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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:

Burlington, United States (Remote)


Job ID:

2025-118022


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:

About ICON:
ICON plc is the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence and committed to excellence and innovation in clinical development.


Key Responsibilities:

  • Manage clinical trial documents, logistics, and administrative support throughout all trial phases (feasibility to close-out)

  • Ensure adherence to GCP, SOPs, Health Care Compliance (HCC), and local regulations

  • Partner with Local Trial Managers (LTMs) and Site Managers (SMs) to support site-level trial activities

  • Track trial progress, manage study data, investigational products, mailings, and correspondence

  • Maintain protocol information in trial management systems; distribute safety updates

  • Provide investigational sites with up-to-date trial documents and materials

  • Archive and reconcile study files; ensure audit and inspection readiness

  • Review technical regulatory documents, including informed consent forms

  • Prepare study start-up and submission documents for IEC/IRB and health authorities

  • Track and manage financial disclosure documentation

  • Coordinate study file creation and update internal trial document repositories

  • Assist with budget management and vendor invoice reconciliation (if requested)

  • Organize training sessions and investigator meetings when required


Qualifications & Experience:

  • Education:

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

  • Experience:

    • 1–2 years of relevant experience in clinical trials

    • Strong proficiency in MS Office (Word, Excel, Access, Outlook, Explorer, PowerPoint)

    • Strong interpersonal, negotiation, and organizational skills

    • Ability to manage multiple priorities in a matrix environment

    • Experience with VeevaVault TMF preferred

    • Fluent in English (written and spoken)


Salary Range:

Not specified in posting. Compensation will be competitive and based on location, experience, and skill level.


ICON Employee Benefits Include:

  • Annual leave entitlements

  • Multiple health insurance options

  • Competitive retirement savings plans

  • TELUS Health Global Employee Assistance Program

  • Life insurance

  • Optional benefits: gym memberships, bike-to-work programs, travel passes, childcare vouchers, health checks, and more

🔗 Full details: ICON Careers – Benefits


Diversity & Accessibility Statement:

ICON is committed to an inclusive, diverse, and equitable work environment.
🔗
Request reasonable accommodation