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Clinical Data Svs Associate

Accenture
Accenture
1-3 years
preferred by company
10 Jan. 26, 2026
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 – Life Sciences R&D

Job ID: AIOC-S01623599
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Experience Required: 1–3 years
Function: Clinical Data Services | Medical Monitoring


About Accenture

Accenture is a global professional services leader with deep expertise across digital, cloud, security, and intelligent operations. With a workforce of over 780,000 professionals serving clients in more than 120 countries, Accenture partners with organizations across industries to drive innovation and deliver measurable value. Within the Life Sciences R&D vertical, Accenture supports leading biopharmaceutical companies across clinical trials, pharmacovigilance, regulatory services, and patient-focused solutions.


Job Overview

The Clinical Data Services Associate will support clinical data management and medical monitoring activities within Accenture’s Life Sciences R&D operations. This role focuses on the collection, validation, processing, and oversight of clinical trial data to ensure accuracy, regulatory compliance, and data integrity. The position is well-suited for early-career professionals seeking exposure to global clinical research and data-driven trial operations.


Key Responsibilities

  • Support clinical data services activities, including data collection, validation, storage, and review across clinical trials

  • Assist in ensuring clinical trial data accuracy, consistency, and compliance with applicable SOPs and regulatory standards

  • Provide medical and protocol-related support for trial oversight and safety considerations

  • Contribute to the creation, review, and validation of protocol requirement specifications

  • Follow established guidelines and standard procedures to resolve routine operational issues

  • Collaborate primarily with immediate team members and direct supervisors

  • Execute assigned tasks based on detailed to moderate work instructions

  • Operate as an individual contributor within a structured team environment

  • Support operational requirements, including working in rotational shifts when required


Required Qualifications & Experience

  • Education: BE / BCA / Bachelor of Pharmacy (B.Pharm)

  • Experience Required: 1–3 years of experience in clinical data services, clinical data management, or related life sciences roles


Required Skills & Competencies

  • Basic understanding of clinical trial data management and medical monitoring processes

  • Ability to work effectively within defined procedures and regulatory frameworks

  • Adaptability and flexibility in a dynamic operational environment

  • Strong learning agility and willingness to acquire new technical and domain skills

  • Attention to detail and commitment to data accuracy and quality

  • Ability to work collaboratively as part of a team

  • Good communication and organizational skills


Why Join Accenture

  • Opportunity to work with leading global biopharmaceutical and life sciences organizations

  • Exposure to end-to-end clinical research and data operations

  • Structured training and career development pathways

  • Inclusive, diverse, and performance-driven work culture

  • Chance to contribute to high-impact healthcare and clinical research initiatives


Apply now on thepharmadaily.com to begin or advance your career in Clinical Data Services and Medical Monitoring with Accenture.