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Sr Clinical Db Designer

2-4 years
Not Disclosed
10 May 19, 2025
Job Description
Job Type: Full Time Education: B.Tech/BCS/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Sr Clinical DB Designer

Location: Kochi, India
Job Type: Full Time
Job ID: R1473782

Job Overview:
As a Sr Clinical Database Designer at IQVIA, you will be responsible for study build and design, system configurations, and creating edit specifications. You will collaborate with internal and external stakeholders including the Data Team Lead (DTL), programmers, validation teams, vendors, statisticians, and client representatives. Additionally, you will manage project financials related to programming shared services.

Essential Functions:

  • Interpret study protocols to inform database design

  • Design and update eCRFs using third-party or in-house CDMS tools aligned with industry standards (e.g., SDTM, CDASH)

  • Create and maintain Edit Specification Documents

  • Specify EDC build components such as rights and roles, system settings, and homepage configurations

  • Complete Study Authorization Forms and Trial Capacity Request Forms (InForm)

  • Participate in meetings: Pre-Design, Online Screen Review, Unblinded Data Review, and Internal Design Review

  • Lead discussions in Edit Specification Review Meetings and may lead Online Screen Review Meetings

  • Design databases to capture LLRR data within InForm, ensuring proper access rights

  • Identify and escalate project risks or quality concerns to the DTL

  • Ensure timely completion of all project-specific and SOP-mandated training

  • Review timelines and QIPs, identify out-of-scope activities, and inform relevant parties

  • Simultaneously manage multiple study design projects, potentially across different platforms

  • Contribute to ongoing process improvements and participate in improvement initiatives

Qualifications:

  • Education: Bachelor's degree in Science, Computer Science, Information Technology, or equivalent (B.Tech preferred)

  • Experience:

    • 2–4 years of core technical database design experience

    • Total of 7+ years of relevant professional experience

About IQVIA:
IQVIA is a global leader in advanced analytics, technology solutions, and contract research services for the life sciences industry. We build intelligent connections that accelerate innovation, improve healthcare delivery, and enhance patient outcomes. Learn more at
IQVIA Careers