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Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

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.

Application Link

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