Clarivate Hiring M Pharma Graduates | Apply for Pharmacovigilance Specialist Role
Clarivate is seeking a dedicated Associate Pharmacovigilance Specialist to join its Life Sciences & Healthcare division. This hybrid role presents a unique opportunity to collaborate with global pharmacovigilance experts, involving tasks such as literature monitoring, adverse event reporting, and data analysis. If you are looking for M Pharma Jobs and have a background in life sciences with a passion for patient safety, this is your chance to contribute to meaningful drug safety research and reporting.
- Job Position: Associate Pharmacovigilance Specialist
- Job ID: JREQ133625
About the Company
Clarivate is a global leader in providing trusted insights and analytics to accelerate innovation across industries, particularly in the Life Sciences and Healthcare sectors. The company’s mission is to empower organizations with accurate, data-driven solutions that improve decision-making and enhance public health outcomes. For professionals seeking M.Pharm jobs, Clarivate offers numerous opportunities.
Job Description
As an Associate Pharmacovigilance Specialist at Clarivate, you will perform a wide range of pharmacovigilance services, including biomedical literature monitoring, adverse event assessment, and data abstraction. This role requires a deep understanding of medical terminology, pharmacovigilance regulations, and therapeutic areas. If you are interested in M.Pharm jobs, you will contribute to drug safety reporting processes and ensure compliance with global standards.
Key Responsibilities
- Monitor biomedical literature and assess content for adverse event reporting.
- Perform indexing and abstracting of relevant biomedical data.
- Analyze and summarize biomedical case reports and studies accurately.
- Use scientific and medical knowledge to ensure compliance with pharmacovigilance regulations.
- Collaborate effectively with cross-functional teams in a hybrid work environment.
- Maintain flexibility and adaptability to meet changing client requirements.
Educational Qualification
Master’s Degree in Pharmacy is an essential qualification for many M Pharma Jobs.
Experience and Skills
- 1–2 years of experience in reviewing biomedical literature for adverse event reporting or equivalent combination of education and experience.
- Related experience in drug safety or pharmacovigilance is desirable.
- Strong analytical ability and excellent English communication skills.
- Proficiency in biomedical terminology, drugs, and therapeutic areas.
- Experience with commercial and client-specific biomedical literature databases.
- Ability to work both independently and collaboratively in a fast-paced setting.
- Basic computer literacy and adaptability to new technologies.
- Certification from a professional medical writer’s association.
- Experience in scientific or medical writing.
- Proven background in using commercial biomedical databases.
