Job Responsibilities : Document Quality Reviewer (contract)
Salary : $59000 per year
Company : Pfizer
Location : Remote US
The Document Quality Reviewer will conduct a document quality review (QDR) on the clinical components of documents authored by Vaccine Clinical Research & Development (VCRD). QDR includes clinical data checking, consistency checking, and clinical editing according to Pfizer and VCRD clinical guidelines.
Independently performs DQR (data checking and clinical editing) of clinical components of assigned documents; (eg, protocols, clinical study reports, investigator brochures, manuscripts, summary documents, regulatory responses)
Formally documents quality review findings for assigned documents. Identifies and immediately escalates significant findings
Participates in the resolution of findings with the document authors, clinicians, and other team members, if necessary
Stores DQR documentation in the departmental electronic archive.
Works on additional/special projects, as needed
BS/BA degree (preferably in English/Journalism/Communications or Biological Science). Advanced degree with relevant clinical/medical editing or document quality review experience
Minimum 4+ years of experience in clinical/medical editing and/or DQR/QC of clinical documents in the pharmaceutical/healthcare industry
Please note contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third-party payrolling partner.