Instagram
youtube
Facebook

Pharmacovigilance Project Manager

2-4 years
Not Disclosed
10 Nov. 18, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Pharmacovigilance Project Manager

Location: Hyderabad, India

Experience Required: 2–4 years in Pharmacovigilance Project Management (CRO experience preferred)

Education: B.Pharm / M.Pharm / MPH / MBA (Healthcare Management)

About the Role:
Navatio Pharma is seeking an experienced Pharmacovigilance Project Manager to oversee and drive PV projects efficiently, ensuring compliance with global regulatory requirements and high-quality delivery. The ideal candidate will act as the primary point of contact for clients and internal teams, managing project timelines, budgets, and resources while maintaining strong client relationships.

Key Responsibilities:

  • Serve as the main contact for project communications with clients and internal stakeholders.

  • Develop and manage project scope, objectives, timelines, and milestones aligned with client agreements.

  • Plan, track, and oversee project activities to ensure on-time delivery and successful execution.

  • Monitor project budgets, resource allocation, and timelines for optimal efficiency.

  • Prepare and present project progress reports for clients and internal stakeholders, including invoicing and performance tracking.

  • Ensure compliance with regulatory requirements, internal SOPs, and quality standards.

  • Facilitate project meetings, clearly communicate goals, and resolve project-related issues.

  • Coordinate with cross-functional teams such as safety operations, medical affairs, and regulatory affairs.

  • Support preparation and submission of safety reports, including PADERs, PSURs, DSURs, and other regulatory documents.

  • Train and mentor team members in pharmacovigilance processes, regulatory requirements, and best practices.

  • Prepare for and support audits and regulatory inspections, implementing corrective actions as needed.

  • Stay updated on emerging trends, regulations, and best practices in pharmacovigilance.

Qualifications & Skills:

  • Proven experience in Pharmacovigilance Project Management, preferably in a CRO environment.

  • Bachelor’s in Pharmacy, Life Sciences, or Medicine; Master’s is a plus.

  • Expertise in ICSR processing, PADERs, DSURs, PSURs, RMPs, signal management, and literature monitoring.

  • Strong project management, team coordination, and client-facing skills.

  • Proficiency in MS Office and project management tools.

  • Excellent communication, multitasking, and compliance handling capabilities.

  • Ability to manage multiple projects while maintaining high-quality standards.

Why Join Navatio Pharma:

  • Be part of a dynamic team committed to patient safety globally.

  • Opportunity to work across diverse pharmacovigilance projects with leading clients.

  • Professional growth through exposure to global PV regulations and best practices.

How to Apply:
Send your resume to hr@navatiopharma.com with the subject line “Pharmacovigilance Project Manager – Application.”

#Hiring #Pharmacovigilance #ProjectManager #LifeSciences #PharmaJobs #NavatioPharma