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Hiring Document Specialist II (TMF / eTMF)
🏢 Fortrea
🌐 Remote / Hybrid
🎓 Life Sciences / Pharmacy
📂 TMF / Documentation
Fortrea is hiring Document Specialist II for clinical documentation, TMF management, and regulatory compliance roles.
👉 Learn clinical research basics: Clinical Research Career Guide
📘 Understand CDISC & documentation: CDISC Guide
📋 Job Overview
- Role: Document Specialist II
- Company: Fortrea
- Location: Remote India (Bangalore / Pune / Mumbai)
- Experience: Freshers – 2 Years
- Qualification: Life Sciences / Pharmacy
- Industry: Clinical Research / CRO
- Job Type: Full-Time
- Salary: ₹3.5 – ₹6.5 LPA
📌 Key Responsibilities
- Maintain Trial Master File (TMF)
- Organize and archive clinical documents
- Ensure SOP and regulatory compliance
- Perform document QC checks
- Track missing documents
- Support TMF setup and closeout
- Generate tracking tools (Excel logs)
- Handle eTMF uploads and systems
- Support audit readiness
- Assist in mentoring junior staff
📊 Learn systems: Clinical Data vs SAS
🎯 Required Skills
- Documentation management
- MS Office & Adobe Acrobat
- Attention to detail
- Communication skills
- Multitasking ability
🧠 Practice aptitude: Logical Reasoning Quiz
🎓 Eligibility
- B.Pharm / M.Pharm / BSc / MSc
- Freshers – 2 years experience
- Knowledge of clinical trials preferred
- eTMF knowledge (Veeva etc.) is a plus
💰 Salary & Benefits
- ₹3.5 – ₹6.5 LPA
- Remote / hybrid flexibility
- Global clinical exposure
- Career growth in TMF & clinical operations
⚠️ Update: The application link for this opportunity has expired / is currently unavailable. We will update the post once a new application link becomes available.
🚀 Apply Now
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📌 Note Before You Apply:
Understand TMF, documentation workflows, and compliance basics.
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