Remote Clinical Study Coordinator

A leading clinical research organization is seeking a qualified candidate to communicate with site teams, handle document submissions, and support recruitment activities. The role requires a Bachelor's degree and a minimum of 2 years of relevant experience. Key responsibilities include managing site communications, performing data entry, and maintaining documentation according to IRB/FDA standards. Ideal candidates will have strong critical thinking and communication skills, with the ability to work both independently and as part of a team.

This position is based in the United States.
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