Navatio Pharma is looking for a dynamic Pharmacovigilance Project Manager at Hyderabad
In the ever-evolving pharmaceutical industry, Pharmacovigilance (PV) plays a crucial role in ensuring drug safety and regulatory compliance. If you’re an experienced professional in pharmacovigilance project management, we have an exciting opportunity for you! Navatio Pharma is looking for a dynamic Pharmacovigilance Project Manager to join our team in Hyderabad.
Why Join Navatio Pharma?
At Navatio Pharma, we are committed to delivering high-quality pharmacovigilance solutions to safeguard patient health worldwide. As part of our growing team, you will have the opportunity to work with leading experts in drug safety, regulatory affairs, and medical affairs. This role offers an excellent platform to advance your career while making a meaningful impact on global health.
Position: Pharmacovigilance Project Manager
📍 Location: Hyderabad
🎓 Education: B Pharm / M Pharm / MPH / MBA (Healthcare Management)
💼 Experience: 3-5 years in Pharmacovigilance Project Management
Key Responsibilities:
🔹 Act as the primary point of contact for internal and external stakeholders.
🔹 Build and maintain strong client relationships to ensure seamless project execution.
🔹 Define project scope, timelines, and objectives based on client agreements.
🔹 Oversee project activities, track progress, and ensure timely delivery of milestones.
🔹 Manage project budgets, resource allocation, and risk mitigation strategies.
🔹 Ensure adherence to regulatory requirements, SOPs, and quality standards.
🔹 Coordinate with cross-functional teams, including safety operations, regulatory affairs, and medical affairs.
🔹 Facilitate meetings, resolve project challenges, and ensure smooth project execution.
🔹 Support the preparation and submission of key safety documents (PADERs, PSURs, DSURs, RMPs).
🔹 Train and mentor team members on best practices in pharmacovigilance.
🔹 Assist with regulatory audits and implement corrective actions where necessary.
🔹 Stay updated with industry trends and regulatory changes.
Qualifications and Skills:
✔️ Strong experience in Pharmacovigilance Project Management (preferably in a CRO).
✔️ Bachelor’s degree in Pharmacy, Life Sciences, or Medicine (Master’s is a plus).
✔️ Expertise in ICSR processing, literature monitoring, signal management, and periodic reports.
✔️ Strong project management, team coordination, and client-handling skills.
✔️ Proficiency in MS Office & project management tools.
✔️ Excellent communication and multitasking abilities.
✔️ Ability to manage multiple projects while ensuring high-quality standards.
How to Apply?
📩 If you are passionate about drug safety and regulatory compliance, this is your chance to make a difference. Send your resume to hr@navatiopharma.com and be a part of our growing team!
📢 Join us and be a part of a dynamic team ensuring patient safety worldwide!
📩 Apply now or refer a suitable candidate!
📧 Email your resume to: hr@navatiopharma.com
