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Clinical Data Svs Specialist

Accenture
Accenture
7-11 years
Not Disclosed
Bengaluru, Karnataka, India
10 Feb. 24, 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

Job Title: Clinical Data Services Specialist – Clinical EDC Build

Location: Bengaluru, Karnataka, India
Job Type: Full-Time
Experience Level: 7–11 Years
Job Reference: AIOC-S01628461
Qualification: BE / BTech
Company: Accenture

Job Overview

Accenture is hiring a Clinical Data Services Specialist to support its Life Sciences R&D vertical, focusing on Clinical EDC Build and advanced clinical data solutions. This role plays a critical part in the development, configuration, and maintenance of electronic clinical study databases, ensuring high-quality, regulatory-compliant data management across global clinical trials.

The ideal candidate will bring strong expertise in clinical data acquisition, Electronic Data Capture (EDC) systems, Elluminate Clinical Data Cloud, and reporting technologies used in drug development. This position requires both technical proficiency and leadership capability to manage moderately complex deliverables and small teams when required.

About the Organization

Accenture is a global professional services company delivering Strategy, Consulting, Technology, and Operations services across more than 120 countries. Within the Life Sciences R&D vertical, Accenture supports clinical trials, regulatory services, pharmacovigilance, and patient-centered innovation for leading biopharmaceutical organizations worldwide.

Key Responsibilities

  • Develop and configure clinical study databases, including electronic Case Report Forms (eCRFs) and edit checks as per study specifications

  • Support protocol amendments and database updates through structured change control processes

  • Manage clinical data ingestion, transformation pipelines, and data standardization workflows within Elluminate Clinical Data Cloud

  • Enable automation workflows and analytics integration for sponsor reporting requirements

  • Perform analysis and resolution of moderately complex clinical data challenges

  • Leverage and adapt existing methodologies to create optimized data management solutions

  • Collaborate with clinical, regulatory, and analytics stakeholders to ensure high-quality data delivery

  • Support client engagement and maintain strong professional relationships

  • Guide team members and contribute to small team management where applicable

  • Work in rotational shifts if required by project needs

Experience Required

  • 7–11 years of experience in Clinical Data Management or Clinical Data Services

  • Strong background in Life Sciences and clinical trial data processes

  • Hands-on experience in Clinical EDC Build and database configuration

  • Proven expertise in Elluminate Clinical Data Cloud, including data integration and automation workflows

  • Experience with clinical reporting technologies such as Spotfire, Qlik, JReview, Cognos, BOXI, or similar platforms

  • Knowledge of global regulatory compliance standards related to clinical trials

  • Experience supporting clinical drug development programs

Educational Qualification

  • BE / BTech in relevant discipline

  • Strong foundation in clinical data systems and technology platforms

Core Competencies

  • Problem-solving and analytical thinking

  • Ability to perform under pressure and meet strict timelines

  • Adaptability and quick learning agility

  • Strong client relationship management skills

  • Understanding of strategic objectives and alignment with team goals

  • Leadership capability for small teams or workstreams

  • Knowledge of clinical trial lifecycle and regulatory data standards

Why Join Accenture – Life Sciences R&D?

  • Work with global biopharma clients across clinical, pharmacovigilance, and regulatory domains

  • Exposure to advanced clinical data cloud technologies and analytics platforms

  • Opportunity to contribute to end-to-end clinical trial data management

  • Career growth within a globally recognized digital and consulting organization

Accenture is an Equal Opportunity Employer and maintains a commitment to diversity, inclusion, and compliance with global regulatory standards.

This job listing is optimized for search visibility in Clinical Data Services Specialist, Clinical EDC Build Expert, Elluminate Clinical Data Cloud, Clinical Database Development, and Life Sciences R&D Technology careers in India and global markets on ThePharmaDaily.com.