Clinical Trial - ICSR (Navitas)



πŸ’Š Navitas Life Sciences Hiring: Clinical Trial – ICSR Professional | Bangalore (Hybrid)

If you’re an experienced pharmacovigilance or clinical research professional looking to grow your career in a globally recognized organization, here’s an exciting opportunity you don’t want to miss.

Navitas Life Sciences — a trusted name in clinical research and drug safety — is hiring for a Clinical Trial – ICSR position at its Whitefield, Bangalore location. This role offers a chance to work with a leading team driving innovation, quality, and patient safety in global healthcare.


🌟 About Navitas Life Sciences

Navitas Life Sciences, part of the Take Solutions group, is a global Clinical Research Organization (CRO) that provides end-to-end services in clinical development, data management, pharmacovigilance, and regulatory compliance.

With more than two decades of experience, Navitas partners with top pharmaceutical and biotechnology companies worldwide, helping accelerate the development of safe and effective therapies.

The company is known for its strong scientific expertise, innovative technology platforms, and commitment to operational excellence.


🧠 Role Overview: Clinical Trial – ICSR Professional

πŸ“ Location: Bangalore (Whitefield)
πŸ’Ό Work Mode: Hybrid / Work From Office
🧾 Experience: 7–10 years
πŸŽ“ Education: M.Pharm, B.Pharm, Pharm.D

Navitas Life Sciences is looking for a skilled and motivated Clinical Trial – ICSR (Individual Case Safety Report) professional to join its dynamic Pharmacovigilance and Clinical Operations team.

The ideal candidate will have hands-on experience in clinical trial case processing, safety report submission, and post-marketing pharmacovigilance activities.


πŸ”¬ Key Responsibilities

  • Conduct and manage clinical trial safety cases and post-marketing adverse event reporting in compliance with regulatory standards.
  • Ensure timely submission and distribution of ICSR reports to clients, regulatory authorities, and internal stakeholders.
  • Participate in signal detection, case quality review, and risk assessment as per SOPs and global guidelines.
  • Collaborate cross-functionally with global teams to support ongoing clinical studies.
  • Provide oversight on operational projects and ensure data accuracy, compliance, and efficiency.

🎯 Candidate Profile

To succeed in this role, candidates should possess:

  • 7–10 years of experience in clinical trial operations and pharmacovigilance (ICSR case management).
  • In-depth understanding of ICH-GCP, MedDRA coding, and safety data reporting.
  • Excellent written and verbal communication skills.
  • Strong attention to detail, time management, and teamwork abilities.

🧬 Why Join Navitas Life Sciences?

Working at Navitas means being part of a culture built on collaboration, innovation, and continuous learning.

Here’s what makes this opportunity special:
✅ Exposure to global clinical studies and safety operations.
✅ Opportunity to work with world-class pharmacovigilance systems.
✅ Flexible hybrid work model.
✅ Competitive benefits and professional growth opportunities.

You’ll be joining a team that plays a crucial role in ensuring patient safety and regulatory compliance across the entire clinical development lifecycle.


πŸ“© How to Apply

If this sounds like your next career move, send your CV to:
πŸ“§ recruitment.bangalore@navitaslifesciences.com
πŸ“Œ Subject line: Clinical Trial – ICSR Role


🌍 Final Thoughts

The Clinical Trial – ICSR role at Navitas Life Sciences is an excellent opportunity for experienced professionals who want to make an impact in global drug safety and clinical research.

By joining Navitas, you’ll contribute to improving patient outcomes while advancing your career in one of the most respected life-sciences organizations.

Apply today and become part of a team that’s shaping the future of clinical research.


πŸ’¬ Not a recruiter — just resharing this excellent opportunity for professionals in the pharmacovigilance and clinical research field.


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