Navitas Life Sciences hiring for regulatory affairs, pharmacovigilance, clinical research, clinical data management, SAS programming jobs. Apply globally with top pharma salaries.
Navitas Life Sciences Global Hiring 2025: High Salary Pharma Jobs for Regulatory Affairs, Pharmacovigilance, Clinical Research, CDM & SAS Programming
The global pharmaceutical industry continues to boom in 2025, and Navitas Life Sciences stands as a global leader in driving innovation across regulatory affairs, pharmacovigilance, clinical research, data management, and biostatistics. If you’re a life sciences professional seeking a high-paying pharma career with international exposure, Navitas Life Sciences is actively hiring both freshers and experienced professionals across India and globally.
With multiple open positions in Chennai and Bangalore, this is your chance to build a dynamic career with one of the fastest-growing global life sciences organizations.
🌍 About Navitas Life Sciences
Navitas Life Sciences is a globally trusted partner for leading pharmaceutical, biotechnology, and medical device companies. With end-to-end solutions across clinical development, regulatory affairs, pharmacovigilance, real-world evidence, and data sciences, Navitas empowers organizations to bring innovative therapies to market faster and more safely.
🌟 Why Navitas Life Sciences?
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Global client portfolio including leading pharma companies across the USA, Europe, Canada, and Asia.
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Expertise in navigating complex regulatory landscapes with full USFDA, EMA, Health Canada, PMDA, and MHRA compliance.
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Cutting-edge technology platforms for data management, eCTD submissions, safety reporting, and SAS programming.
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Continuous career advancement opportunities in clinical research, regulatory, and safety domains.
🔎 Who Should Apply?
Navitas is actively seeking talented candidates from:
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Life Sciences (B.Pharm, M.Pharm, MBBS, MD, MSc, PhD)
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Medical Graduates (Physicians, Pharmacologists, Biostatisticians)
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SAS Programmers & Data Scientists
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Clinical Data Managers
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Regulatory Affairs Specialists
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Pharmacovigilance Experts
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Biostatisticians & Statistical Programmers
Whether you’re an experienced expert or a fresher looking to start your journey, Navitas offers high-growth opportunities in India’s most lucrative pharmaceutical sector.
🔥 Current Openings at Navitas Life Sciences
1️⃣ Junior Regulatory Associate
- Location: Chennai, India
- Job Type: Full-Time
- Experience Level: Entry-Level
- Qualification: Bachelor’s Degree in Pharmacy
Key Responsibilities:
- Assist in regulatory submissions for IND, ANDA, NDA, DMF.
- Work with global regulatory agencies: USFDA, EMA, Health Canada, MHRA.
- Support electronic document publishing (eCTD submissions), hyperlinking, bookmarking, TOC creation.
- Manage document-level publishing and submissions per organizational SOPs.
Required Skills:
- Knowledge of global regulatory frameworks.
- Strong organizational, publishing, and submission archiving skills.
- Attention to detail for compliance and data integrity.
2️⃣ Regulatory Associate – Trainee
- Location: Chennai, India
- Job Type: Full-Time
- Qualification: Bachelor’s Degree in Pharma
Key Responsibilities:
- Support in preparing regulatory dossiers in CTD/eCTD formats.
- Document-level publishing, submission support, and archiving.
- Work closely with cross-functional regulatory and QA teams.
Desired Skills:
- Knowledge of global eCTD standards.
- Familiarity with ICH, GCP, GMP, and regulatory submissions.
- Detail-oriented with strong publishing software expertise.
3️⃣ Safety Specialist II (Pharmacovigilance)
- Location: Bangalore, India
- Job Type: Full-Time
- Qualification: Life Sciences/Pharma/Medical Graduate/Postgraduate
Key Responsibilities:
- Author & review safety aggregate reports: DSUR, PBRER, PSUR.
- Signal detection and risk management planning.
- Perform medical literature surveillance for safety signals.
- Ensure full compliance with GVP Module VII, ICH E2E, and USFDA pharmacovigilance guidelines.
Desired Skills:
- Deep understanding of pharmacovigilance regulations.
- Aggregate reporting expertise.
- Signal management experience.
- Excellent medical writing and data analysis skills.
4️⃣ Principal SAS Programmer
- Location: Bangalore, India
- Job Type: Full-Time
- Qualification: Life Sciences Graduate/Postgraduate
Key Responsibilities:
- Lead SAS programming deliverables for global clinical trials.
- Generate SDTM, ADaM datasets per CDISC standards.
- Deliver TLFs (Tables, Listings, Figures) for regulatory submissions.
- Handle client interactions, troubleshooting, and resource planning.
Desired Skills:
- Expert in SAS programming.
- Proficient in CDISC SDTM/ADaM standards.
- Clinical trial data programming expertise.
- Leadership and people management capabilities.
5️⃣ Clinical Data Analyst
- Locations: Chennai & Bangalore, India
- Job Type: Full-Time
- Qualification: Life Sciences or Engineering Graduate
Key Responsibilities:
- Develop and validate SAS programs for efficacy & safety data analysis.
- Prepare clinical study reports (CSRs), data listings, tables, and figures.
- Manage multiple projects, ensuring strict regulatory compliance.
Desired Skills:
- 2.5 to 3 years of clinical data analysis experience.
- Proficiency in SAS programming.
- SAS certification preferred.
- Understanding of clinical development phases.
🌟 Global Exposure with Navitas Life Sciences
At Navitas, you’ll work on global clinical research and regulatory projects for clients across:
- United States (USFDA)
- Europe (EMA)
- Canada (Health Canada)
- Japan (PMDA)
- Australia (TGA)
- India (DCGI, CDSCO)
This means international exposure, fast career growth, and high salary potential with lucrative pharmaceutical regulatory compliance jobs.
💼 Why Choose Navitas Life Sciences?
✅ High Salary Packages: Competitive pay with international pharma standards.
✅ Global Regulatory Exposure: Work with top-tier global regulatory authorities.
✅ Rapid Career Growth: Opportunities for promotions, certifications, and leadership roles.
✅ Innovative Technologies: Hands-on experience with eCTD publishing, SAS programming, advanced pharmacovigilance tools.
✅ Collaborative Work Culture: Inclusive, diverse, and learning-oriented environment.
✅ Work-Life Balance: Flexible work hours, remote work options, and a supportive team.
📧 How to Apply for Navitas Life Sciences Careers
If you are passionate about building your career with a global pharma leader, apply now:
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🔗 Global Application Portal: Navitas Careers Page
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📩 Location-wise Direct Email Submissions:
Website: www.navitaslifesciences.com
