Location
madrid, kingdom of spain, Spain
Posted
July 27, 2026
Job Description
Job Responsibilities Perform QC review of documents (e.G., clinical study protocols and amendments, clinical study reports (CSRs), Investigator’s Brochures, and Module 2 clinical summary documents) to ensure compliance with the client Style Guide and submission standards. Verify data in documents against the source tables, figures, and listings and format tables according to client standards. Copyedit/proofread clinical documents for grammar, style, and formatting according to AMA and the client style guides. Ensure internal consistency and confirm that data are reported correctly;
statements accurately reflect source documents or data (e.G., SAS tables and listings). Check reference lists in documents, verifying citation information versus Pub Med, ordering copies of references, adding them to the electronic document management system (EDMS), and ensuring each reference is cross‑referenced in the document. Proofread documents against the standard templates to ensure compliance ...
statements accurately reflect source documents or data (e.G., SAS tables and listings). Check reference lists in documents, verifying citation information versus Pub Med, ordering copies of references, adding them to the electronic document management system (EDMS), and ensuring each reference is cross‑referenced in the document. Proofread documents against the standard templates to ensure compliance ...