 Company: Accenture
Location: Plant 3, Godrej and Boyce Compound, LBS Marg, Vikhroli (W), Mumbai, Maharashtra, India
Employment Type: Full Time, Permanent
Industry Type: IT Services & Consulting
Department: Healthcare & Life Sciences
Role Category: Health Informatics
About Accenture
Accenture is a global professional services company with unmatched capabilities in digital, cloud, and security. With a workforce of over 514,000 across more than 120 countries, we deliver innovative solutions through Strategy and Consulting, Interactive, Technology, and Operations services. Our mission is to harness the power of change to create value and shared success for our clients, people, shareholders, partners, and communities.
Job Description
Position Overview: As a Pharmacovigilance Services Associate, you will be integral to our Life Sciences R&D vertical. You will support our efforts in pharmacovigilance and drug safety surveillance, assisting leading biopharma companies in enhancing patient outcomes through effective data management and regulatory compliance.
Key Responsibilities:
- Manage the Affiliate Mailbox and reconcile reports according to established processes.
- Conduct written follow-ups for both Serious and Non-serious cases.
- Create and manage case identification, data entry, MedDRA coding, case processing, and submissions for Individual Case Safety Reports (ICSRs).
- Adhere to client guidelines and global regulatory requirements in all case management activities.
- Collaborate effectively with team members and supervisors, contributing to a cohesive work environment.
- Solve routine problems using general guidelines and precedents.
- Participate in rotational shifts as required.
Qualifications
Educational Background:
- Bachelor’s degree in Pharmacy, Physiotherapy, or BSc in Nursing.
Experience:
- 0 to 3 years of relevant experience in pharmacovigilance, drug safety, or related fields.
Key Skills:
- Strong understanding of drug safety and pharmacovigilance processes.
- Proficiency in case processing and data entry.
- Familiarity with MedDRA coding and pharmacological principles.
- Knowledge of ICH-GCP guidelines and clinical trial protocols.
- Effective communication skills and the ability to work under pressure.
- Agility in learning and adapting to new challenges.
What We Are Looking For:
- Team-oriented individuals who can adapt to dynamic environments.
- Quick learners with a proactive approach to problem-solving.
- Ability to perform effectively under pressure while maintaining a focus on quality and compliance.
If you are ready to contribute to meaningful change in the life sciences sector and support patient safety through pharmacovigilance, we encourage you to apply!
