Accel Research Sites is looking for a Clinical Research Source Development Coordinator to support source document requirements for clinical trials. This role will involve creating and maintaining documentation that follows industry guidelines. The ideal candidate will have at least 1 year of experience in clinical research and a knack for detail-oriented tasks.Responsibilities include ensuring that necessary documents are prepared accurately for each trial and maintaining communication with various stakeholders. A supportive environment with comprehensive employee benefits awaits you.#J-18808-Ljbffr
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