ProPharma Hiring Pharmacovigilance Safety Scientist

Pharmacovigilance Safety Scientist Openings | ProPharma India

Apply for Pharmacovigilance Safety Scientist role at ProPharma, India. Open for B.Pharm, M.Pharm, Nursing, Life Sciences graduates with 2+ years experience.

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ProPharma is seeking experienced Pharmacovigilance Safety Scientists for its Benefit-Risk team in India. This full-time position offers a chance to work with one of the world’s leading providers of regulatory, compliance, and clinical research solutions. If you are passionate about improving patient safety, data analysis, and contributing to drug safety excellence, this role is for you.

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Company Overview

For over 20 years, ProPharma has been advancing health and wellness by supporting pharmaceutical, biotech, and medical device companies in achieving regulatory success. With its advise-build-operate model, the organization provides full lifecycle consulting solutions across regulatory sciences, clinical research, pharmacovigilance, medical information, and R&D technology.

ProPharma is a global leader trusted by top healthcare innovators. Its culture of excellence, collaboration, and inclusion ensures employees thrive professionally while contributing to meaningful advancements in medical science.

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Job Role & Responsibilities

As a Pharmacovigilance (PV) Safety Scientist, you will play a critical role in supporting global pharmacovigilance and regulatory deliverables, ensuring compliance, accuracy, and timeliness. Key responsibilities include:

• Authoring aggregate safety reports such as PSURs, PBRERs, PADERs, DSURs, and Annual Reports for global health authorities.
• Drafting and maintaining Risk Management Plans (RMPs) and Signal Management Reports.
• Conducting literature searches, data validation, and scientific documentation for ongoing projects.
• Generating and verifying Line Listings (LL) from safety databases.
• Ensuring regulatory compliance and high-quality documentation aligned with FDA, EMA, and ICH-GCP guidelines.
• Supporting ad-hoc PV projects, deviation tracking, and CAPA documentation.
• Collaborating with internal teams and senior PV Scientists to maintain operational excellence.
• Providing scientific input on safety data, medical evaluation, and product benefit-risk assessments.

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Eligibility / Qualifications

Educational Background:

• Bachelor’s or Master’s degree in Pharmacy, Nursing, Life Sciences, Biotechnology, Biochemistry, or related healthcare disciplines.

Experience:

• Minimum 2+ years of experience in pharmacovigilance, particularly in medical writing, literature search, or signal detection.
• Hands-on experience with aggregate report authoring, quality documentation, and regulatory submissions.
• Strong analytical, writing, and presentation skills with excellent attention to detail.

Technical Skills:

• Proficiency in MS Office (Word, Excel, PowerPoint) and familiarity with pharmacovigilance databases.
• Understanding of global drug safety regulations (FDA, EMA, ICH-GCP).
• Ability to manage large data volumes and derive concise, accurate scientific summaries.

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Location & Work Type

Location: India (Remote / Office-based options available)
Type: Full-time
Department: Benefit-Risk / Pharmacovigilance

Salary is competitive and commensurate with experience. ProPharma also provides an inclusive environment with benefits such as healthcare coverage, professional development programs, and work-life balance support.

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Application Process

Interested candidates can apply directly on the ProPharma career portal. All applications are personally reviewed by a member of the recruitment team—no AI or automated screening tools are used.

Apply Now on ProPharma Website

Note: ProPharma does not accept unsolicited resumes from third-party recruiters. For transparency and fairness, all applicants receive a definitive outcome, whether selected or not.

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Why Join ProPharma?

• Global exposure to high-impact projects across pharma, biotech, and medical device sectors.
• Continuous learning opportunities and cross-functional collaboration.
• Supportive and inclusive work culture that values diversity, equity, and innovation.
• Work that directly contributes to improving patient safety and public health.

ProPharma’s mission is simple yet powerful: Empower life sciences organizations to deliver safer, more effective therapies faster.

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FAQs – Pharmacovigilance Safety Scientist at ProPharma

Q1. Who can apply for the Pharmacovigilance Safety Scientist role?
Candidates with B.Pharm, M.Pharm, Nursing, or Life Science backgrounds and at least 2 years of PV experience can apply.

Q2. Is prior experience in aggregate report authoring mandatory?
Yes, candidates should have hands-on experience in preparing PSURs, DSURs, or RMPs.

Q3. What is the work environment like at ProPharma?
ProPharma promotes collaboration, innovation, and inclusion, ensuring each employee can grow and make an impact.

Q4. What are the career growth opportunities?
Employees can advance into roles like Senior PV Scientist, Safety Lead, or Regulatory Writer based on performance and expertise.

Q5. How can I apply?
Apply through the official ProPharma Career Portal before the position closes.

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Markdown Summary Table

Company	ProPharma Group
Vacancies	Pharmacovigilance Safety Scientist (Benefit-Risk)
Required Education	B.Pharm, M.Pharm, Nursing, Life Sciences
Experience	Minimum 2+ years in Pharmacovigilance