Pharmacovigilance job at Accenture Careers | Apply Now for Pharma Jobs | Pharmacovigilance New Service Associate Role
Are you seeking a rewarding Pharmacovigilance job that allows you to make a impact in the healthcare industry? Accenture is actively seeking a detail-oriented Pharmacovigilance Services Associate to join their renowned Life Sciences R&D vertical. As one of the most sought-after Pharma Jobs currently available, this role is perfect for professionals with a B.Pharm or M.Pharm degree who are passionate about monitoring drug safety. If you have 1 to 3 years of experience and want to grow your career with a global leader, this Pharmacovigilance job is the perfect next step.
- Job Title: Pharmacovigilance Services Associate
- Location: Bengaluru
About the Company
Accenture is a globally recognized professional services leader known for transforming how businesses operate through technology, innovation, and human expertise. Headquartered in Dublin, Ireland, Accenture operates across 120+ countries and serves clients in 40+ industries, including life sciences, healthcare, technology, finance, retail, energy, and more.
With a strong presence in India—including major hubs in Bengaluru, Hyderabad, Pune, Mumbai, Chennai, and Gurugram—Accenture Careers offers professionals the opportunity to work with world-class teams, cutting-edge platforms, and industry-leading clients. The company is also known for its commitment to digital transformation, cloud modernization, and AI-driven solutions, helping clients stay future-ready.
Job Description
You will work in the Life Sciences R&D team, supporting biopharma companies across areas like clinical research, pharmacovigilance, regulatory services, and patient support. Your role will be part of the Clinical, Pharmacovigilance & Regulatory team, helping improve patient outcomes by combining scientific knowledge with patient-focused insights.
In Pharmacovigilance Operations, your main job is to ensure the safety of medicines. This includes identifying, recording, coding (MedDRA), processing, submitting, and following up on safety cases (ICSRs) in safety databases, as per client and global regulatory guidelines. You will work with safety data from clinical trials, doctors, and patients to help monitor and prevent adverse drug effects, protecting public health and patient safety.
Key Responsibilities
In this role, you are required to perform the following:
- Solve routine problems, largely through precedent and referral to general guidelines.
- Interact primarily within your own team and with your direct supervisor.
- Follow detailed to moderate levels of instruction on daily work tasks and detailed instruction on new assignments.
- Make decisions that impact your own work.
- Act as an individual contributor as a part of a team, with a predetermined, focused scope of work.
Qualifications
- Education: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm).
- Experience: 1 to 3 years.
- Skill Required: Pharmacovigilance Operations – Pharmacovigilance & Drug Safety Surveillance.
