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TransPerfect Hiring Clinical Document Specialist (TMF) – Freshers
TransPerfect
Pune
0–1 Years
Clinical Research
TMF / eTMF
Life Sciences
🏢 About TransPerfect
TransPerfect is a global provider of language and technology solutions supporting pharmaceutical, biotechnology, and clinical research organizations worldwide. The company plays a major role in clinical trial documentation, regulatory compliance, and global research support services.
📌 Job Overview
- Role: Clinical Document Specialist I
- Location: Pune, Maharashtra
- Experience: 0–1 Year
- Industry: Clinical Research / Life Sciences / CRO
- Employment Type: Full-Time, Permanent
- Work Mode: On-site
🔬 Key Responsibilities
- Review essential and non-essential Trial Master File (TMF) documents
- Index and accurately file documents in eTMF systems
- Ensure documentation meets regulatory standards and SOP requirements
- Maintain quality thresholds and productivity targets
- Update study trackers and documentation for project managers
- Coordinate with Clinical Document Team Leads on project queries
- Support User Acceptance Testing (UAT) during system updates
- Identify workflow challenges and recommend improvements
- Communicate effectively with internal teams and stakeholders
🎓 Eligibility Criteria
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field
- 0–1 year of experience in Life Sciences industry
- Knowledge of clinical trial phases and development processes
- Understanding of ICH-GCP guidelines
- Familiarity with clinical study documents and TMF structure
- Proficiency in Microsoft Office (Word, Excel, Outlook)
- Knowledge of eClinical or eTMF systems is an advantage
- Strong attention to detail and documentation skills
⭐ Career Growth Opportunities
- Exposure to global clinical trial documentation standards
- Hands-on experience with eTMF and eClinical systems
- Opportunity to work with global clinical research teams
- Career growth into roles like:
- TMF Specialist
- Clinical Trial Associate (CTA)
- Clinical Data Specialist
- Clinical Project Coordinator
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Understanding TMF structure, clinical documentation standards, and ICH-GCP guidelines will increase your chances of being shortlisted.
Kindly read the entire job description carefully before applying. Understanding TMF structure, clinical documentation standards, and ICH-GCP guidelines will increase your chances of being shortlisted.
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