Thermo Fisher Scientific, a global leader in clinical research and life sciences, is hiring Clinical Data Management professionals for its FSP (Functional Service Provider) model in India. These remote roles, with a hiring office in Bengaluru, offer an excellent opportunity to work on global clinical trials with top biopharmaceutical sponsors.
Currently, three positions are open:
- Clinical Data Associate I (CDA I)
- Clinical Data Associate II (CDA II)
- Clinical Coding Specialist
These roles are ideal for professionals with experience in RAVE/Veeva EDC, clinical data cleaning, reconciliation, and medical coding.
🧪 Open Positions & Responsibilities
1️⃣ Clinical Data Associate I (CDA I)
Experience: 1 – 1.6 years
Mode: Remote
Key Responsibilities:
- Perform entry-level clinical data cleaning and reconciliation
- Identify, generate, and resolve data queries
- Update clinical databases as per SOPs and GCP
- Support CRF design activities
- Collaborate with cross-functional study teams
2️⃣ Clinical Data Associate II (CDA II)
Experience: 1.6 – 3 years
Mode: Remote
Key Responsibilities:
- Lead advanced data review and cleaning activities
- Manage complex data queries and discrepancies
- Perform SAE and third-party vendor reconciliations
- Review data listings and validation reports
- Prepare CDM status reports for clients and stakeholders
3️⃣ Clinical Coding Specialist
Experience: 1 – 1.6 years
Mode: Remote
Key Responsibilities:
- Code medical and clinical terminology using MedDRA & WHO-DD
- Review coding listings as per Coding Plan and DVM
- Resolve coding-related data issues with sites and teams
- Maintain inspection-ready coding documentation
- Provide coding guidance to CDM project teams
🎓 Qualifications & Skills (All Roles)
Educational Requirement:
- Bachelor’s degree or equivalent in Life Sciences, Pharmacy, or related field
Technical Skills:
- Hands-on experience with RAVE / Veeva EDC
- Knowledge of GCP, SOPs, Data Validation Manuals
- (For Coding Specialist) Experience with MedDRA & WHO-DD
Core Competencies:
- Strong attention to detail and analytical skills
- Excellent written and verbal communication
- Ability to work independently and in global teams
- High standards of confidentiality and data integrity
💼 Benefits & Career Growth
- 🌍 Work on international clinical trials across multiple phases
- 🏠 Remote work with India-based global teams
- 📈 Clear career progression (Senior CDM, CDTL, CDM PM, Data Standards)
- 🧠 Continuous learning, mentorship & AI-enabled CDM tools
- 🏢 Opportunity to work with a top global biopharmaceutical sponsor
📝 How to Apply
Application Link for Clinical Data Associate I (CDA I)
Application Link for Clinical Data Associate II (CDA II)
Application Link for Clinical Coding Specialist
