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The Document Review Specialist is responsible for reviewing Informed Consent Forms and patient recruiting materials to ensure compliance with regulatory requirements and GCP guidelines. They also manage the filing of documentation in TMF/eTMF and provide input for CAPA activities related to document review.
Job Overview:
Document Review Specialist I is responsible for reviewing Informed Consent Forms and Advertisements following project and country specific regulations as well as ICH-GCP, FDA and other regional guidance. Document Review Specialist I may responsible for reviewing revised protocols and core ICF’s.
Summary of Responsibilities:
Qualifications (Minimum Required):
Experience (Minimum Required):
Preferred Qualifications Include:
Physical Demands/Work Environment:
Learn more about our EEO & Accommodations request here.
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