Pharmacovigilance & Clinical Data Management Openings at Alvotech

Alvotech, a globally recognized biopharmaceutical company specializing in biosimilars development and manufacturing, is actively hiring for multiple Pharmacovigilance (PV) and Clinical Data Management roles in Bangalore (partially remote).

This hiring initiative is part of Alvotech’s Integrated Clinical and Medical Research (iCMR) expansion, focusing on safety data management, benefit-risk evaluation, and clinical data lifecycle operations.

If you’re targeting a career in pharmacovigilance, drug safety, or clinical data management, this is a high-value opportunity in a global R&D environment.

📌 Open Positions

• Pharmacovigilance Associate (2+ years)
• Pharmacovigilance Specialist (3+ years)
• Senior Pharmacovigilance Specialist (5+ years)
• Pharmacovigilance Manager – Benefit Risk (7+ years)
• Clinical Data Management Specialist (7+ years)

🔬 Key Responsibilities

Pharmacovigilance Roles

• Perform ICSR & SAE case processing and regulatory submissions
• Conduct literature monitoring and signal detection
• Manage EudraVigilance (EV), XEVMPD, and reconciliations
• Support post-marketing surveillance and clinical trial safety
• Ensure compliance with ICH, GVP, FDA, EMA guidelines
• Work on PV system lifecycle (Argus, ARISg, Veeva Safety Vault)
• Participate in audits, inspections, and regulatory submissions
• Deliver training on pharmacovigilance processes

Clinical Data Management Role

• Manage end-to-end clinical data lifecycle (study setup → DB lock)
• Design eCRF and configure EDC systems
• Perform data validation, reconciliation, and query management
• Ensure compliance with GCP, GCDMP, 21 CFR Part 11
• Work with CDISC standards (CDASH, SDTM)
• Support eTMF documentation and audit readiness

🎓 Qualifications

• Master’s Degree in:
  • Pharmacy (M.Pharm / PharmD)
  • Life Sciences / Biotechnology / Clinical Research
  • Medicine or related fields

💼 Experience Required

🧠 Required Skills

• Strong expertise in:
  • ICSR processing, SAE handling
  • Safety databases (Argus, ARISg, Veeva Vault)
  • Clinical trial safety & post-marketing PV
  • Global regulatory frameworks (ICH, GVP, CIOMS, FDA)
• Knowledge of:
  • Biologics & biosimilars (preferred)
  • Signal detection & benefit-risk assessment
  • EDC systems (Medidata Rave, Veeva EDC, Viedoc)
• Soft skills:
  • Cross-functional collaboration
  • Time management & independent execution
  • Strong communication in global teams

💰 Salary (Estimated Market Range – India)

• PV Associate: ₹5 – ₹8 LPA
• PV Specialist: ₹8 – ₹14 LPA
• Senior PV Specialist: ₹14 – ₹22 LPA
• PV Manager: ₹22 – ₹35 LPA
• Clinical Data Manager: ₹18 – ₹30 LPA

(Based on industry benchmarks for Bangalore PV/CDM roles)

🌍 Work Model & Benefits

• Partially Remote (Hybrid flexibility)
• Exposure to global clinical trials & biosimilars portfolio
• Work in international regulatory environment
• Opportunity to work with advanced PV systems & AI-driven workflows
• Career growth in global drug safety & data science ecosystem

🚀 Why This Opportunity is High-Value

• Direct exposure to global pharmacovigilance operations
• Work on biosimilars (high-demand regulatory segment)
• Hands-on experience with Argus, Veeva Vault, EV systems
• Strong career pathway toward:
  • PV Scientist
  • Drug Safety Lead
  • Signal Management Expert
  • Benefit-Risk Specialist

📥 How to Apply

Application Link for Pharmacovigilance Associate (2+ years)

Application Link for Pharmacovigilance Specialist (3+ years)

Application Link for Senior Pharmacovigilance Specialist (5+ years)

Application Link for Pharmacovigilance Manager – Benefit Risk (7+ years)

Application Link for Clinical Data Management Specialist (7+ years)