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Global Clinical Trial Associate - Medical Affairs

1-2 years
Not Disclosed
10 April 18, 2025
Job Description
Job Type: Full Time Remote 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:

Global Clinical Trial Associate – Medical Affairs


Location:

Canada (Remote / Home-Based)


Job ID:

2025-118018


Department:

Clinical Trial Support – ICON Strategic Solutions


Job Type:

Full-Time, Remote


Application Contact:

Name: Jamie Pruitt
Options: View other roles or send a direct message through the platform


Job Description:

As a Clinical Trial Associate, you’ll be an integral part of the world’s largest and most comprehensive clinical research organization. You'll manage essential documentation and administrative tasks throughout the trial lifecycle—covering feasibility, initiation, execution, and close-out phases.


Key Responsibilities:

  • Maintain regulatory compliance (GCP, GCO SOPs, HCC, local regulations)

  • Support LTMs and SMs with overall site management

  • Review technical and regulatory documents, including ICFs

  • Manage data tracking, budgets, correspondence, investigational products, and mailings

  • Ensure current versions of trial documents and materials are distributed to sites on time

  • Handle filing and archiving of documents and ensure audit/inspection readiness

  • Support financial documentation and invoice reconciliation (if requested)

  • Track investigator documentation, site feasibility, and financial disclosure information

  • Prepare internal data repositories and ensure document completeness

  • Coordinate SM/SIV training sessions (if applicable)

  • Participate in process improvements


Requirements:

  • Education:

    • BA/BS in Life Sciences, Nursing, or related field (or equivalent work experience)

  • Experience:

    • 1–2 years in clinical trial roles with relevant skills

    • Proficient in English (spoken & written)

    • Strong command of MS Office suite (Word, Excel, Access, Outlook, Explorer, PowerPoint)

    • Familiarity with VeevaVault TMF is desirable

    • Excellent organizational, interpersonal, and negotiation skills

    • Capable of working under multiple priorities in a matrix setup


Benefits:

  • Competitive salary

  • Comprehensive health insurance packages

  • Retirement planning support

  • Flexible annual leave options

  • Access to TELUS Health’s 24/7 global wellness network

  • Life assurance and country-specific optional benefits (e.g., gym, bike programs, travel subsidies)
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    Full benefits information


Inclusion & Accessibility:

ICON is committed to fostering an inclusive workplace where every individual is respected and supported.
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Request reasonable accommodations