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Clinical Data Svs Associate

0-2 years
Not Disclosed
10 May 16, 2025
Job Description
Job Type: Full Time Education: BE/BTech/BCA 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 Associate
Experience: 1–3 Years
Job Type: Full Time
Location: Bengaluru
Job Code: AIOC-S01575283


About the Company:
Accenture is a global professional services firm with advanced capabilities in digital, cloud, and security. Serving clients in over 120 countries, Accenture brings unmatched expertise across more than 40 industries, offering Strategy and Consulting, Technology, Operations, and Accenture Song. With a workforce of over 775,000 professionals, the company is driven by a shared purpose—to harness the power of change and deliver long-lasting value to clients, communities, and society. Learn more at
www.accenture.com.


Key Skills Required:

  • Oracle Procedural Language Extensions to SQL (PL/SQL)

  • Structured Query Language (SQL)

  • Clinical SAS Programming

  • Clinical Database Programming

  • Clinical Data Management

  • Adaptability and Flexibility

  • Problem-Solving Skills

  • Ability to Perform Under Pressure

  • Client Relationship Management

  • Quick Learning Agility


Qualifications:

  • BE

  • BTech

  • BCA


Years of Experience:

  • 1 to 3 years


Roles and Responsibilities:

  • Solve routine clinical database programming tasks using established guidelines

  • Develop and review complex clinical trial reports, including patient profile listings and preprocessing checks

  • Utilize tools such as Cognos, SAS, and J-Review for validation and data mapping

  • Write programs in PL/SQL, SQL, and Clinical SAS for integrating data from multiple sources (e.g., EDC, Labs, IRT)

  • Maintain report compliance with regulatory standards

  • Implement strict quality control for data accuracy and report integrity

  • Collaborate with clinical operations, biostatistics, and other departments to ensure stakeholder requirements are met

  • Follow detailed instructions for new assignments with moderate supervision for routine tasks

  • Act as an individual contributor within a predefined scope of work

  • Role may require working in rotational shifts


Additional Information:

  • Accenture is an Equal Opportunity Employer

  • Employment decisions are made without discrimination based on age, gender, race, disability, or any other protected status under applicable law

  • Accenture promotes a culture of inclusivity, professional development, and holistic well-being