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Investigator Payments Analyst

2+ years
Not Disclosed
10 April 7, 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 Title: Contract Specialist – Clinical Trial Start-Up

Company: IQVIA
Department: Regulatory & Start-Up (RSU)
Location: Not specified
Job Type: Full-Time


Job Overview

Support the delivery of all required start-up contracting activities for selected sponsors, studies, or multi-protocol programs, including pre-award activities, per agreed sponsor requirements or internal algorithms.


Essential Functions

  • Develop basic investigator grant estimates and proposal text to aid in proposal development.

  • Use and maintain contract and budget templates, systems, and tools according to project scope and plans.

  • Collaborate with sponsors, stakeholders, and RSU teams to ensure project success and compliance.

  • Provide operational and financial support to ensure trial efficiency and regulatory compliance.

  • Create/review core documentation to support business development and study maintenance.

  • Analyze and distribute contracting intelligence for assigned studies and broader company use.

  • Track and report contracting efficiency, performance metrics, and out-of-scope activities.

  • Ensure contract management quality standards and support RSU team as needed.

  • Maintain internal systems including CTMS, databases, tracking tools, and project plans.


Qualifications

  • Education: Bachelor’s Degree (required)

  • Experience: Minimum 1 year relevant experience, especially in contract negotiation

  • Skills & Knowledge:

    • Strong negotiation and communication abilities

    • Technical writing proficiency

    • Understanding of GCP/ICH guidelines and clinical trial regulations

    • Familiarity with drug development and clinical trial environments

    • Knowledge of SOPs and corporate standards

    • Proficient in Microsoft Office and email systems

    • Ability to interpret pricing models and prepare proposals/budgets

    • Strong organizational and planning skills

    • Effective team collaboration within a matrix environment


About the Company

IQVIA is a global leader in clinical research, commercial insights, and healthcare intelligence. The company accelerates innovation and improves healthcare outcomes through intelligent connections in data, technology, and expertise.