Discover exciting pharma jobs in India with this Pharmacovigilance Associate role. Build a rewarding career in drug safety and regulatory compliance. Perfect for professionals seeking growth in pharmaceutical careers across clinical studies and post-marketing surveillance. Explore similar QA jobs, QC jobs, and production opportunities in the booming Indian pharma sector.
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About the Company
This leading organization specializes in clinical research and pharmacovigilance services, delivering high-quality drug safety solutions to global clients. With a strong focus on innovation, the company maintains strict regulatory compliance with ICH-GCP guidelines and international standards.
It fosters a culture of excellence, continuous learning, and professional development while expanding its footprint in the pharmaceutical industry. Employees benefit from a dynamic environment that supports long-term career stability and global exposure in drug safety management.
Job Details
- Company Name: Novotech (or similar leading CRO/Pharma services firm)
- Experience: Varies by role (typically 0–5 years; entry-level to mid-level opportunities available)
- Qualification: Bachelor’s or Master’s in Pharmacy (B.Pharm/M.Pharm), Life Sciences, Pharm.D, or related fields
- Location: India (multiple locations including major pharma hubs)
- Work Type: On-site / Hybrid
Job Description
The Pharmacovigilance Associate role focuses on ensuring patient safety through effective monitoring of clinical trials and marketed products. This position belongs to the Drug Safety / Pharmacovigilance department and supports both clinical development and post-marketing activities in line with global regulatory expectations.
Pharmacovigilance Associate
- Department: Pharmacovigilance / Drug Safety
- Market: India (Global client support)
- Role: Pharmacovigilance Associate
- Experience: Varies (0–5 years preferred in safety data handling)
- Education/Qualification: B.Pharm, M.Pharm, Life Sciences, or equivalent
Skills/Qualifications
- Strong knowledge of ICH-GCP guidelines and pharmacovigilance regulations
- Experience in processing Individual Case Safety Reports (ICSRs), including SAE, SUSAR, and AE
- Proficiency in safety database setup and management
- Excellent attention to detail and analytical skills for case triage and data entry
- Ability to prepare Safety Management Plans
- Good communication and teamwork abilities
- Understanding of MedDRA coding and regulatory submission timelines
- Willingness to ensure full compliance with SOPs and applicable laws
Key Responsibilities
- Monitor safety mailbox and acknowledge case receipts promptly
- Prepare Safety Management Plans for clinical studies
- Set up safety databases for new studies
- Process and submit ICSRs (SAE/SUSAR/AEs) accurately
- Ensure compliance with ICH-GCP, SOPs, and regulatory requirements
- Support post-marketing surveillance activities
- Perform case triage, data entry, and follow-up as needed
- Maintain timely reporting and documentation standards
Benefits/Perks
- Career growth opportunities in global pharmacovigilance projects
- Continuous learning through training on latest regulatory updates
- Competitive salary and performance-based incentives
- Collaborative work culture with emphasis on innovation
- Global exposure to international clinical trials and safety standards
- Supportive environment for professional development
How to Apply
Interested candidates can apply by sending their updated resume to the official HR email or through the company career portal. Mention “Pharmacovigilance Associate Application” in the subject line. For more pharma job listings and career guidance, visit Pharma Recruiter.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Novotech Career page.
Act now and take the next step in your pharmaceutical career!
Why You Should Join
Joining this role offers a chance to work in a recognized company known for its commitment to patient safety and regulatory excellence. You will thrive in a supportive culture that values innovation and teamwork while providing long-term career stability.
Gain valuable experience in cutting-edge pharmacovigilance practices, enjoy continuous learning opportunities, and contribute to global drug safety initiatives in India’s thriving pharma industry.
FAQs
What qualifications are needed for the Pharmacovigilance Associate role?
A degree in Pharmacy (B.Pharm/M.Pharm), Life Sciences, or related fields is typically required. Prior experience in drug safety is preferred but entry-level opportunities exist.
How do I apply for this pharma job in India?
Send your resume via the official career email or portal with a clear subject line. Check the company website for the latest application details.
Is experience mandatory for Pharmacovigilance Associate positions?
Experience varies; many roles welcome freshers or candidates with 0–2 years, while others seek 2–5 years in case processing or safety surveillance.
What growth opportunities exist in pharmacovigilance careers?
Professionals can advance to senior associate, team lead, or specialist roles with exposure to global projects, regulatory affairs, and higher responsibilities in drug safety.
