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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:

2025-117722


Department:

Clinical Trial Support – ICON Strategic Solutions


Job Type:

Full-Time, Remote


Application Contact:

Name: Jamie Pruitt
Message Option: Available via the job platform
View Roles: See Jamie’s other open roles


Job Description:

As a Clinical Trial Associate, you will be joining the world’s largest and most comprehensive clinical research organization, delivering critical support throughout the clinical trial lifecycle under the Medical Affairs division.


Key Responsibilities:

  • Manage documents, logistics, and administrative tasks related to feasibility, start-up, execution, and close-out of clinical trials

  • Ensure compliance with GCP, HCC, SOPs, and regulatory requirements

  • Review regulatory documents (e.g., Informed Consent Forms) and track site-level trial activities

  • Collaborate with Local Trial Managers (LTMs) and Site Managers (SMs) on site management

  • Maintain accurate trial information in management systems and ensure timely document submission

  • Prepare and archive study documentation and ensure audit/inspection readiness

  • Support financial documentation, invoice reconciliation, and vendor liaison as needed

  • Manage correspondence, updates to internal data repositories, and study file completeness

  • Assist with training coordination for SIVs or investigator meetings (if requested)

  • Participate in process improvement initiatives

  • Handle site contracting, financial disclosures, and ethics/regulatory submissions


Qualifications & Experience:

  • Education:

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

  • Experience & Skills:

    • 1–2 years of clinical trial experience

    • Proficient in English (spoken and written)

    • Strong Microsoft Office skills (Word, Excel, Access, Outlook, Explorer, PowerPoint)

    • Effective organizational, interpersonal, and negotiation skills

    • Experience working in a matrix environment with multiple priorities

    • Familiarity with VeevaVault TMF is desirable


Benefits Offered by ICON:

  • Competitive salary and global health insurance options

  • Retirement savings plans

  • Annual leave entitlements

  • Flexible, country-specific optional benefits (e.g., gym discounts, travel passes)

  • Life assurance

  • Employee Assistance Program via TELUS Health (24/7 support access) 🔗 ICON Careers – Benefits


Diversity & Accessibility Statement:

ICON fosters a culture of inclusion and belonging, offering an accessible and non-discriminatory environment for all candidates.
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