Job description
Piper Companies is actively seeking a Document Quality Reviewer to join a Vaccines Clinical Research & Development group. The Document Quality Reviewer will work remotely and work a traditional work schedule, and must be able to work East Coast hours.
Responsibilities for the Document Quality Reviewer:
- Complete data checking and clinical editing on components of assigned documents such as: protocols, clinical study reports, investigator brochures, regulatory responses, etc.
- Document quality review findings appropriately and escalate significant findings as needed.
- Partner with document authors, clinicians and other team members on resolution of findings as necessary
Qualifications for the Document Quality Reviewer:
- BS/BA degree in a related field. Advanced degree is a plus, but not necessary.
- 4+ years of experience in clinical/medical editing or quality review of clinical documents
- Knowledge of Microsoft Office and ability work independently
Compensation for the Document Quality Reviewer:
- Hourly Rate: $50-$60/hr, based on previous experience
- Benefits: medical, dental, vision, 401K
Keywords: document review, quality review, document quality review, clinical documents, clinical data checking, consistency checking, clinical editing, protocols, clinical study reports, clinical editing, medical editing, pharmaceutical, healthcare
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