Manager, Document Quality Reviewer

Independently performs DQR of clinical components of assigned documents (e.g., protocols, clinical study reports, investigator brochures, manuscripts, summary documents, regulatory responses, etc.). Formally documents quality review findings for assigned documents. Identifies and immediately escalates any significant findings. Participates in resolution of findings with the document authors, clinicians and other team members, if necessary. Manages DQR document archival processes and procedures. Independently produces style guides, manuals, and quality review work guides for Vaccine programs and documents, coordinating agreement on style issues within and across projects. Leads and/or manages the completion of complex tasks by applying technical skills and specialized knowledge to communicate initial findings. Analyzes DQR findings to identify root causes of errors and discrepancies and participate in corrective action planning. Leads the compilation and analysis of data quality metrics to ensure consistency of reviews. Participates on project teams, task forces, and/or working groups and develops recommendations for cross-Pfizer processes to ensure alignment with quality goals and other groups performing the same function.

According to JobzMall, the average salary range for a Manager, Document Quality Reviewer in 401 N Middletown Rd, Pearl River, NY 10965, USA is between $60,000 and $90,000 per year. This salary range depends on experience, job responsibilities, skill set, and the particular employer.

Pfizer Inc. is an American multinational pharmaceutical corporation headquartered in New York City, with its research headquarters in Groton, Connecticut. It is one of the world's largest pharmaceutical companies.