You will be aligned with Accenture’s Life Sciences R&D vertical, covering services across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees in this span are part of the sub-offerings – Clinical, Pharmacovigilance & Regulatory – helping the world’s leading biopharma companies bring their vision to life by improving outcomes through patient-centric approaches.
Key responsibilities include:
- Management of the Affiliate Mailbox
- Reconciliation of reports per process
- Performance of all written follow-up attempts for both Serious and Non-serious cases
- Creation and management of case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements.
Roles and Responsibilities
- Analyze and solve increasingly complex problems.
- Daily interactions with peers within Accenture and occasional interaction with clients and/or Accenture management.
- Minimal instruction on daily work/tasks and moderate instruction on new assignments.
- Decisions impact your work and may impact the work of others.
- Work as an individual contributor and/or oversee a small team.
- Role may require working in rotational shifts.
