Accenture, a global leader in digital, cloud, and life sciences operations, is hiring for three major life sciences positions:

• Clinical Data Services Associate
• Life Science Regulatory Services Associate
• Pharmacovigilance Services Associate

These roles are ideal for B.Pharm, M.Pharm, MSc, and BE graduates with 1–3 years of experience looking to grow in clinical research, regulatory operations, data management, and drug safety surveillance.
Accenture offers excellent career development, global project exposure, and the opportunity to work across leading biopharma clients.

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1. Clinical Data Services Associate – Mumbai

Key Responsibilities

• Work on SAS Clinical and CDISC SDTM standards.
• Validate clinical databases, UAT execution, and edit check testing.
• Identify protocol deviations and perform CRF/eCRF–based checks.
• Support clinical data management projects and data integration workflows.
• Maintain compliance with Accenture values and client expectations.

Qualifications

• BE / MSc / B.Pharm
• 1–3 years in clinical data management, SAS clinical, or CDISC
• Strong analytical, communication & teamwork skills
• Ability to work in rotational shifts

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2. Life Science Regulatory Services Associate – Bengaluru

Key Responsibilities

• Perform eCTD publishing, bookmarking, and hyperlinking activities.
• Support global regulatory submissions such as CMC, Ad-Promo, SPLs, Amendments & LCM.
• Conduct document QC, transform source documents, and verify submission components.
• Coordinate essential regulatory documentation as per ICH & global guidelines.

Qualifications

• B.Pharm
• 0–1 year in regulatory publishing, eCTD operations, or document QC
• Strong attention to detail & adherence to submission standards
• Available for rotational shifts

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3. Pharmacovigilance Services Associate – Chennai

Key Responsibilities

• Manage the affiliate mailbox and perform reconciliation processes.
• Handle ICSR case intake, MedDRA coding, processing, submissions & follow-ups.
• Ensure compliance with global PV regulations and client SOPs.
• Support both serious and non-serious case activities.

Qualifications

• B.Pharm / M.Pharm
• 1–3 years in Pharmacovigilance or Drug Safety Database operations
• Knowledge of MedDRA, case processing & safety regulations
• Ability to work in rotational shifts

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Why Join Accenture?

• Work with global pharmaceutical and biotechnology clients
• Exposure to advanced clinical and regulatory technologies
• Strong learning culture & career progression
• Inclusive and equal-opportunity workplace
• Opportunities across clinical research, safety, regulatory & data sciences

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How to Apply

Application Link for Clinical Data Services Associate

Application Link for Regulatory Services Associate

Application Link for Pharmacovigilance Associate