Hybrid Life Sciences Pharmacovigilance Job at ICON plc – Apply Online
Manager, Pharmacovigilance
Chennai, Trivandrum
JR126072
Drug Safety
ICON Full Service & Corporate Support
Hybrid: Office/Remote
About the role
Manager, Pharmacovigilance (Budgets & Proposals)
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Manager, Pharmacovigilance to join our diverse and dynamic team. As a Manager, Pharmacovigilance at ICON, you will be responsible for overseeing the pharmacovigilance activities, ensuring the safety and efficacy of clinical trial products throughout their lifecycle. Your role will involve managing a dedicated team, ensuring compliance with regulatory requirements, and fostering a culture of safety and quality within the organization.
What You Will Be Doing:
- Leading the pharmacovigilance team in the collection, evaluation, and reporting of adverse events, ensuring compliance with regulatory guidelines and internal standards.
- Developing and implementing pharmacovigilance processes and policies to enhance the efficiency and effectiveness of safety monitoring activities.
- Collaborating with clinical, regulatory, and quality assurance teams to ensure comprehensive safety assessments and timely reporting of safety data.
- Providing training and guidance to team members and stakeholders on pharmacovigilance regulations, practices, and procedures.
- Monitoring and analyzing safety data trends, preparing risk assessments, and presenting findings to relevant stakeholders.
- Ensuring that all pharmacovigilance activities are conducted in accordance with global regulatory requirements and internal quality standards.
Your Profile:
- Bachelor’s degree in life sciences, pharmacy, or a related field is preferred, with extensive experience in pharmacovigilance or drug safety management.
- Proven experience in managing pharmacovigilance teams and activities, with a thorough understanding of regulatory requirements and safety reporting standards.
- Strong analytical skills, with experience in assessing safety data and preparing safety reports for regulatory submission.
- Excellent leadership and organizational skills, with the ability to manage multiple projects and deliver results in a fast-paced environment.
- Exceptional communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external stakeholders.
- Detail-oriented, proactive, and committed to maintaining the highest standards of safety and quality in pharmacovigilance operations.
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