The pharmaceutical industry continues to grow rapidly, and pharmacovigilance is one of the most in-demand career paths for fresh graduates. A new opportunity has opened for entry-level candidates in Thane, offering a strong foundation in drug safety and regulatory practices.
If you hold a B.Pharm or M.Pharm degree and are looking to kickstart your career, this role provides hands-on exposure to real-world pharmacovigilance operations.
๐ข Job Overview
Job Title
Pharmacovigilance Associate (Freshers)
Location
Thane (Work From Office)
Experience
Freshers / Entry-Level Candidates
Qualification
- B.Pharm
- M.Pharm
๐ผ Key Responsibilities
As a Pharmacovigilance Associate, you will be responsible for ensuring drug safety through proper monitoring and reporting processes.
- Perform Adverse Event Case Processing (ICSR processing)
- Enter and manage safety data in pharmacovigilance databases
- Review and analyze safety reports with high accuracy
- Ensure compliance with global regulatory guidelines
- Support ongoing pharmacovigilance activities and reporting
๐ง Required Skills
Candidates should have a strong academic base along with the following skills:
- Basic understanding of safety databases
- Knowledge of pharmacovigilance processes (preferred)
- Strong analytical and attention-to-detail abilities
- Good communication and documentation skills
- Ability to handle data with accuracy and responsibility
๐ Preferred Candidate Profile
- Strong academic background in pharmacy
- Interest in drug safety and regulatory affairs
- Willingness to work in a structured office environment
- Quick learner with a proactive attitude
๐ฐ Salary & Benefits
- Estimated Salary: โน2.5 LPA โ โน4 LPA
- Hands-on training in pharmacovigilance
- Exposure to global drug safety standards
- Career growth opportunities in regulatory and safety domains
- Professional work environment
๐ฉ How to Apply
Interested candidates can directly share their updated resume via email:
Email: asharma@crescentpharma.com
Make sure your resume highlights your academic qualifications and any relevant knowledge of pharmacovigilance.