Location: Karnataka, Noida, Uttar Pradesh, India
End Date for Applications: 30th October 2024
About Clarivate
Clarivate is a global leader dedicated to accelerating the lifecycle of innovation. Our mission is to help customers tackle some of the world’s most complex challenges by providing actionable insights and information, enabling the transition from ideas to impactful inventions across science and intellectual property sectors.
Position: Manager, Pharmacovigilance
Job Description: The Pharmacovigilance Manager will oversee all literature screening activities within the Pharmacovigilance department. This role demands advanced expertise in pharmacovigilance, including literature screening methodologies, signal detection, and risk assessment, along with strong team management skills.
Key Responsibilities:
- Oversee and coordinate all literature screening activities, including search strategy development, process management, and data extraction.
- Assist with operational excellence and support recruitment for the literature review team.
- Conduct in-house training for new recruits and organize regular refresher training sessions.
- Manage communication with customers regarding business operations.
- Assess trainee performance and maintain comprehensive training records for audits.
- Ensure accuracy and consistency in data extraction and documentation.
- Analyze literature data to identify potential safety signals and emerging risks.
- Conduct comprehensive risk assessments of identified safety signals.
- Develop strategies for systematic literature screening relevant to pharmaceutical products.
- Establish best practices and SOPs for literature screening activities in compliance with regulatory requirements.
- Collaborate with cross-functional teams for risk mitigation and management.
- Mentor and develop the Literature Screening team, conducting regular performance reviews.
- Act as a backup for the Senior Manager of Pharmacovigilance when required.
Candidate Profile:
- Education: Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Nursing, or related field. An advanced degree (PharmD, MD, PhD) is preferred.
- Experience: Minimum of 10 years in pharmacovigilance or related fields within the pharmaceutical industry, with extensive experience in literature screening.
- Knowledge: In-depth understanding of pharmacovigilance principles, adverse event reporting, signal detection methodologies, and risk assessment principles. Familiarity with regulatory requirements (e.g., ICH, GVP) is essential.
Additional Information:
- Functional Area: Life Sciences & Healthcare
- Experience Required: 10+ years in the field
If you’re looking to make an impact in the field of pharmacovigilance and join a team dedicated to improving patient safety, apply by 30th October 2024.