Instagram
youtube
Facebook

Clinical Db Designer

0-2 years
Not Disclosed
10 April 8, 2025
Job Description
Job Type: Full Time Education: 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

Job profile: Clinical DB Designer

Company: IQVIA

Location: Kochi, India

Job Type: Full-time

Job ID: R1473826


Job Overview:

The Clinical Database Designer is responsible for study design, creation of edit specifications, and system configurations for electronic data capture (EDC). Accountable for quality and timely delivery of assigned design components in collaboration with project stakeholders.


Key Responsibilities:

Study Design & Specification:

  • Interpret study protocols for design implementation

  • Design and update electronic Case Report Forms (eCRFs)

  • Create and maintain Edit Specification Documents

  • Generate specifications for various EDC build components such as:

    • Rights and Roles

    • System Settings

    • Study Home Page

Documentation & Authorization:

  • Complete Study Authorization Form and Trial Capacity Request Form (specific to InForm platform)

Meetings & Reviews:

  • Attend project meetings such as:

    • Pre-Design Meeting

    • Online Screen Review Meeting

    • Unblinded Data Review Meeting

    • Internal Design Review Meeting

  • Facilitate internal Edit Specification Review Meetings and lead discussions

Database Configuration:

  • Design databases to support LLRR (Last Log Review Report) data collection in the InForm system

  • Ensure appropriate access rights are documented for data entry and update through the Rights and Roles configuration


Qualifications:

  • No specific qualifications were listed in this job description, but typical expectations include:

    • Bachelor’s degree in Life Sciences, Computer Science, or related field (preferred)

    • Experience with clinical trial database platforms (e.g., InForm, RAVE)


Key Skills:

  • Clinical trial protocol interpretation

  • eCRF design and edit specification development

  • EDC platform configuration (especially InForm)

  • Effective documentation and review facilitation

  • Collaborative and detail-oriented work approach


About IQVIA:

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services. Their mission is to use data science and human science to help healthcare clients improve patient outcomes and accelerate medical innovation.
🔗
Learn more