Pharmacovigilance Specialist / Lead PV Specialist at Clarivate
Position: Pharmacovigilance Specialist / Lead PV Specialist
- Organization: Clarivate
- Location: Noida, Uttar Pradesh, India
- Remote: Hybrid (Remote + On-site)
- Job ID: JREQ128594
- Industry: Life Sciences & Healthcare
Job Overview
Clarivate is hiring a Pharmacovigilance Specialist / Lead PV Specialist to join our dynamic Pharmacovigilance (PV) team. In this hybrid role, you will have the flexibility to work remotely while also engaging on-site when needed. You will be instrumental in conducting literature monitoring, assessing adverse event reports, and applying your expertise in scientific and medical terminology, drug safety, and pharmacovigilance regulations.
Key Responsibilities
As a Pharmacovigilance Specialist, your core responsibilities will include:
- Literature Monitoring: Analyze biomedical literature and internal drug safety alerts to identify relevant Individual Case Safety Reports (ICSRs) and safety information.
- Case Summary Writing: Create concise summaries of ICSRs and other safety-relevant data.
- Safety Assessments: Utilize drug labels during safety assessments and ensure drug safety reviews are completed in a timely manner.
- Drug Safety System Management: Track actions and assessments using a drug safety system.
- Literature Abstraction: Select and abstract relevant biomedical articles for the client’s product literature database.
- Regulatory Awareness: Stay informed about new drugs, therapeutic categories, and developments in biomedical terminology.
Required Qualifications
Candidates must possess the following qualifications to be considered for this role:
- Master’s Degree in Life Sciences, Health, or Biomedical Sciences (e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics).
- Degrees in Dentistry, Physiotherapy, or Nursing are a plus.
- At least 4 years of experience reviewing biomedical literature for adverse event reporting.
- Alternatively, 6 years of relevant experience with an information science degree.
- Proficiency in biomedical terminology, drugs, and therapeutic areas.
- Strong analytical skills to summarize case reports and studies.
- Database/Literature Search Experience: Ability to conduct detailed literature searches.
- Excellent communication skills (both verbal and written) and interpersonal skills.
- Strong ability to work collaboratively, manage tasks, and prioritize workload effectively.
Preferred Qualifications
While not mandatory, the following qualifications are preferred:
- Certification from a professional medical writer’s association.
- Experience with commercial and client-specific biomedical literature databases.
- Background in scientific/medical writing is a plus.
What We Offer
Joining Clarivate means being part of a supportive work environment with opportunities for growth and learning. We offer:
- Personalized Training: Tailored to help you succeed in the pharmacovigilance domain.
- Opportunities for Engagement: Work on various aspects of pharmacovigilance and contribute to customer upgrade planning if desired.
- Hybrid Work Model: Flexibility to work both remotely and on-site.
Work Schedule
- Full-Time, permanent position.
- Weekdays (Monday to Friday).
- Regular working hours, with a focus on achieving a work-life balance.
Equal Employment Opportunity
At Clarivate, we are committed to providing equal employment opportunities. We adhere to all applicable laws and regulations to ensure fairness in hiring, compensation, promotion, and employment terms. Diversity and inclusion are at the core of our culture, and we value a workplace where all employees are respected and empowered.
How to Apply
If you are passionate about pharmacovigilance and want to make a difference in life sciences and healthcare, apply now! Visit our official website or reach out to the HR team for more details on the application process.
Location
- Noida, Uttar Pradesh, India