As a Pharmacovigilance Services Associate, you will be aligned with Accenture’s Life Sciences R&D vertical, focusing on clinical trials, regulatory services, and pharmacovigilance. Your role will be pivotal in monitoring and ensuring drug safety through case identification, data entry, and follow-up processes.
Key Responsibilities
- Manage affiliate mailboxes and reconcile reports as per processes.
- Perform written follow-ups for serious and non-serious cases.
- Create and manage cases, including data entry, MedDRA coding, and case processing.
- Handle ICSR submissions and follow-ups in compliance with client guidelines and global regulatory requirements.
- Solve routine problems by following established guidelines.
- Work as an individual contributor within a focused scope of tasks.
Required Skills
To thrive in this role, you need the following attributes:
- Ability to perform under pressure.
- Team collaboration skills.
- Adaptability and flexibility in dynamic environments.
- Quick learning capability and agility.
Qualifications
- Bachelor’s degree in Pharmacy, Physiotherapy, or Nursing.
- Experience in pharmacovigilance or related roles is advantageous but not mandatory (0–3 years).
Why Join Accenture?
Accenture offers a platform for growth and learning, with access to cutting-edge technologies and global projects. Here are some benefits of joining Accenture:
- Inclusive Culture: A workplace that values diversity and fosters innovation.
- Global Exposure: Collaborate with top pharmaceutical and healthcare companies worldwide.
- Learning Opportunities: Gain hands-on experience in pharmacovigilance and regulatory affairs.
- Career Growth: Structured career paths to help you excel.
