Medical QC Editor
Fortrea
3 - 5 years
Bengaluru
Posted: 25/02/2026
Job Description
Job Overview:
Responsible for reviewing clinical study reports, patient safety narratives, appendices, informed consent forms, clinical protocols, and amendments to ensure documents are accurate, consistent, grammatically correct, well written, and logical by providing review comments and documentation to the Writer.
Summary of Responsibilities:
- Ensures consistency and accuracy of clinical study reports, patient safety narratives, appendices, informed consent forms, clinical protocols, and amendments to source documents, templates, and client requirements.
- Completes reviews and checklists within given timelines.
- Collaborates with writers to discuss discrepancies, omissions, and errors.
- Understands the task to be completed and the budgeted hours.
- Participates in staff meetings, client meetings, and project team update meetings as appropriate.
- Reviews and assists in department template updates.
- Performs any other duties as assigned by Manager or Supervisor.
- And all other duties as needed or assigned
Qualifications (Minimum Required):
- Associate degree or Bachelor of Science/Arts (BS/BA) degree.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
- Ability to understand and perform basic mathematical computations.
- Understanding of medical, pharmacokinetic, and statistical principles.
Experience (Minimum Required):
- 3 years of clinical research experience.
- Minimum 3 years of experience at Associate Medical QC Editor level.
- Must have excellent command of the English language, both oral and written. This includes knowledge of standard editing and proofing conventions, grammar, sentence structure, and style.
- Ability to efficiently use basic software (e.g., Word, Excel, PowerPoint).
Preferred Qualifications Include:
- High level of attention to detail and specifics.
- Knowledge of medical terminology preferred.
Physical Demands/Work Environment:
- Home based environment
Learn more about our EEO & Accommodations request here.
About Company
Fortrea is a leading global Contract Research Organization (CRO) that provides comprehensive clinical development and consulting services to pharmaceutical, biotechnology, and medical device companies. Spun off from Labcorp in 2023, Fortrea specializes in managing clinical trials from early-phase research to late-stage development. With a global footprint, the company supports the development of new therapies by offering services in clinical trial management, regulatory consulting, data management, and more. Its mission is to help bring innovative, life-saving treatments to market faster and more efficiently.
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