Medical Reviewer Job at Cencora | Apply Now
Looking for a medical reviewer job in the pharmaceutical industry? This exciting opportunity at Cencora offers experienced professionals a chance to work in pharmacovigilance and drug safety. If you are searching for Cencora careers or a rewarding medicine job, this role in Noida could be your next big step.
Job Details
- Job Position: Medical Reviewer Case Processing
- Location: Noida, India
- Job ID: R2522052
- Employment Type: Full Time
About the Company
Cencora is a global healthcare company focused on creating healthier futures. The organization believes that its team members are at the heart of everything they do. Through innovation and dedication, Cencora continues to improve the lives of people and animals worldwide. If you are exploring Cencora careers, this is a great opportunity to be part of a purpose-driven company.
Job Description
This medical reviewer job involves conducting medical reviews of Individual Case Safety Reports (ICSRs) and ensuring accuracy in pharmacovigilance processes. The role requires strong knowledge of drug safety regulations and the ability to work within safety databases while maintaining compliance with global guidelines. This is an ideal medicine job for professionals with experience in pharmacovigilance.
Qualifications
- Degree in Medicine
- PG degree in any discipline is an advantage but not mandatory
Experience Required
- Minimum 8 years of relevant experience in Pharmacovigilance & Drug Safety
Skills & Knowledge
- Strong interpersonal and organizational skills.
- High sense of responsibility and dedication.
- Ability to work under pressure.
- Service-oriented mindset.
- Previous exposure to corporate environment, pharma and life sciences industry is an advantage.
- Good communication skills.
- Fluent in English (spoken and written)
Key Responsibilities
- Conduct initial assessment and Medical Review of ICSR’s into the safety database.
- Review and verify appropriate selection of adverse events from source documents.
- Check seriousness criteria, appropriate MedDRA code, suspect drug, concomitant medications, lab data, medical history, labelling, causality, review narrative and provide Company Causality Comment.
- Review and respond to any queries/comments from the Case Owner in the Safety database.
- Train and mentor PV associates on event capturing and general PV conventions as required.
- Acquire and maintain current knowledge of product and safety profiles across therapeutic areas.
- Escalate complex case issues on client products to Team Lead/Line Manager.
- Detail any follow-up information required and not already noted within the Safety database.
- Provide documentation of the review and case comments in Safety database in Medical Review workflow.
- Maintain good knowledge of databases, regulations, guidelines and SOP’s.
- Maintain strong GPVP and GCP knowledge while following ICH, EMA and FDA guidelines.
- Actively communicate and participate in internal project meetings.
- Participate in internal and external audits/inspections.
- Perform other drug safety related activities as assigned by management.
