapidly to global health crises.