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✅ eTMF Document Specialist Job – eClinical Solutions
🏢 Company: eClinical Solutions
📍 Location: Bangalore (Onsite)
🎓 Eligibility: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences, CS
🧪 Experience: 2 – 3 Years
📝 Job Type: Full-Time | TMF Document Management | Clinical Trials
🔎 Verified: ✅ Verified Job via Medical Jobs India – hitechplus.in
🧬 About eClinical Solutions
eClinical Solutions empowers life sciences organizations to run digital clinical trials with their elluminate® Clinical Data Cloud. With a global presence and innovative analytics, eClinical supports faster, smarter decisions in clinical research.
📄 Job Overview – QC Specialist (eTMF Document Specialist)
- 📌 Role: TMF QC Specialist
- 📌 Industry: Clinical Trials / CRO
- 📌 Location: Bangalore, Karnataka
🧑💼 Key Responsibilities
- Perform QC review of TMF documents per ICH-GCP, FDA, and EMA guidelines.
- Verify metadata, document indexing, and versioning in eTMF systems (e.g. Veeva, Trial Interactive).
- Identify gaps or discrepancies and coordinate with study teams and vendors.
- Support audit-readiness and TMF health report generation.
- Mentor junior QC associates and ensure SOP adherence.
✅ Eligibility & Skills
- 2–3 years experience in pharma/biotech, ideally in eTMF/document control roles.
- Degree in Life Sciences / Computer Science or related.
- Working knowledge of DIA TMF RM, 21 CFR Part 11, and eTMF platforms.
- Strong eye for detail, MS Office proficiency, and documentation quality mindset.
🎁 Benefits of Joining eClinical Solutions
- 💼 Work on advanced clinical data platforms
- 🌐 Exposure to global TMF & regulatory systems
- 📚 Training & mentorship with growth roadmap
- 💡 Collaborative & innovation-driven teams
📌 Note Before You Apply:
Please ensure your resume reflects TMF or document control experience. Include knowledge of eTMF systems in your CV.
👇 Application Link Will Be Visible in 15 Seconds 👇
🟢 Verified Job via Medical Jobs India – hitechplus.in
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