Urgent hiring: Senior/Lead Medical Reviewer with 1–3+ years in Aggregate Reporting/Signal Management/RMP. Join Navitas Life Sciences in Bangalore for exciting pharmacovigilance jobs and drug safety careers in India. Full-time opportunity in a growing global team!
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About the Company
Navitas Life Sciences, a TAKE Solutions Enterprise, is a globally recognized full-service CRO and clinical research consultancy delivering end-to-end drug development, regulatory, and pharmacovigilance services.
With over 30 years of expertise, Navitas supports top pharmaceutical, biotech, and medical device companies through innovative technology-driven solutions, real-world evidence, and patient-centric approaches.
The company operates across North America, Europe, and Asia-Pacific with a strong presence in India. Headquartered in Princeton (USA) and Chennai (India), Navitas Life Sciences is known for regulatory compliance, scientific excellence, and operational efficiency.
Its pharmacovigilance division provides comprehensive safety writing, signal detection, risk management, and aggregate reporting services that meet global regulatory standards (ICH, GVP, FDA, EMA).
Job Details
- Company Name: Navitas Life Sciences
- Experience: Minimum 1–3+ years in Aggregate Reporting, Signal Management, or Risk Management Plans
- Qualification: Graduate/Post-Graduate in Life Sciences, Pharmacy, Medicine, Dentistry, Allied Health Sciences or related fields
- Location: Bangalore (Bengaluru), Karnataka, India
- Work Type: On-site / Hybrid (Full-time)
Job Description
Navitas Life Sciences is expanding its Pharmacovigilance & Safety team in Bangalore and urgently requires experienced Senior/Lead Medical Reviewers. This pivotal role focuses on medical oversight of aggregate safety reports and risk management documents.
You will lead safety writing activities, mentor junior team members, ensure medical cohesiveness, and act as the primary medical contact for clients and health authorities.
Senior/Lead Medical Reviewer
- Department: Pharmacovigilance and Safety (Aggregate Reporting Team)
- Role: Senior/Lead Medical Reviewer (Associate level)
- Experience: 1–3+ years in Aggregate Reporting / Signal Management / RMP
- Education/Qualification: Graduate or Post-Graduate in Life Sciences, Pharmacy, Medicine, Dentistry, or Allied Health Sciences
Skills/Qualifications
- Strong medical & pharmacovigilance terminology knowledge
- In-depth understanding of GCP, GVP, ICH, USFDA, EMA guidelines
- Proficiency in aggregate reports (PSUR, PBRER, DSUR, PADER, RMP, Canadian AR)
- Excellent written & spoken English (additional languages a plus)
- Advanced MS Office skills (Word, Excel, PowerPoint)
- Leadership, mentoring & project management abilities
- Strong communication, organization & team collaboration skills
- Experience in client interaction & regulatory audits/inspections
Key Responsibilities
- Provide medical review of RMPs, PSURs, PBRERs, DSURs, PADERs
- Ensure medical cohesiveness and scientific accuracy
- Mentor team members for independent high-quality delivery
- Oversee timelines, budget, and quality of safety reports
- Act as primary medical contact for clients
- Coordinate with cross-functional authors globally
- Lead internal/external audits and inspections
- Author/review aggregate reports and annexes
- Develop project-specific training and guidance documents
- Support ICSRs and literature review teams when required
- Maintain trackers and ensure procedural compliance
- Conduct daily status meetings and training sessions
Benefits/Perks
- Competitive salary with performance incentives
- Comprehensive health insurance and wellness programs
- Rapid career progression in global pharmacovigilance
- Continuous training and certification support
- Exposure to international clients and regulatory submissions
- Collaborative, learning-oriented culture
- Flexible/hybrid work options (Bangalore)
- Opportunity to lead high-impact safety projects
How to Apply
Interested candidates should apply through the official Navitas Life Sciences career portal at https://navitaslifesciences.com/careers or send updated resumes mentioning “Senior/Lead Medical Reviewer – Bangalore” in the subject line to the HR team.
For more pharmacovigilance jobs, drug safety openings, and expert guidance in India, visit Pharma Recruiter.
Verified Post
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Don’t miss this chance to advance your drug safety career with a leading global CRO – apply today!
Why You Should Join
Navitas Life Sciences offers a stimulating environment where medical and scientific expertise directly contributes to patient safety worldwide. With a strong focus on innovation, compliance, and professional development, employees enjoy long-term stability and global exposure.
The Bangalore center is a hub for pharmacovigilance excellence, providing opportunities to work on cutting-edge aggregate reporting and risk management projects for top-20 pharma clients.
Join a company recognized for quality, integrity, and employee growth in one of the fastest-growing pharmacovigilance teams in India.
FAQs
1–3+ years specifically in Aggregate Reporting, Signal Management, or Risk Management Plans (RMP) with strong medical reviewing background.
Yes, medical graduates (MBBS, MD, BDS, PharmD) and post-graduates in life sciences/pharmacy are highly preferred.
RMP, PSUR, PBRER, DSUR, PADER, Canadian Summary Reports, and related annexes with full medical oversight.
Fast-track leadership roles, global client exposure, continuous regulatory training, and progression to Principal Medical Reviewer or Safety Management positions.
