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Role Overview
As a Pharmacovigilance Services Associate, you will be aligned with our Life Sciences R&D vertical, which supports a wide range of services, including clinical trials, regulatory services, and pharmacovigilance solutions. Your primary responsibilities will involve managing the Affiliate Mailbox, reconciling reports, and processing both Serious and Non-serious cases. This role is critical in helping leading biopharma companies improve patient outcomes by merging scientific expertise with insights into patient experiences.
Key Responsibilities
- Manage the Affiliate Mailbox and ensure effective communication.
- Reconcile reports according to established processes.
- Perform 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 Individual Case Safety Reports (ICSRs) in the safety database, in compliance with client guidelines and global regulatory requirements.
- Analyze and solve lower-complexity problems with moderate supervision.
- Collaborate with peers within Accenture and update supervisors as needed.
- Work on a variety of tasks with moderate instructions on daily activities and detailed guidance on new assignments.
- Potential to work in rotational shifts.
Qualifications
- Education: Any graduation.
- Experience: 1 to 3 years of experience in Pharmacovigilance Operations, Drug Safety Surveillance, or related fields.
What We’re Looking For
- Strong analytical and problem-solving skills.
- Ability to work effectively as an individual contributor within a team environment.
- Basic exposure to client interactions and management.
- Willingness to learn and adapt to new challenges.
Apply Now!
If you are passionate about improving patient safety and outcomes and meet the qualifications outlined above, we encourage you to apply for the Pharmacovigilance Services Associate position at Accenture.