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Accenture Hiring Clinical Data Management & Pharmacovigilance Roles (0–3 Yrs)

Job Opportunity: Clinical Data Management & Pharmacovigilance Professionals

Job Summary

Accenture is currently expanding its Life Sciences R&D team in Bengaluru and is inviting applications for multiple roles in Clinical Data Management (CDM) and Pharmacovigilance (PV). These positions are designed for dedicated B.Pharm graduates and BE candidates eager to build a high-impact career in clinical research, drug safety, and regulatory services. As part of a global leader in clinical trials and regulatory operations, successful candidates will contribute to real-world projects for top-tier pharmaceutical and biotech clients.

Open Positions

We are hiring for the following roles based on experience and academic background:

  1. Clinical Data Services Associate (Clinical Database Programming): Requires a BE degree and 1–3 years of experience. Proficiency in SAS, Cognos, J-Review, and EDC programming is essential.
  2. Clinical Data Services Associate (Clinical Data Management): Requires a B.Pharm degree and 1–3 years of experience, with a focus on clinical data validation and lab management.
  3. Pharmacovigilance Services New Associate: Open to B.Pharm freshers (0–1 years of experience).
  4. Pharmacovigilance Services Associate: Requires a B.Pharm degree and 1–3 years of experience.

Key Responsibilities

For Clinical Data Management Roles:

  • Manage data cleaning, discrepancy reviews, and efficient query resolution.
  • Develop and implement edit checks and validation scripts.
  • Conduct User Acceptance Testing (UAT) and comprehensive database validation.
  • Create and maintain CRF/ECRF guidelines and oversee SAE reconciliation.
  • Generate detailed analytical reports utilizing SAS, Cognos, and J-Review.

For Pharmacovigilance Roles:

  • Manage end-to-end Individual Case Safety Report (ICSR) processing.
  • Perform accurate MedDRA coding and data entry.
  • Handle case triage, follow-up communications, and regulatory submissions.
  • Ensure all processes remain in strict compliance with FDA, EMA, and global pharmacovigilance guidelines.

Requirements

  • Education: B.Pharm for PV and CDM roles; BE (relevant fields) for Database Programming roles.
  • Experience: 0–3 years of relevant experience (freshers are eligible for the PV New Associate position).
  • Technical Proficiency: Strong foundation in Clinical Data Management or Pharmacovigilance processes.
  • Soft Skills: Strong analytical, problem-solving, and communication skills. A detail-oriented mindset is essential for maintaining accuracy in clinical data and safety reporting.
  • Flexibility: Ability to work in rotational shifts.
  • Collaboration: Proven ability to work effectively within a team and communicate with stakeholders.

Why Join Accenture?

  • Global Exposure: Work on critical clinical trials and drug safety projects with a presence in over 120 countries.
  • Professional Growth: Access to industry-leading training in SAS, EDC, and safety database tools.
  • Career Advancement: Clear paths for professional development in CDM, PV, and regulatory domains.
  • Stability: Join a leading multinational corporation with a collaborative and innovative work culture.
  • Compensation: Competitive salary range of ₹3.5 LPA – ₹7.5 LPA, commensurate with experience and the specific role.

Job Location

Bengaluru, India.

How to Apply

Interested candidates should apply through the official Accenture careers portal. Please use the relevant links below based on the position you are applying for:

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