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Clinical Data Services Associate

Accenture
0-3 years
Not Disclosed
Bangalore, India
2 June 2, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data Services Associate

Location: Bengaluru, India
Job Type: Full-Time
Experience: 0–3 Years
Job ID: AIOC-S01647299

About the Role

We are seeking a motivated Clinical Data Services Associate to join our Life Sciences & R&D team. The ideal candidate will support clinical trial operations through accurate data management, medical monitoring support, protocol review, and clinical data quality activities. This role offers an excellent opportunity to work with global biopharmaceutical clients and contribute to the development of innovative healthcare solutions.

Key Responsibilities

  • Support clinical data management activities for ongoing clinical trials.

  • Review, validate, and maintain clinical trial data to ensure accuracy, completeness, and compliance.

  • Assist in medical monitoring activities and safety oversight processes.

  • Create, review, and validate protocol requirement specifications in accordance with applicable SOPs and regulatory guidelines.

  • Identify, investigate, and resolve routine data discrepancies.

  • Ensure clinical data quality through data review and validation procedures.

  • Collaborate with cross-functional teams including Clinical Operations, Pharmacovigilance, Regulatory Affairs, and Medical Affairs.

  • Maintain compliance with GCP, ICH guidelines, SOPs, and regulatory requirements.

  • Prepare and maintain study documentation and reports as required.

Required Qualifications

  • BE / Bachelor's Degree in Pharmacy (B.Pharm)

  • Master's Degree in Pharmacy (M.Pharm)

  • Freshers with relevant internships or candidates with up to 3 years of experience may apply.

Required Skills

  • Clinical Data Management

  • Medical Monitoring

  • Clinical Trial Operations

  • Data Validation & Quality Review

  • Protocol Review & Documentation

  • Good Clinical Practice (GCP) Knowledge

  • Strong Analytical & Problem-Solving Skills

  • Excellent Written and Verbal Communication

  • Attention to Detail

Preferred Skills

  • Understanding of Clinical Research and Drug Development Processes

  • Knowledge of Clinical Data Management Systems (CDMS)

  • Familiarity with Regulatory and Compliance Requirements

  • Ability to work effectively in a team environment

What We Are Looking For

  • Adaptable and flexible mindset

  • Strong analytical and problem-solving abilities

  • Effective communication skills

  • Ability to learn quickly and work in a fast-paced environment

  • Commitment to quality and compliance

Working Conditions

  • Individual contributor role within a collaborative team environment.

  • Detailed guidance and training will be provided for daily tasks and new assignments.

  • May require working in rotational shifts based on business requirements.

About Accenture

Accenture is a leading global professional services company specializing in digital, cloud, security, technology, consulting, and operations services. With a presence in more than 120 countries and a workforce of over 784,000 professionals, Accenture helps organizations drive innovation and create sustainable value through technology and human ingenuity.