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Associate Clinical Trial Manager

2-5 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:

Associate Clinical Trial Manager


Location:

United States (Remote)


Job ID:

2025-118322


Department:

Clinical Trial Management – ICON Strategic Solutions


Job Type:

Full-Time, Remote


Application Contact:

Name: Brendan Hoey
Options: View other roles or send a message via the application platform


Job Description:

As an Associate Clinical Trial Manager (ACTM), you will play a key role in supporting and leading operational aspects of clinical studies across various phases. Working closely with the Clinical Operations Lead, you will manage assigned study components, vendors, regions, or entire small trials—contributing to trial strategy, execution, timelines, and compliance. This position offers a great career path toward clinical operations leadership within a global organization.


Key Responsibilities:

  • Manage study components or small trials throughout various phases of the trial lifecycle

  • Deputize for the Clinical Operations Lead as needed

  • Draft and review clinical study documents (protocols, ICFs, study plans, etc.)

  • Oversee assigned vendors and CRO activities

  • Participate in EDC/IRT system builds and clinical review of CRFs

  • Assist in site selection, feasibility, and site contract/budget monitoring

  • Support clinical supplies coordination and regulatory/IRB submissions

  • Maintain and report trial metrics, deviations, and insurance documentation

  • Ensure TMF quality checks and document uploads

  • Mentor Clinical Trial Associates (CTAs) when required

  • Ensure GCP and ICH compliance throughout the study lifecycle


Required Qualifications:

  • 2–5 years’ experience in clinical research or industry setting (trial coordination or management)

  • Bachelor’s degree in a science-related field (Advanced degree preferred)

  • Experience with global clinical trial operations

  • Strong project management and organizational skills

  • In-depth understanding of FDA, ICH, and GCP guidelines

  • Excellent written and verbal communication


What ICON Offers:

  • Competitive salary

  • Annual leave entitlements

  • Multiple health insurance options

  • Retirement planning and financial wellness programs

  • Global Employee Assistance (TELUS Health)

  • Life assurance

  • Country-specific flexible perks: gym subsidies, travel passes, childcare vouchers, etc.
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    Explore ICON Benefits


Inclusion & Accessibility:

ICON embraces diversity and strives to ensure an inclusive, accessible hiring experience for all applicants.
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