Instagram
youtube
Facebook

Clinical Data Svs Associate

0-2 years
Not Disclosed
10 Dec. 2, 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

Clinical Data Services Associate – Accenture | Bengaluru, India

Job ID: AIOC-S01614645
Location: Bengaluru, India
Position: Clinical Data Services Associate
Employment Type: Full Time
Experience Required: 0 to 2 years (Entry-Level to Junior)

Accenture is seeking a Clinical Data Services Associate to support clinical data management and medical monitoring activities within its global Life Sciences R&D operations. This role is designed for early-career professionals aiming to build expertise in clinical data services, data quality oversight, and clinical trial data processes.


About Accenture

Accenture is a global leader in professional services, delivering expertise across digital, cloud, technology, consulting, and operations. With advanced capabilities across more than 40 industries and a global workforce of over 699,000 professionals, Accenture partners with leading organizations to drive innovation and operational excellence. The company operates in more than 120 countries with one of the world’s largest networks of Intelligent Operations Centers.


Role Overview

As a Clinical Data Services Associate, you will support clinical data management activities throughout the clinical trial lifecycle. You will contribute to data review, query management, database validation, and protocol compliance, ensuring high-quality, reliable clinical data for regulatory and scientific decision-making.


Key Responsibilities

  • Support collection, integration, and validation of clinical trial data.

  • Perform discrepancy review, query generation, and query resolution in compliance with project guidelines.

  • Assist in development of CRF Completion Guidelines (CCG) and SAE Reconciliation Guidelines.

  • Identify and document protocol deviations in the clinical database.

  • Execute edit check validation by creating test scripts and test cases.

  • Conduct database validation (UAT) as per CRF/eCRF specifications.

  • Contribute to clinical data management project activities and timelines.

  • Provide medical input for trial oversight and safety considerations based on protocol requirements.

  • Collaborate with team members, following established instructions and standard operating procedures.

  • Work within defined job scope as an individual contributor.

  • Be prepared to work in rotational shifts as needed.


Required Experience

  • 0 to 2 years of experience in Clinical Data Management, Clinical Research, Pharmacovigilance, or Life Sciences operations.

  • Fresh graduates with strong analytical and data-oriented skills are encouraged to apply.


Educational Qualifications

Candidates must hold one of the following degrees:

  • Bachelor of Engineering (BE)

  • Bachelor of Pharmacy (B.Pharm)

  • Master of Pharmacy (M.Pharm)


Key Skills and Competencies

  • Analytical and problem-solving skills

  • Strong written and verbal communication

  • Adaptability and flexibility in dynamic project environments

  • Understanding of clinical data processes and documentation standards

  • Ability to work effectively within cross-functional teams