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Trial Delivery Manager (Tdm) Advanced

6-8 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:

Trial Delivery Manager (TDM) – Advanced


Location:

Remote – United States or Canada (East Coast Preferred)


Job ID:

2025-118740


Department:

Clinical Trial Management – ICON Strategic Solutions


Job Type:

Full-Time, Remote


Application Contact:

Name: Brandon Pupek
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Job Description:

As a Senior Global Clinical Project Manager (TDM – Advanced), you will lead the full lifecycle management of Phase I-IV clinical trials across multiple therapeutic areas for a globally recognized pharmaceutical client. You’ll coordinate globally distributed study teams, oversee vendor performance, and ensure regulatory compliance, timeline adherence, and budget control.


Key Responsibilities:

  • Manage the setup, planning, coordination, and closeout of global clinical trials

  • Lead the Study Management Team and maintain ownership of trial execution

  • Track study milestones, manage risks, and escalate issues proactively

  • Ensure documentation accuracy and trial audit-readiness

  • Oversee vendor performance, budget forecasting, and enrolment targets

  • Participate in inspections, internal audits, and quality reviews

  • Deliver protocol-specific training and support continuous improvement

  • Act as liaison between Quality Management and the study team


Requirements:

  • Education:

    • BS or equivalent in Life Sciences (Biology, Chemistry, Biochemistry, Nursing, Pharmacy, etc.)

  • Experience:

    • 6–8 years of experience in clinical trial/project management within CRO or pharmaceutical industry

    • Proven success managing global trials from startup to closeout

    • Minimum of 3 years managing global/regional virtual teams

    • Experience across multiple therapeutic areas (e.g., oncology, cardiology/metabolism, infectious diseases, immunology, vaccines)

  • Skills:

    • Strong project planning and financial management skills

    • Effective leadership in virtual team environments

    • Ability to travel up to 20%

    • Must be authorized to work in the U.S. or Canada without visa sponsorship


Benefits:

  • Competitive salary and generous annual leave

  • Comprehensive health insurance options

  • Retirement and financial planning tools

  • 24/7 Global Employee Assistance Program (TELUS Health)

  • Life assurance

  • Optional benefits (country-specific):

    • Childcare vouchers, bike-to-work schemes, gym discounts, subsidized travel, and health assessments
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Inclusion & Accessibility:

ICON embraces diversity and is committed to providing an inclusive and accessible work environment.
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