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A leading organization in the pharmaceutical safety sector has announced a new opening in its Pharmacovigilance Department for Regulatory Case Booking and Literature Screening roles. This is an excellent opportunity for fresh graduates and early-career professionals eager to build a strong foundation in drug safety, literature monitoring, and pharmacovigilance operations.
This permanent, work-from-office position in Ahmedabad, Gujarat, is ideal for candidates passionate about patient safety and regulatory compliance.
Key Responsibilities
- Perform Regulatory Case Booking with accuracy and compliance to global PV standards.
- Conduct systematic literature screening to identify safety-relevant data.
- Ensure adherence to pharmacovigilance guidelines, SOPs, and regulatory requirements.
- Support documentation activities, data entry, and workflow management.
- Collaborate with cross-functional teams to maintain PV quality and reporting efficiency.
Required Qualifications
Candidates with the following degrees are eligible to apply:
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- B. Pharm
- M. Pharm
- Pharm D
- M.Sc. (Life Sciences)
- B.Sc. (Life Sciences)
Freshers and early-career applicants are encouraged to apply.
Candidate Preference
Priority will be given to:
- Candidates residing in Ahmedabad
- Candidates residing in Gandhinagar
Benefits of Joining
- Hands-on experience in core pharmacovigilance operations.
- Exposure to real-time case processing and global regulatory requirements.
- Work with experienced PV professionals and develop industry-relevant competencies.
- Stable full-time role with growth opportunities.
- Work-from-office setup enabling structured learning and teamwork.
How to Apply
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