Navitas Life Sciences is hiring freshers for Trainee Drug Safety Associate roles in Bangalore. Apply by June 30, 2025. Start your pharmacovigilance career with global clients in a USFDA-compliant CRO. Great opportunity for B.Pharm, M.Pharm, Pharm.D, and Life Sciences graduates.
Navitas Life Sciences Hiring Freshers – Trainee Drug Safety Associate Jobs in Bangalore 2025
Are you a fresh pharmacy or life sciences graduate seeking a breakthrough in the pharmaceutical industry? Navitas Life Sciences, a global contract research organization (CRO), is inviting applications from freshers for Trainee – Drug Safety Associate roles at its Bangalore office.
This is a golden opportunity to start your career in pharmacovigilance (PV)—one of the most in-demand and high-paying sectors in the pharmaceutical industry. If you’re passionate about patient safety, drug regulation, and clinical research, this role is for you.
🧬 About Navitas Life Sciences
Navitas Life Sciences, a part of TAKE Solutions since 2005, offers end-to-end clinical research, regulatory compliance, and pharmacovigilance services to global pharmaceutical and biotechnology clients. With operational bases in Bangalore and Princeton (USA), the company supports drug safety monitoring for over 200 global products.
As a USFDA-compliant CRO, Navitas is known for its global pharmacovigilance expertise, use of industry-standard safety databases like Argus, and high standards of ICH, EMA, and MHRA compliance.
🔗 Learn more at: Navitas Career Opportunities
👩🔬 Position Overview – Trainee Drug Safety Associate
| Details | Information |
|---|---|
| Position | Trainee – Drug Safety Associate |
| Experience | Freshers (Immediate Joiners Preferred) |
| Location | Bangalore, Karnataka (Work From Office) |
| Qualification | B.Pharm, M.Pharm, Pharm.D, B.Sc./M.Sc. (Biotech, Microbiology, Biochemistry) |
| Vacancies | Not specified |
📌 Key Responsibilities
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Process Individual Case Safety Reports (ICSRs) from spontaneous sources, clinical trials, and literature.
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Conduct medical coding using MedDRA and WHO-Drug dictionaries.
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Write clear and compliant narratives for adverse drug reaction (ADR) cases.
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Perform initial triage, duplicate checks, and database entry for ICSRs.
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Maintain compliance with global PV regulations including USFDA, EMA, ICH-GCP.
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Collaborate with experienced PV professionals for quality case processing and regulatory reporting.
🎓 Required Qualifications & Skills
| Requirement | Details |
|---|---|
| Education | B.Pharm, M.Pharm, Pharm.D, B.Sc./M.Sc. (Biotech, Life Sciences) |
| Experience | Freshers welcome; internships or PV academic projects preferred |
| Technical Skills | Basic knowledge of pharmacovigilance, ICSR lifecycle, MedDRA coding, and WHO Drug Dictionary |
| Soft Skills | Strong written and verbal communication, attention to detail, analytical thinking, and teamwork |
🌟 Why Join Navitas Life Sciences?
Navitas offers a career foundation that is rare for freshers, especially in a regulated drug safety role. Here’s what sets this opportunity apart:
✅ Career Development
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Structured pharmacovigilance training program
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Hands-on experience in ICSR processing, regulatory compliance, and safety database management
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Mentorship from industry experts in global drug safety
✅ Industry Reputation
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Work with a USFDA-compliant CRO with over 200+ product safety programs
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Exposure to clients in North America, Europe, and Asia-Pacific
✅ Work Culture
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Rated 3.7/5 for learning and development on Glassdoor
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Friendly, diverse, and inclusive work environment
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Access to internal certification programs and workshops
💰 Salary & Benefits
| Benefit | Details |
|---|---|
| Salary Range | ₹2.5 – ₹3.5 LPA (Based on skill & interview performance) |
| Work Mode | Onsite (Work From Office) at Bangalore location |
| Software Exposure | Training on Argus Safety, MedDRA, and proprietary databases |
| Additional Benefits | Health insurance, team events, mentoring programs |
📩 How to Apply
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Send your resume to: roshini.m@navitaslifesciences.com
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Subject line: “Trainee Drug Safety Associate – Bangalore”
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Application deadline: June 30, 2025
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Note: Mention “Immediate Joiner” in your email if applicable.
✅ Highlight your PV-related coursework, projects, or internships in your resume.
✍️ Application Tips for Freshers
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Emphasize ICSR processing knowledge (even academic or simulated cases)
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List tools like MedDRA, WHO Drug Dictionary, or any exposure to Argus Safety Database
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Include keywords like GVP guidelines, signal detection, and case triaging if applicable
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Keep the resume clean, formatted, and tailored to pharmacovigilance.
🧭 Work Environment – Bangalore
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Office located in ITPL or Electronic City, Bangalore
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Fully onsite model with access to clinical systems
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Collaborative teams of PV scientists and drug safety professionals
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Comfortable workspace with modern IT infrastructure.
🌐 Why Pharmacovigilance is a Smart Career Choice
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Global demand for PV professionals is growing due to regulatory focus on patient safety
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India has become a hub for drug safety outsourcing, offering CRO jobs with international exposure
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Freshers with the right training can quickly scale into roles like Drug Safety Associate, Signal Analyst, or Regulatory PV Specialist
🎯 Take the Next Step Toward a Rewarding PV Career
Join Navitas Life Sciences and contribute to global drug safety and patient well-being. As a Trainee Drug Safety Associate, you’ll get world-class training, mentorship, and exposure to real-world pharmacovigilance systems.
📅 Apply by June 30, 2025, and launch your pharmacovigilance career with one of the best CROs in India!
