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Clinical Data Svs Specialist

Accenture
Accenture
7-11 years
preferred by company
10 Jan. 20, 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
Job ID: AIOC-S01619734
Location: Bengaluru, Karnataka, India
Job Type: Full-Time
Experience Required: 7–11 Years
Industry: Clinical Data Management | Clinical Reporting | Life Sciences R&D


About Accenture

Accenture is a global professional services leader with strong capabilities in digital, cloud, and security. With expertise spanning more than 40 industries, Accenture delivers Strategy & Consulting, Technology, Operations, and Accenture Song services through its global network of Advanced Technology and Intelligent Operations centers. Accenture partners with leading life sciences organizations to accelerate clinical development and deliver patient-centric innovation.


Job Overview

Accenture is seeking an experienced Clinical Data Services Specialist to support advanced clinical data services and clinical reports management within its Life Sciences R&D vertical. This senior role focuses on clinical database programming, EDC design and build, and development of high-quality clinical trial reports using industry-standard tools. The position may involve team leadership responsibilities and collaboration with global stakeholders.


Key Responsibilities

  • Develop and deliver clinical trial reports using tools such as SAS, J-Review, Cognos, SQL, and PL/SQL based on study requirements

  • Support clinical data services including data validation, reporting, and analysis for global clinical trials

  • Design, build, and support Clinical EDC systems, including EDC design and database programming

  • Manage and resolve moderately complex data and reporting challenges, proposing innovative and efficient solutions

  • Align deliverables with strategic goals defined by senior management

  • Collaborate with internal teams, client stakeholders, and cross-functional partners

  • Provide guidance on methodologies and procedures for new assignments

  • Manage small teams or workstreams, or act as a senior individual contributor as required

  • Ensure compliance with regulatory standards, SOPs, and quality guidelines

  • Support operations that may require working in rotational shifts


Required Skills & Experience

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

  • Strong expertise in clinical database programming and EDC build/design

  • Hands-on experience with SAS, J-Review, Cognos, SQL, and PL/SQL

  • Solid understanding of clinical trial data standards and regulatory requirements

  • Proven ability to analyze and solve moderately complex technical and data-related problems

  • Experience leading small teams or managing workstreams is preferred


Educational Qualifications

  • BE / BTech (mandatory)


Role Characteristics

  • Senior-level role with responsibility for project delivery and quality outcomes

  • Ability to influence team deliverables and contribute to strategic objectives

  • Regular interaction with supervisors, peers, and client stakeholders


Why Join Accenture?

  • Work with global biopharmaceutical clients on high-impact clinical research programs

  • Exposure to advanced clinical data platforms and reporting technologies

  • Clear career growth pathways within Life Sciences R&D and data leadership roles


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