As a Pharmacovigilance Services New Associate, you will be part of Accenture’s Life Sciences R&D vertical. Your responsibilities will include managing various aspects of pharmacovigilance, such as:
- Case identification, data entry, MedDRA coding, and processing.
- Managing case submissions and follow-ups for Individual Case Safety Reports (ICSRs) in the safety database.
- Handling the Affiliate Mailbox and reconciling reports per process.
- Performing all written follow-up attempts for both Serious and Non-serious cases.
Key Responsibilities:
- Solve routine problems using general guidelines and precedents.
- Execute tasks with detailed instructions provided by your supervisor.
- Contribute as an individual within a team, focusing on a narrow scope of work.
- Ensure compliance with client guidelines and applicable global regulatory requirements.
What We Are Looking For:
- Technical Skills: Pharmacovigilance & Drug Safety Surveillance, Clinical Data Management.
- Personal Attributes: Adaptability, flexibility, ability to perform under pressure, commitment to quality.
- Communication: Strong written and verbal communication skills.
- Teamwork: Ability to work well in a team environment.
Additional Information:
- Shift: Rotational shifts may be required.
- Supervision: Decisions made in this role will impact your own work and will be closely supervised.
