Thermo Fisher Scientific has announced 7 major hiring opportunities in India across Clinical Data Management (CDM), Pharmacovigilance (PV), Safety Writing, Bioinformatics, and Project Management domains. These roles are open for experienced professionals seeking remote and Bangalore-based pharma and biotech careers.
This is a high-impact opportunity for candidates in drug safety, clinical research, regulatory writing, bioinformatics, and data management to work with one of the world’s leading life sciences organizations.
📌 Open Positions
- CDM Programmer II (Veeva Vault EDC) – Fully Remote
- Safety Writer II – Remote India
- Safety Writer III – Remote India
- Safety Writer IV – Remote India
- Manager, PV – Safety Writing – Remote India
- Business Analyst III – Bangalore (Hybrid)
- Project Coordinator – Bangalore (Hybrid)
🔬 Role-Wise Details
1️⃣ CDM Programmer II (Veeva Vault EDC)
Key Responsibilities:
- Database development & edit checks in Veeva Vault EDC
- Retrospective Amendment management
- Data validation programming
- SAS, SQL, Rave system handling
- Clinical database listings and data review
Qualifications:
- Bachelor’s degree
- 4+ years in Clinical Data Management programming
- Strong knowledge of GCP and SOP compliance
Salary (Estimated):
₹10 – ₹18 LPA
2️⃣ Safety Writer II
Key Responsibilities:
- Authoring DSURs, PSURs, PBRERs, PA(D)ERs
- Data review & quality control
- Regulatory aggregate reporting
- Project management of safety deliverables
Qualifications:
- Bachelor’s or higher scientific degree
- 5+ years safety writing experience
Salary:
₹12 – ₹22 LPA
3️⃣ Safety Writer III
Key Responsibilities:
- Author & senior review of DSURs, RMPs, PBRERs
- High-complexity regulatory documents
- Client-facing responsibilities
- Mentoring junior writers
Qualifications:
- 6+ years aggregate safety reporting experience
- Expertise in ICH & US PV regulations
Salary:
₹18 – ₹28 LPA
4️⃣ Safety Writer IV
Key Responsibilities:
- Lead high-complexity RMPs & marketing authorization content
- Serve as subject matter expert
- Oversee deliverables & regulatory responses
Qualifications:
- 8+ years pharmacovigilance writing experience
- Advanced knowledge of global PV compliance
Salary:
₹25 – ₹40 LPA
5️⃣ Manager, PV – Safety Writing
Key Responsibilities:
- Manage global aggregate safety reports
- Lead RMP strategy
- Staff management & performance oversight
- Regulatory audit preparation
Qualifications:
- 5+ years safety writing
- 1+ year leadership experience
Salary:
₹30 – ₹45 LPA
6️⃣ Business Analyst III (Bioinformatics)
Key Responsibilities:
- Agile product ownership
- Bioinformatics domain testing
- AWS/Web-based scientific software validation
- CAR-T & cell/gene therapy experience
Qualifications:
- MSc/PhD in Bioinformatics/Computational Biology
- 5+ years in NGS, assay design
Salary:
₹18 – ₹30 LPA
7️⃣ Project Coordinator
Key Responsibilities:
- PMO coordination
- Agile project tracking
- Cross-functional marketing collaboration
- Risk management & workflow optimization
Qualifications:
- 3–5 years project coordination
- Agile/Scrum knowledge
Salary:
₹8 – ₹14 LPA
🌍 Why Join Thermo Fisher Scientific?
- Global exposure across 100+ countries
- Work with top 50 pharma companies
- Remote flexibility
- Strong pharmacovigilance & clinical research ecosystem
- Career growth in drug safety and regulatory writing
These roles are ideal for professionals in:
- Pharmacovigilance jobs India
- Safety writing jobs remote India
- Clinical data management jobs
- Bioinformatics pharma jobs
- PV manager jobs India
📥 How to Apply
Application Link For Project Coordinator
Application Link For CDM Programmer II (Veeva Vault EDC)
Application Link For Safety Writer II
Application Link For Safety Writer III
Application Link For Safety Writer IV
Application Link For Manager, PV – Safety Writing
Application Link For Business Analyst III
