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Clinical Data Svs Associate Clinical Data Services Associate

Accenture
Accenture
1-3 years
Not Disclosed
Mumbai, India
10 April 13, 2026
Job Description
Job Type: Full Time Education: M.Sc 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 – Clinical Data Management Jobs Mumbai

Company: Accenture
Location: Mumbai
Job Type: Full-Time
Work Mode: On-site
Experience: 0–2 Years (1–3 Years preferred)
Qualification: MSc (Life Sciences or related field)


Job Overview

The Clinical Data Services Associate role is an entry-level opportunity within Clinical Data Management (CDM), focused on handling and processing clinical trial data to support drug development and regulatory compliance.

This position plays a critical role in ensuring high-quality, accurate, and reliable clinical data, which is essential for evaluating the safety and efficacy of pharmaceutical products. The role is ideal for candidates looking to build a career in clinical research, pharmacovigilance, and regulatory data operations.


Key Responsibilities

Clinical Data Management

  • Manage and process clinical trial data including collection, validation, and storage

  • Perform data cleaning, discrepancy management, and query resolution

  • Ensure data accuracy and consistency across clinical databases

Data Quality & Compliance

  • Ensure adherence to ICH-GCP guidelines and regulatory standards

  • Support data validation and audit readiness activities

  • Maintain high-quality standards for clinical datasets

Clinical Trial Support

  • Assist in data integration and analysis for clinical studies

  • Collaborate with cross-functional teams in clinical operations and data management

  • Support timely delivery of clinical trial milestones

Technical & System Support

  • Utilize clinical data management systems (CDMS/EDC tools)

  • Support lab data management and processing workflows

  • Ensure proper documentation and tracking of clinical data activities


Required Skills & Qualifications

Education

  • MSc in:

    • Life Sciences

    • Clinical Research

    • Biotechnology

    • Pharmacy or related field

Experience

  • 0–2 years of experience in:

    • Clinical Data Management

    • Clinical Research

    • Healthcare data operations

Technical & Industry Skills

  • Basic knowledge of:

    • Clinical Data Management (CDM) processes

    • ICH-GCP guidelines

    • Clinical trial lifecycle

  • Familiarity with:

    • EDC/CDMS systems

    • Data validation and query management

Core Competencies

  • Strong attention to detail

  • Problem-solving and analytical thinking

  • Ability to work under pressure in fast-paced environments

  • Strong communication and stakeholder interaction skills

  • Adaptability and flexibility


Perks & Benefits

  • Opportunity to work with a global leader in healthcare and technology consulting

  • Exposure to end-to-end clinical trial data management processes

  • Career growth in clinical research, pharmacovigilance, and regulatory domains

  • Access to learning programs, certifications, and skill development

  • Inclusive and collaborative work environment


About the Company

Accenture is a global professional services company specializing in digital, cloud, and healthcare solutions. With operations in over 120 countries, Accenture supports pharmaceutical and life sciences organizations in clinical research, regulatory compliance, and data-driven innovation.


Salary / Compensation

💰 Not disclosed in the job description (Competitive as per industry standards)


Work Mode

📍 On-site – Mumbai, India


How to Apply

Interested candidates should apply with an updated CV highlighting:

  • Knowledge of clinical data management and clinical trials

  • Experience with EDC/CDMS tools or healthcare data systems

  • Understanding of GCP and regulatory compliance frameworks


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