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Clinical Research Associate

A clinical research associate is responsible for developing and writing trial protocols; presenting trial protocols to a steering committee; designing data collection forms known as case record forms (CRFs); coordinating with the ethics committee that safeguards the rights, safety, and well being of all trial subjects; and managing regulatory authority applications and approvals. A clinical research associate is also responsible for locating and assessing the appropriateness of facilities at a study center. Briefing doctors/ consultants on conducting of a trial and setting up the study centers is part of responsibilities.

A clinical research associate should be a graduate with a degree in life sciences or chemical sciences. Experience in the field of clinical research is preferred for most positions. A clinical research associate job often requires building effective relationships with trial center staff and colleagues. Ability to multi task, and have good organizational, IT, and administrative skills is also essential.

Search related to:

Clinical Research Manager
Clinical Research Scientist

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