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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.

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