Exciting opportunity for experienced professionals! Join ProPharma as a Pharmacovigilance Scientist in India. This role focuses on aggregate safety reports, signal management, and risk management plans. Perfect for candidates seeking pharma jobs and pharmaceutical careers in India in a global PV environment.
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About the Company
ProPharma is a leading global provider of regulatory sciences, clinical, quality, and pharmacovigilance services to the pharmaceutical, biotechnology, and medical device industries. With over 25 years of expertise, the company partners with clients through an advise-build-operate model across the complete product lifecycle.
Known for deep domain knowledge, regulatory compliance, innovation, and operational excellence, ProPharma helps de-risk and accelerate high-profile drug and device programs while maintaining the highest standards of patient safety and quality.
Job Details
- Company Name: ProPharma
- Experience: Minimum 2+ years in Pharmacovigilance
- Qualification: Bachelor’s or Master’s degree in Pharmacy, Nursing, Life Sciences, or related healthcare/scientific field
- Location: India (Hyderabad preferred)
- Work Type: Remote (with periodic office attendance)
Job Description
ProPharma is actively hiring a Pharmacovigilance Scientist to join its Benefit-Risk team in India. This full-time role supports critical pharmacovigilance activities, focusing on high-quality safety documentation, regulatory compliance, and cross-functional collaboration in a dynamic global environment.
Pharmacovigilance Scientist
- Department: Pharmacovigilance / Benefit-Risk
- Market: Pharmaceutical & Biopharma
- Role: PV Safety Scientist
- Experience: 2+ years in Pharmacovigilance
- Education/Qualification: Bachelor’s/Master’s in Pharmacy, Life Sciences, Nursing or related field
Skills/Qualifications
- Strong analytical, problem-solving, and organizational skills
- Excellent attention to detail and commitment to quality
- Superior written and verbal communication, especially in medical writing
- Ability to interpret and summarize complex scientific data
- Solid understanding of global PV regulations (ICH-GCP, FDA, EMA)
- Proficiency in MS Office (Word, Excel, PowerPoint) and safety database tools
- Experience in medical writing for aggregate reports, literature screening, and signal detection
- Collaborative mindset for working in a global matrix environment
Key Responsibilities
- Author aggregate safety reports (PSURs, PBRERs, DSURs, PADERs)
- Prepare and maintain Risk Management Plans (RMPs)
- Contribute to Signal Management Reports
- Conduct literature searches and screening
- Perform data extraction, validation, and duplicate checks
- Generate and review line listings from safety databases
- Reconcile trackers and support ad-hoc PV activities
- Ensure timely delivery compliant with regulatory requirements
- Participate in audits and inspections as SME
- Contribute to SOPs, deviations, and CAPAs
Benefits/Perks
- Career growth in a fast-growing global organization
- Exposure to diverse pharmacovigilance projects and international clients
- Opportunities for professional development and learning
- Collaborative and supportive work culture
- Flexible remote work model with periodic Hyderabad office collaboration
- Competitive compensation and long-term career stability
How to Apply
Interested candidates can apply directly via ProPharma’s official careers portal using requisition ID JR 9433. For more pharma jobs and pharmaceutical careers across India, visit Pharma Recruiter.
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Verification: To confirm the legitimacy of this posting, you can view the original announcement on the ProPharma career page.
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Apply now and take your pharmacovigilance career to the next level with a leading global CRO!
Why You Should Join
ProPharma offers a supportive, innovation-driven culture where professionals contribute to meaningful patient safety outcomes. You’ll enjoy long-term career stability, continuous learning, global exposure, and recognition in a compliant, high-performance environment that values quality and collaboration. Join a company dedicated to accelerating life-changing therapies while advancing your expertise in pharmacovigilance.
FAQs
Q1: What is the minimum experience required for the Pharmacovigilance Scientist role?
A: Minimum 2+ years of hands-on experience in Pharmacovigilance, particularly in aggregate reports or signal management.
Q2: Is this a fully remote position?
A: Yes, it is primarily remote; however, candidates near Hyderabad are preferred for periodic office collaboration.
Q3: What qualifications are needed for this pharma job?
A: Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Nursing, or a related scientific field.
Q4: How does this role support career growth?
A: It offers exposure to global projects, medical writing, regulatory compliance, and opportunities to work as a Subject Matter Expert in audits and inspections.
