Are you looking to elevate your career in Clinical Research? A major global Clinical Research Organization, Fortrea, is currently hiring for the position of TMF Classifier II in Bangalore. This is a fantastic opportunity for professionals with experience in eTMF management and a strong understanding of GCP/ICH guidelines to join a dynamic team in a hybrid work environment. 🚀
📌 Job Overview & Primary Role
The TMF Classifier II plays a critical role in maintaining the integrity of the Trial Master File (TMF). You will be responsible for document classification under Smart Inbox and performing Audit Ready Checks (ARC) to ensure every document is accurate, readable, and compliant. This role is essential for keeping clinical studies in a constant state of audit readiness. 📁✅
🧩 Key Responsibilities
- eTMF Management: Handle Trial, Country, and Site artifacts in accordance with established TMF processes.
- Quality Control: Perform visual quality checks on e-documents to confirm image clarity and readability before release. 🧐
- Audit Readiness: Conduct Audit Ready Checks (ARC) to ensure compliance with SOPs, GCP, and ICH guidelines.
- Issue Resolution: Identify operational issues and implement corrective actions.
- Collaboration: Work with global teams and participate in audits. 🤝
- Continuous Improvement: Contribute to quality and productivity initiatives.
📝 How to Apply
Interested candidates can apply directly through the official job portal using the link below:
📌 Pro Tip: Before applying, ensure your CV highlights:
- Experience with eTMF systems
- Familiarity with Smart Inbox workflows
- Knowledge of GCP/ICH guidelines
🎓 Required Qualifications & Experience
- Education: Bachelor’s Degree in Life Sciences or related field (Master’s preferred). 🎓
- Experience: 1–2 years in a clinical research environment.
- Technical Skills: Microsoft Office, Adobe Acrobat, and clinical systems.
- Compliance Knowledge: Strong understanding of regulatory documentation standards.
- Soft Skills: Communication, teamwork, and mentoring ability. 🌟
📍 Work Environment & Logistics
- Location: Bangalore (Hybrid Model)
- Job Type: Full-time
- Deadline: April 10, 2026 ⏳ (Only 1 day left!)
- Requisition ID: 261558
💡 Why Apply?
This role offers a perfect blend of technical document management and strategic clinical operations. If you are detail-oriented and passionate about compliance in the pharmaceutical industry, this is a great opportunity to grow your career. 💼✨
