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Clinical Data Svs Associate

0-2 years
Not Disclosed
10 Sept. 16, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ 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 – SDTM Mapping

Skill Required: Clinical Data Services – SDTM Mapping

Designation: Clinical Data Services Associate

Qualifications:

  • B.E. / Bachelor of Pharmacy / Master of Pharmacy

Experience:

  • 1 to 3 years


About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song—all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers.

Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners, and communities.
Visit us at www.accenture.com.


About the Role

You will be aligned with the Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, including:

  • Research laboratories

  • Clinical trials support

  • Regulatory services

  • Pharmacovigilance and patient services

Within this span, you will be part of Clinical, Pharmacovigilance & Regulatory Services, helping leading biopharma companies bring their vision to life by improving outcomes through patient-centric solutions.

The Clinical Data Management team focuses on:

  • Collection, integration, and availability of clinical trial data at appropriate quality and cost

  • Performing data management activities such as discrepancy review, query generation, and resolution

  • Creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines

  • Identifying and raising protocol deviations in the database

  • Conducting edit check validation (test case creation, test scripts, and UAT against CRF/eCRF)

  • Managing clinical data management projects

  • Supporting standard structures for clinical and non-clinical study data tabulations required for regulatory submissions (e.g., FDA).


What We Are Looking For

  • Adaptability and flexibility

  • Agility for quick learning


Roles and Responsibilities

  • Solve routine problems by referring to precedents and general guidelines

  • Work closely with your own team and direct supervisor

  • Follow detailed to moderately detailed instructions for daily tasks; receive detailed guidance on new assignments

  • Make decisions that primarily impact your own work

  • Contribute as an individual team member with a focused scope of responsibilities

  • Be open to working in rotational shifts, if required