Accenture is a global professional services company that excels in digital, cloud, and security solutions. With a workforce of 699,000 people across more than 120 countries, we offer unmatched expertise across 40 industries, helping clients navigate change and drive innovation. Our Life Sciences R&D vertical plays a crucial role in supporting the world’s leading biopharma companies to enhance patient outcomes.
Position Summary
As a Pharmacovigilance Services Associate, you will contribute to our Pharmacovigilance & Drug Safety Surveillance team. Your responsibilities will involve managing case identification, data entry, MedDRA coding, and case processing, all while ensuring compliance with client guidelines and global regulatory requirements.
Key Responsibilities
- Case Management: Create and manage Individual Case Safety Reports (ICSRs) in the safety database.
- Data Entry: Accurately enter data and perform MedDRA coding for both Serious and Non-serious cases.
- Follow-Up: Conduct follow-up communications and reconciliation of reports as per established processes.
- Collaboration: Work closely with your team and supervisors to address routine problems using general guidelines.
- Documentation: Ensure all activities are documented per client requirements and regulatory standards.
- Rotational Shifts: Be prepared to work in rotational shifts as needed.
Qualifications
- Education: Bachelor’s degree in Pharmacy, Physiotherapy, or BSc in Nursing.
- Experience: 0 to 3 years of relevant experience in pharmacovigilance or drug safety.
- Skills:
- Ability to perform under pressure and meet deadlines.
- Strong team collaboration and adaptability.
- Quick learning agility for new processes and tools.
What We Offer
- A dynamic work environment that fosters collaboration and innovation.
- Opportunities for professional growth and development within the life sciences sector.
- A chance to make a meaningful impact in patient safety and drug development.
