As a Pharmacovigilance Services Associate, you will be part of our Life Sciences R&D vertical. Your responsibilities will include managing case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for Individual Case Safety Reports (ICSRs) in the safety database according to client guidelines and global regulatory requirements.
Key Responsibilities:
- Manage the Affiliate Mailbox and reconcile reports as per process.
- Perform all written follow-up attempts for both Serious and Non-serious cases.
- Create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs.
- Work under pressure and display agility for quick learning.
- Commit to quality and prioritize workload effectively.
- Solve routine problems using general guidelines and precedents.
- Interact mainly within your team and with your direct supervisor.
- Make decisions that impact your own work within a focused scope of tasks.
- The role may require working in rotational shifts.
Qualifications:
- Bachelor of Pharmacy, Bachelor in Physiotherapy, or BSc Nursing.
- 1 to 3 years of relevant experience.
Skills Required:
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- Ability to perform under pressure.
- Agility for quick learning.
- Commitment to quality.
- Effective prioritization of workload.
