Pharmacovigilance Coordinator

Why This Role Matters
Pharmacovigilance Coordinators are central to ensuring patient safety through efficient case management, regulatory compliance, and real-time workflow monitoring. In global drug safety operations, timely adverse event reporting and adherence to GVP and FDA regulations directly influence regulatory trust, product continuity, and public health protection.

Job Description
ProductLife Group is hiring a Pharmacovigilance Coordinator (Remote – India, Full-Time). The role focuses on pharmacovigilance workflow case management, adverse event reporting oversight, safety compliance monitoring, and coordination of global drug safety operations. This opportunity is ideal for professionals with 3–4+ years of hands-on PV experience seeking international exposure.

Key Features of the Role:
• Remote position (India-based)
• Full-time employment
• 3–4+ years experience required
• Exposure to global safety standards
• Focus on workflow optimization and compliance
• International regulatory environment

Responsibilities
• Monitor real-time pharmacovigilance workflow performance
• Optimize task distribution and resource allocation
• Track case processing timelines and ensure compliance with deadlines
• Ensure proper assignment of safety cases
• Collaborate with operational and development teams
• Provide technical support and cross-training
• Investigate workflow issues and implement corrective solutions
• Analyze performance metrics for workflow improvement
• Coordinate safety-related projects
• Maintain structured documentation in compliance with global standards

Required Qualifications
• Degree in Life Sciences or higher
• Experience in pharmacovigilance workflow case management
• Hands-on exposure to adverse event reporting and causality assessment
• Knowledge of GVP guidelines and FDA regulations
• Understanding of cosmetic safety regulations
• Experience in SDEA/PVA interpretation

Educational Requirements:
• B.Pharm, M.Pharm, Pharm.D
• MSc, BSc (Life Sciences) or higher qualification

Experience and Skills:
• 3–4+ years in Pharmacovigilance operations
• Strong understanding of global regulatory safety requirements
• Proficiency in Microsoft Office Suite
• Database management experience
• Analytical and problem-solving skills
• Project coordination and documentation expertise
• Strong communication and teamwork abilities
• High adaptability and accountability

Age Eligibility:
As per company norms

Salary Insights
Salary not disclosed. Competitive compensation aligned with industry standards and experience level.

Company Overview
ProductLife Group is a global life sciences consulting organization supporting pharmaceutical, biotech, and medical device companies in regulatory, pharmacovigilance, and quality compliance services. The company provides international exposure and opportunities to work on cross-border regulatory projects within a collaborative professional environment.

FAQs

Is this role fully remote?
Yes, this is a remote role based in India.

Is prior pharmacovigilance experience mandatory?
Yes, 3–4+ years of relevant pharmacovigilance workflow experience is required.

Is knowledge of GVP and FDA regulations necessary?
Yes, strong knowledge of GVP guidelines and FDA regulations is essential.

Does the role involve project coordination?
Yes, coordination and documentation of safety projects are part of the responsibilities.

How can candidates apply?
Interested candidates can apply via the provided link or send resumes

Application Tips
• Highlight hands-on ICSR and workflow management experience
• Mention experience with GVP, FDA, and SDEA/PVA interpretation
• Emphasize regulatory compliance exposure
• Showcase data tracking and performance analysis skills
• Keep resume focused on global pharmacovigilance experience