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Global Clinical Trial Associate - Medical Affairs

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ICON
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:

Burlington, United States (Remote)


Job ID:

2025-118020


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 Global Clinical Trial Associate, you will manage the logistics, documents, and administrative tasks associated with clinical trials. This includes supporting trial feasibility, startup, execution, and close-out. You will ensure compliance with GCP, SOPs, and local regulations while assisting with protocol-related activities.


Key Responsibilities:

  • Manage trial documents, budgets, investigational products, and communications

  • Ensure compliance with GCP, local regulations, and applicable SOPs

  • Track study progress and assist with start-up/submission to relevant boards

  • Coordinate document collection and filing for study milestones

  • Ensure audit and inspection readiness

  • Provide process improvement suggestions and manage trial-related materials

  • Track financial disclosures and study budgets as needed

  • Support Site Managers (SM) and Trial Managers (TM) in various administrative tasks


Requirements:

  • Education:

    • BA/BS degree in Life Sciences, Nursing, or related scientific field, or equivalent experience

  • Experience:

    • 1-2 years of relevant clinical trial experience

    • Familiarity with MS Office (Word, Excel, PowerPoint)

    • Experience with VeevaVault TMF is desirable

    • Strong interpersonal and organizational skills

    • Proficiency in spoken and written English

    • Ability to work in a matrix environment and handle multiple priorities

  • Eligibility:

    • Legally authorized to work in the United States without requiring future sponsorship


Benefits:

  • Competitive salary and annual leave

  • Health insurance options for you and your family

  • Retirement planning with strong savings benefits

  • Global Employee Assistance Program (TELUS Health)

  • Life assurance

  • Country-specific optional benefits (childcare vouchers, gym memberships, etc.)
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    Explore ICON Benefits


Inclusion & Accessibility:

ICON is committed to an inclusive and accessible environment for all candidates, ensuring equal consideration for employment.
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