Pharmacovigilance Job Opening at Accenture | B Pharmacy Freshers can Apply
If you are searching for a Pharma Freshers Job or a Pharmacovigilance Job, this opportunity as a Pharmacovigilance Services New Associate, Chennai, is an excellent starting point for your career. Accenture is hiring freshers and early professionals for its Life Sciences R&D vertical, offering hands-on exposure in drug safety surveillance, case processing, and global pharmacovigilance operations.
- Role: Pharmacovigilance Services New Associate
- Job No. AIOC-S01649704
- Location: Chennai
About the Company
Accenture is a leading global professional services company specializing in digital, cloud, security, strategy, consulting, technology, and operations services. With a workforce of over 784,000 professionals serving clients across more than 120 countries, Accenture helps organizations drive innovation, improve performance, and accelerate business transformation through advanced technology and human ingenuity.
Job Description
- Work within the Life Sciences R&D team supporting global biopharmaceutical companies.
- Help improve patient outcomes by connecting scientific expertise with patient-focused insights.
- Monitor the safety and effectiveness of medicines throughout their lifecycle.
- Detect, assess, and prevent adverse drug reactions (ADRs) and other safety concerns.
- Collect and analyze safety data from:
- Clinical trials
- Healthcare professionals
- Patients
- Regulatory databases
- Identify potential risks associated with pharmaceutical products.
- Support compliance with global regulatory requirements and safety guidelines.
- Assist in preparing safety reports and maintaining pharmacovigilance documentation.
- Contribute to protecting patient health and ensuring public confidence in medicines.
- Play a key role in helping safe and effective treatments reach patients worldwide.
Key Responsibilities
- Identify and process Individual Case Safety Reports (ICSRs) from various sources.
- Enter and maintain accurate case data in the pharmacovigilance safety database.
- Perform MedDRA coding for adverse events, medical conditions, and related information.
- Review and process safety cases according to client requirements and standard procedures.
- Prepare and submit ICSRs within regulatory timelines.
- Conduct follow-up activities to obtain missing or additional case information.
- Ensure compliance with global pharmacovigilance regulations and client guidelines.
- Maintain high-quality, accurate, and complete safety documentation.
Qualifications
- Bachelor of Pharmacy or Related Field
- Years of Experience: 0 to 1 years
Preferred Skills
- Ability to perform under pressure
- Ability to work well in a team
- Adaptable and flexible
