Job Opportunity: Clinical Data Management & Pharmacovigilance Professionals

Job Summary

Accenture is currently seeking dedicated professionals to join our Life Sciences R&D team in Bengaluru. We are hiring for multiple positions within Clinical Data Management and Pharmacovigilance (Drug Safety). These roles offer an exceptional opportunity to build a long-term career in clinical research, drug safety operations, and regulatory services while working with top global pharmaceutical organizations. We welcome applications from both freshers and experienced professionals (1–8 years) with a background in Life Sciences or Pharmacy.

Open Positions

1. Clinical Data Services Associate

• Experience: 1–3 Years
• Domain: Clinical Data Operations (External Data Acquisition)

2. Pharmacovigilance Services Associate (Drug Safety)

• Experience: 1–3 Years
• Domain: ICSR Processing, Drug Safety Surveillance

3. Pharmacovigilance Services Senior Analyst

• Experience: 5–8 Years
• Domain: Advanced PV, Case Processing, and Team Leadership

Responsibilities

Clinical Data Roles

• Manage clinical data collection, validation, and reconciliation processes.
• Oversee external vendor data integration, including laboratory and imaging data.
• Draft and maintain essential documentation, including Protocol Specific Addenda (PSA), Data Transfer Specifications (DTS), and Interchange Format Agreements.
• Provide ongoing support for database builds and clinical reporting.
• Ensure full compliance with regulatory standards, specifically ICH-GCP guidelines.

Pharmacovigilance Roles

• Manage the end-to-end Individual Case Safety Report (ICSR) lifecycle.
• Execute case intake, data entry, MedDRA coding, and final submission processes.
• Conduct follow-up activities and provide support for signal detection.
• Maintain rigorous compliance with global pharmacovigilance regulations.
• Utilize industry-standard safety databases (such as Argus or ARISg) to document and track safety data.

Requirements

• Education: A Bachelor’s or Master’s degree in Life Sciences or B.Pharm/M.Pharm (specific to the role).
• Knowledge: A strong foundational understanding of Clinical Data Management or Pharmacovigilance workflows.
• Communication: Excellent interpersonal skills with the ability to engage effectively with global stakeholders.
• Professional Skills: Proven ability to manage multiple priorities, work efficiently under tight deadlines, and collaborate within a team-oriented environment.
• Flexibility: Adaptability to work in rotational shifts as required by project needs.

Benefits of Working at Accenture

Joining our Life Sciences team means becoming part of a global network operating in over 120 countries. You will benefit from:

• Industry Exposure: Gain direct experience with real-world clinical trials and complex safety data workflows for top-tier pharmaceutical clients.
• Technological Access: Work with cutting-edge AI, data analytics, and cloud-driven healthcare solutions.
• Career Growth: Benefit from a structured career path within the Life Sciences domain.
• Learning Ecosystem: Access continuous professional development and real-time project exposure that sharpens your technical and leadership skills.

How to Apply

We invite interested candidates to review the specific requirements for each role and submit their applications through the official Accenture careers portal. Please ensure your resume is updated to highlight your relevant experience in clinical data or drug safety.

• To apply for Clinical Data Services Associate: Click Here
• To apply for Pharmacovigilance Services Associate: Click Here
• To apply for Pharmacovigilance Services Senior Analyst: Click Here

Accenture is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.