Pharmacovigilance professionals perform pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations.
About You - Education, Experience, Skills
- Bachelor's degree or equivalent in Pharmacy, Life Sciences, Nursing, or related field
- Minimum 7 Years of Relevant Experience
- Experience with commercial and client-specific biomedical literature databases.
- Related experience in drug safety/ pharmacovigilance is required
- Writing skills to support the creation of succinct, accurate, and precise summaries and working knowledge of biomedical terminology, drugs, and therapeutic areas
It would be great if you also had . . .
- Certification from a professional medical writer’s association
- Effective time management skills
- Excellent English written and verbal communication skills
- Adherence to SOP and Policies
What will you be doing in this role?
- Establish best practices and standard operating procedures (SOPs) for literature screening activities, ensuring compliance with regulatory requirements and industry standards.
- Oversee and coordinate all literature screening activities with a focus on quality and accuracy, including search strategy development, screening process management, and data extraction.
- Ensures effective communication of findings to stakeholders and collaboration with cross-functional teams for safety updates and risk management.
- Collaborate with cross-functional teams to develop and implement risk mitigation measures as needed.
- Set clear goals and objectives aligned with departmental and organizational objectives and lead the creation of training program for new recruits and regular refresher sessions for the entire team.
- Assess the performance of trainees and keep training records and documentation in a state ready for audit.
About Team:
Pharmacovigilance team at Clarivate provides services to multiple global customers covering all therapeutic areas. It provides a supportive working environment with personalized training, and opportunities to engage in different aspects of pharmacovigilance and customer engagement
Hours of Work
The team is based out of India (Bangalore or Noida ) and works 9:am IST to 6:00PM IST OR 11:00 AM to 8:00 PM (Mon-Friday) with Hybrid work mode
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At Clarivate, we are committed to providing equal employment opportunities for all qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.