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Hiring Statistical Programmer, PV, TMF & Clinical Documentation Roles
Novotech
Bangalore
0–5 Years
PV / SAS / TMF
🏢 About Company
Novotech is a global CRO focused on clinical research, pharmacovigilance, and statistical programming. It offers strong exposure to global trials, regulatory systems, and data-driven healthcare roles.
1️⃣ Statistical Programmer II
- Experience: 2–5 Years
- Qualification: Biostatistics / Statistics / Life Sciences
- Responsibilities:
- SAS programming (ADaM, TLFs)
- Clinical datasets & validation
- Biostatistics collaboration
- Skills: SAS, CDISC, SQL
2️⃣ Document Management Associate (DMA)
- Experience: 0–2 Years (Freshers Eligible)
- Qualification: B.Pharm / Life Sciences
- Responsibilities:
- eTMF management
- Document QC & tracking
- SOP compliance
- Skills: TMF, GCP
3️⃣ Pharmacovigilance Associate
- Experience: 1–3 Years
- Qualification: B.Pharm / M.Pharm
- Responsibilities:
- ICSR processing
- MedDRA coding
- Safety reporting
- Skills: PV, ICSR
4️⃣ Clinical Document Specialist
- Experience: 1–3 Years
- Responsibilities:
- TMF documentation
- Audit readiness
- Tracking & QC
- Skills: TMF, documentation
5️⃣ Senior Document Management Associate
- Experience: 3–5 Years
- Responsibilities:
- TMF QC & compliance
- Multi-project handling
- Skills: Advanced TMF
🎯 Interview Preparation Tips
- Revise ICH-GCP & clinical trial lifecycle
- Understand TMF structure
- Prepare ICSR & MedDRA basics
- Learn SAS basics (PROC, DATA step)
- Prepare real examples
Helpful Resources:
📌 Note Before You Apply:
Select the role carefully based on your experience before applying.
Select the role carefully based on your experience before applying.
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