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Navitas Life Sciences Hiring Clinical Trials – ICSR
Navitas Life Sciences
M.Pharm/B.Pharm Clinical Trials & ICSR Vacancy | Bangalore
Hiring experienced Pharmacovigilance & Clinical Trials professionals (7–10 yrs) at Navitas Life Sciences, Bangalore. Apply now – Hybrid/WFO roles.
At Navitas Life Sciences, we’re inviting passionate, experienced professionals to join our Clinical Trials and ICSR (Individual Case Safety Report) operations team in Bangalore (Whitefield). If you have strong expertise in pharmacovigilance, clinical trial operations, and safety reporting, this is your opportunity to work with one of the most reputed global life sciences organizations driving healthcare innovation.
Company Overview
Navitas Life Sciences, a part of TAKE Solutions, is a globally trusted partner in clinical research, regulatory compliance, and pharmacovigilance operations. With decades of experience serving leading pharmaceutical and biotechnology companies, Navitas is known for its deep domain expertise, data-driven insights, and commitment to improving patient safety worldwide.
Our collaborative, technology-driven environment empowers professionals to deliver excellence in clinical and post-marketing safety monitoring. By joining Navitas, you become part of a global team that values scientific rigor, continuous learning, and ethical responsibility.
Job Role & Responsibilities
The Clinical Trials – ICSR Specialist role involves overseeing pharmacovigilance and safety operations across clinical trial and post-marketing projects. The position requires analytical thinking, regulatory knowledge, and precision in managing case reports and submissions.
Key Responsibilities:
- Perform case processing, review, and submission of ICSRs (Individual Case Safety Reports) as per global regulatory timelines.
- Oversee the conduct of clinical trials and ensure compliance with GCP, PV regulations, and SOPs.
- Manage post-marketing surveillance activities to assess drug safety and efficacy.
- Provide operational oversight on assigned projects ensuring timely delivery and quality standards.
- Collaborate with cross-functional teams including clinical operations, regulatory affairs, and safety science.
- Support audit readiness and documentation for regulatory inspections.
- Contribute to process improvement initiatives and knowledge sharing within the PV department.
Eligibility / Qualifications
Education:
- M.Pharm, B.Pharm, or Pharm.D (Doctor of Pharmacy)
Experience:
- 7 to 10 years of hands-on experience in Pharmacovigilance, Clinical Trials, and Safety Data Management.
- Strong understanding of ICSR regulations, global PV processes, and clinical research workflows.
Desired Skills:
- Proficiency in safety databases (Argus/ARISg or equivalent)
- Knowledge of MedDRA, WHO-DD, and EudraVigilance
- Familiarity with signal detection, aggregate reporting, and compliance monitoring
- Excellent communication, analytical, and team coordination skills
Location & Work Mode
Location: Whitefield, Bangalore
Work Mode: Hybrid / Work From Office (WFO)
Navitas Life Sciences promotes work-life balance through flexible work models while maintaining the highest industry standards in quality and compliance.
Salary & Benefits
- Competitive industry salary package based on experience and qualifications
- Performance-based incentives and annual appraisals
- Comprehensive health and life insurance benefits
- Learning and development opportunities
- Global exposure and collaborative work culture
Application Process
Interested candidates with relevant experience can apply by sending their updated CVs to careers@navitaslifesciences.com with the subject line “Application for Clinical Trials – ICSR Specialist, Bangalore”.
Apply before October 20, 2025, to secure your spot in this exciting opportunity!
Why Join Navitas Life Sciences?
- Work with a global leader in Pharmacovigilance and Clinical Research.
- Be part of a collaborative, innovation-driven team that values professional growth.
- Gain access to world-class infrastructure and cutting-edge technology.
- Make a real impact on patient safety and public health through data-driven science.
Frequently Asked Questions (FAQs)
1. Who can apply for this role?
Candidates with 7–10 years of experience in clinical trials, ICSR processing, or pharmacovigilance can apply. Educational background in M.Pharm, B.Pharm, or Pharm.D is required.
2. Is this a remote position?
Navitas offers Hybrid flexibility; however, candidates should be open to working from the Bangalore office when required.
3. What is the selection process?
Shortlisted candidates will go through technical evaluation, HR interview, and final discussion with department heads.
4. Are freshers eligible to apply?
No, this role is designed for professionals with relevant industry experience.
5. What are the working hours?
Standard 9-hour shifts with flexible timings depending on project requirements.
Summary Table
| Category | Details |
|---|---|
| Company | Navitas Life Sciences |
| Vacancies | Clinical Trials – ICSR (1 Opening) |
| Required Education | M.Pharm, B.Pharm, Pharm.D |
| Experience | 7–10 Years |
| Location | Whitefield, Bangalore |
| Work Mode | Hybrid / WFO |
| Email to Apply | careers@navitaslifesciences.com |
To apply for this job email your details to careers@navitaslifesciences.com