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Clinical Data Svs Specialist

Accenture
Accenture
7-11 years
Not Disclosed
10 Jan. 6, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 Specialist – Bengaluru, India (Full-time)

Experience Required: 5–10 Years | Job ID: AIOC-S01619734 | Location: Bengaluru, Karnataka | Industry: Life Sciences & Healthcare

Accenture is seeking a highly skilled Clinical Data Services Specialist to join its Life Sciences R&D vertical in Bengaluru. This role is ideal for professionals with strong expertise in clinical data management, clinical trial reporting, and regulatory compliance, who are looking to work in a global professional services environment.


About the Role

As a Clinical Data Services Specialist, you will support the management and processing of clinical trial data, ensuring accuracy, reliability, and compliance with regulatory standards. You will work on designing, building, and analyzing clinical databases and generating clinical trial reports using tools such as SAS, J-Review, Cognos, SQL, and PL/SQL. This role also offers the opportunity to lead small teams, contribute to project strategy, and work closely with clients in the biopharma and life sciences domain.


Key Responsibilities

  • Manage, validate, and analyze clinical trial data to ensure integrity and compliance.

  • Design and develop Clinical EDC systems, including database programming and build.

  • Develop, validate, and generate clinical trial reports using SAS, J-Review, Cognos, SQL, and PL/SQL.

  • Apply analytical skills to solve moderately complex problems and create solutions leveraging existing methods and procedures.

  • Collaborate with internal teams, clients, and management to align deliverables with strategic goals.

  • Lead small teams or project work efforts, providing guidance on new assignments and methodologies.

  • Participate in rotational shifts as required by project needs.


Required Qualifications & Skills

  • Bachelor’s degree in Engineering (BE/BTech).

  • 5–10 years of experience in clinical data management, clinical trial reporting, or life sciences data analysis.

  • Proficiency in clinical database programming, SQL, SAS, J-Review, Cognos, and PL/SQL.

  • Experience in Clinical EDC design and build.

  • Strong analytical, problem-solving, and communication skills.

  • Ability to manage small teams or work independently on client projects.


Preferred Experience

  • Exposure to clinical trials, pharmacovigilance, or regulatory data services.

  • Familiarity with global life sciences R&D processes and US/European regulatory requirements.


Working Hours & Location

  • Location: Bengaluru, Karnataka, India

  • Working Mode: Full-time, may require rotational shifts


Why Join Accenture?

Accenture is a global leader in digital, cloud, and security services, with a presence in over 120 countries. We offer professionals the opportunity to work on high-impact projects, develop new skills, and contribute to transformative solutions in life sciences and healthcare. We embrace diversity and inclusion, supporting a workplace free from bias and fostering professional growth.

Equal Opportunity Employer: All employment decisions at Accenture are made without regard to age, race, religion, sex, disability, or any other legally protected status.

Learn more: www.accenture.com