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Clinical Data Svs Associate

Accenture
Accenture
1-3 years
Not Disclosed
10 Dec. 31, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Data Services Associate

Location: Bengaluru, India
Job Type: Full-Time
Experience Required: 1–3 Years
Functional Area: Clinical Data Management / Life Sciences


Company Overview

Accenture is a global professional services company delivering unmatched capabilities in digital, cloud, and security. Serving clients across 40+ industries, we combine strategy, consulting, technology, and operations expertise to drive transformation. With a workforce of 699,000 professionals worldwide, we empower organizations to achieve innovation and operational excellence.


Role Overview

We are seeking a Clinical Data Services Associate to support the Life Sciences R&D vertical. The role involves clinical trial data management, validation, and analysis, ensuring data accuracy, integrity, and regulatory compliance. This position is ideal for BE, B.Pharm, or M.Pharm graduates seeking hands-on experience in clinical research and data-driven decision-making.


Key Responsibilities

  • Manage and process data collected during clinical trials, ensuring accuracy and reliability for analysis.

  • Provide medical expertise for trial oversight and safety concerns.

  • Support creation, review, and validation of protocol requirement specifications in line with applicable SOPs.

  • Solve routine data management issues following guidelines and standard practices.

  • Collaborate with team members and direct supervisors to ensure seamless workflow.

  • Work as an individual contributor with a focused scope of tasks while maintaining high-quality standards.

  • May require participation in rotational shifts to support global clinical trials.


Qualifications & Experience

  • Education: BE, B.Pharm, or M.Pharm.

  • Experience: 1–3 years in clinical data management or related areas.

  • Strong analytical, problem-solving, and data handling skills.

  • Ability to work independently and collaboratively within a team.

  • Adaptable and flexible to changing priorities and requirements.


Why Join Accenture

  • Gain exposure to clinical trial data management and medical monitoring across life sciences projects.

  • Work with global clients and cross-functional teams to support regulatory-compliant trial outcomes.

  • Access to continuous learning, certifications, and career growth opportunities.

  • Be part of a diverse, inclusive, and innovative work environment.


Equal Opportunity Employer

Accenture is committed to providing equal employment opportunities. We do not discriminate based on age, race, religion, gender, disability, or any other legally protected status.