Elevate your pharmacovigilance career! Navitas Life Sciences hires Safety Associates for Risk Management Plans in Bangalore. 1-4 years experience in RMP drafting and PBRER review. Join India’s leading CRO now.
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About the Company
Navitas Life Sciences is a technology-driven Contract Research Organization (CRO) headquartered in Princeton, NJ, with global operations including Bangalore, India. Backed by H.I.G. Capital since 2022, it delivers end-to-end solutions in clinical development, regulatory affairs, pharmacovigilance, and data sciences to pharma and biotech clients.
With over 35 years of expertise, Navitas accelerates life-saving therapies through innovative platforms like pvnet® for safety surveillance, ensuring regulatory compliance and patient-centric outcomes across 20+ therapeutic areas.
Job Details
- Company Name: Navitas Life Sciences
- Experience: 1–4 years
- Qualification: M.Pharm, B.Pharm, Pharm.D
- Location: Bangalore, Whitefield
- Work Type: Full-time, WFO/Hybrid
Job Description
Navitas Life Sciences is hiring Safety Associates specialized in Risk Management Plans (RMP) to support pharmacovigilance operations. This role focuses on regulatory safety documentation for global pharma clients.
Safety Associate (RMP)
- Department: Pharmacovigilance / Regulatory Safety
- Role: Draft innovator RMPs, review PBRERs, and develop risk management strategies
- Experience: 1–4 years
- Education/Qualification: M.Pharm, B.Pharm, Pharm.D
Skills/Qualifications
- M.Pharm, B.Pharm, or Pharm.D from a recognized institution
- 1–4 years in pharmacovigilance with focus on RMP drafting and review
- Proficiency in developing Risk Management Plans for innovator products
- Experience in reviewing and authorizing Periodic Benefit-Risk Evaluation Reports (PBRER)
- Strong knowledge of global regulatory guidelines (ICH, FDA, EMA)
- Excellent documentation and analytical skills
Key Responsibilities
- Draft comprehensive Risk Management Plans (RMP) for innovator drugs
- Review and authorize PBRER submissions for regulatory compliance
- Develop and update risk minimization strategies and safety profiles
- Support signal detection and benefit-risk assessments
- Collaborate on regulatory filings and safety surveillance activities
- Ensure adherence to pharmacovigilance standards and timelines
Benefits/Perks
- Competitive salary with performance incentives
- Hybrid work model promoting flexibility
- Opportunities for growth in a global CRO environment
- Access to advanced PV platforms and training programs
- Comprehensive health benefits and wellness initiatives
- Contribution to life-saving therapies for global patients
How to Apply
Send your updated resume to the HR team via the Navitas careers portal or email careers@navitaslifesciences.com. Mention “Safety Associate (RMP) – Bangalore” in the subject line. Immediate joiners preferred.
Location Details
- Location: Navitas Life Sciences, Whitefield, Bangalore
- Contact/Email: careers@navitaslifesciences.com
Why You Should Join
Navitas Life Sciences offers a dynamic platform in Bangalore’s Whitefield tech hub to specialize in pharmacovigilance, supporting global drug safety with cutting-edge tools and collaborative teams.
Thrive in a patient-focused culture, accelerate career growth through regulatory expertise, and contribute to innovative therapies reaching millions. With hybrid flexibility and industry recognition, secure long-term stability in India’s booming life sciences sector. Explore more pharma job opportunities.
FAQs
Q1: What experience is required for the Safety Associate (RMP) role?
A: 1 to 4 years in pharmacovigilance, specifically in RMP drafting and PBRER review.
A: M.Pharm, B.Pharm, or Pharm.D degrees.
Q3: What work mode is available for this job in Bangalore?
A: Work From Office (WFO) or Hybrid model.
Q4: How many positions are open for Safety Associate (RMP)?
A: 24 positions available in Whitefield, Bangalore.
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