Pharmacovigilance Scientist Opening | ProPharma Careers
ProPharma is hiring for the position of Pharmacovigilance Scientist, an excellent opportunity for professionals with 2+ years of experience in pharmacovigilance and drug safety. This role is focused on aggregate safety report writing, signal management, literature review, and global PV compliance, making it ideal for candidates looking to advance their careers in regulatory safety and medical writing within pharmacovigilance.
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🏢 Company Overview
ProPharma is a global consulting organization providing services across pharmacovigilance, regulatory affairs, clinical research, and compliance. The company supports pharmaceutical and biotechnology clients across the full product lifecycle, ensuring patient safety and regulatory adherence. ProPharma promotes a diverse, inclusive, and collaborative work culture, encouraging innovation and professional growth.
📊 Internship Overview
- Company Name: ProPharma
- Job Role: Pharmacovigilance Scientist
- Employment Type: Full‑Time
- Experience Required: Minimum 2+ Years
- Functional Area: Pharmacovigilance / Drug Safety
- Job Location: As per business requirement
📋 What You Will Do
- Authoring and reviewing key safety reports, including:
- PSURs / PBRERs
- PADERs / Annual Reports / ACO
- DSURs
- Preparing and maintaining Risk Management Plans (RMPs)
- Contributing to Signal Management Reports
- Conducting literature searches, screening, and validity checks
- Performing duplicate checks using appropriate tools
- Generating and reviewing line listings (LLs) from safety databases
- Maintaining safety trackers and reconciling datasets
🎓 Who Can Apply
- Bachelor’s or Master’s degree in:
- Pharmacy
- Nursing
- Life Sciences
- Or related healthcare/scientific field
- Equivalent experience may also be considered
- Minimum 2+ years of experience in Pharmacovigilance
- Experience in one or more of the following:
- Aggregate report writing
- Literature review and screening
- Signal detection
- Prior experience in authoring or reviewing aggregate safety reports is highly preferred
🧠 Required Skills
- Strong analytical and problem‑solving abilities
- Excellent attention to detail with a quality‑focused approach
- Effective organizational and time management skills
- Ability to work in a global, matrix environment
- Strong medical writing and scientific communication skills
- Ability to interpret and summarize complex safety data clearly
⭐ Role Insight
The Pharmacovigilance Scientist role is a high‑impact position in drug safety operations. Professionals in this role contribute to global safety reporting, regulatory compliance, and risk management strategies. Experience in aggregate report writing, signal detection, and regulatory guidelines positions candidates for advanced PV roles, safety science positions, and leadership opportunities.
🎯 Suitable For
This Opportunity is ideal for:
- Pharmacovigilance professionals with 2+ years experience
- Candidates experienced in aggregate report writing and safety data analysis
- Drug safety specialists interested in global PV regulations
- Professionals aiming to move into medical writing or safety science roles
💰 Salary & Benefits
- Competitive salary ranging from ₹6–12 LPA
- Enjoy flexible remote work options
- Gain hands-on experience with global pharmacovigilance projects
- Build expertise in benefit-risk analysis and regulatory safety
- Be part of an inclusive, supportive, and collaborative team
💡 Preparation Tips
- Revise aggregate report formats (PSUR, PBRER, DSUR)
- Strengthen knowledge of global PV regulations
- Practice summarizing safety data and writing scientific content
- Be prepared to discuss real‑world safety case or signal handling scenarios
📈Growth Opportunities
With experience and performance, professionals can progress into roles such as:
- Senior Pharmacovigilance Scientist
- Safety Scientist / Signal Detection Specialist
- Aggregate Reporting Lead
- Pharmacovigilance Manager or Medical Writing Lead
ProPharma provides a strong platform for long‑term career development.
🔗 How To apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer: This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.
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📚 Career Guide
Career opportunities in PV
Prepare with Pharmacovigilance interview questions
❓ Frequently Asked Questions (FAQs)
1.Why should candidates consider joining ProPharma?
Exposure to global pharmacovigilance projects
Opportunity to enhance expertise in drug safety and regulatory compliance
Growth‑oriented and collaborative work culture
2.Is this role suitable for freshers?
No. This position requires prior experience (minimum 2 years) in pharmacovigilance or related areas.
3.What career growth can be expected?
Senior PV Scientist roles
Medical writing specialization
Signal management and risk evaluation
