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Clinical Data Svs Associate

0-2 years
Not Disclosed
10 Aug. 21, 2025
Job Description
Job Type: Full Time Education: B.E./B.Pharm/M.Pharm 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
Company: Accenture
Job ID: AIOC-S01580142
Job Type: Full-Time | Experience: 0–2 years

About the Company:
Accenture is a global professional services company with expertise in digital, cloud, and security. With 775,000+ employees across 120+ countries, Accenture helps the world’s leading organizations drive transformation across industries. In Life Sciences R&D, Accenture delivers integrated services spanning clinical trials, pharmacovigilance, regulatory solutions, and patient engagement.

Role Overview:
As a Clinical Data Services Associate, you will support data management activities within Accenture’s Life Sciences R&D vertical. You will work with global biopharma clients, ensuring clinical trial data integrity, compliance, and readiness for regulatory submission through SDTM (Study Data Tabulation Model) mapping and related processes.

Key Responsibilities:

  • Perform data management tasks including discrepancy review, query generation, and resolution.

  • Create and maintain CRF Completion Guidelines (CCG) and SAE reconciliation guidelines.

  • Identify and document protocol deviations in trial databases.

  • Conduct edit check validation by designing test cases and scripts.

  • Perform User Acceptance Testing (UAT) of clinical trial databases against CRF/eCRF specifications.

  • Support preparation of datasets (SDTM format) for regulatory submission (e.g., FDA, EMA).

  • Collaborate with internal teams to manage clinical data projects, ensuring accuracy and compliance.

Qualifications:

  • BE, Bachelor of Pharmacy, or Master of Pharmacy (mandatory).

  • 0–2 years of experience (freshers with relevant academic projects welcome).

  • Strong foundation in clinical research processes and medical/pharma terminology.

  • Working knowledge of SDTM mapping preferred.

  • Proficiency in Microsoft Office; knowledge of CDM tools (e.g., Medidata Rave, Oracle Clinical) is an advantage.

Skills & Competencies:

  • Adaptable and flexible in a dynamic project environment.

  • Quick learner with analytical and detail-oriented mindset.

  • Strong team player with effective communication skills.

  • Willingness to work in rotational shifts as required.

Compensation & Benefits:

  • Competitive salary aligned with Accenture’s global standards for entry-level roles (₹4–6.5 LPA market benchmark).

  • Career advancement opportunities with certifications and continuous learning.

  • Holistic well-being support (physical, mental, and financial).

  • Inclusive workplace recognized as one of the World’s Best Workplaces™.

Why Join Accenture?

  • Work with global life sciences leaders on cutting-edge R&D projects.

  • Gain exposure to regulatory compliance and advanced data management frameworks.

  • Be part of a diverse, inclusive culture fostering innovation and continuous learning.

  • Accelerate your career at the intersection of technology and healthcare.