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Irt Validator

0-2 years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Remote 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: IRT Validator
Location: Navi Mumbai, India
Department: Data Management
Job ID: 10845

Job Summary:

Medpace is seeking a full-time, office-based IRT Validator to join our Randomization and Study Product Management team in Mumbai, India. This role is pivotal in the clinical trial management process, ensuring the quality and accuracy of clinical data related to randomization and study product management. If you have expertise in validation and want to grow your career in clinical trials, this is the perfect opportunity!

Responsibilities:

  • Test Plan Creation: Develop test plans for new projects and system changes.
  • Execution of Test Plans: Implement test plans and create validation packages.
  • Review of Validation Packages: Assess validation packages created by other team members.
  • Document Review: Evaluate requirement specification documents provided by internal clients.
  • Validation of Projects: Validate new projects and modifications to existing projects.

Qualifications:

  • Education: Bachelor’s degree in Math, Computer Science, or a related field.
  • Skills & Experience:
    • Proven ability to complete validation tasks within defined timelines and quality standards.
    • Fluent in English.

Medpace Overview:

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the development of safe and effective therapeutics globally. With 5,000+ employees across 40+ countries, we leverage local regulatory and therapeutic expertise to deliver excellence in clinical trials across a range of therapeutic areas.

Why Medpace?

  • People. Purpose. Passion: Join a passionate team committed to improving global healthcare.
  • Perks:
    • Flexible work environment
    • Competitive compensation and benefits
    • Generous PTO
    • Opportunities for professional growth and career advancement
    • Employee appreciation events and health & wellness initiatives

Are you ready to make an impact on the future of clinical trials? Apply now to be part of Medpace!