Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Trial Delivery Manager (Tdm)

3-5 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:

Trial Delivery Manager (TDM) – Home Based – Canada


Location:

Remote – Canada


Job ID:

2025-118430


Department:

Clinical Trial Management – ICON Strategic Solutions


Job Type:

Full-Time, Remote


Application Contact:

Name: Brandon Pupek
Options: View other roles or send a direct message through the platform


Job Description:

As a Trial Delivery Manager (Clinical Trial Manager), you will play a leading role in the planning, coordination, and execution of global Phase I–IV clinical trials across multiple therapeutic areas. You will be embedded with a major pharmaceutical client and serve as the Study Management Team leader responsible for delivering high-quality trials within timelines and budget, ensuring compliance with global regulatory and SOP requirements.


Key Responsibilities:

  • Lead global/regional clinical trials from study setup to close-out

  • Oversee study design, team training, and third-party vendor management

  • Track timelines, quality metrics, and budgets; escalate and resolve issues

  • Manage site enrolment and ensure regulatory documentation is updated

  • Support audit and inspection readiness

  • Collaborate with cross-functional and virtual teams globally

  • Drive process improvement and ensure study integrity


Requirements:

  • Education:

    • Bachelor’s degree in Life Sciences (e.g., Biology, Chemistry, Nursing, Pharmacy, Biochemistry)

  • Experience:

    • 3–5 years of clinical trial management experience in CRO or pharma

    • End-to-end global trial management experience (Start-Up to Database Lock)

    • Strong experience coordinating global/remote teams

    • Experience with oncology, immunology, cardiology/metabolism, infectious diseases, or vaccines is preferred

  • Skills:

    • Proven leadership, organizational, and financial acumen

    • Effective communicator with a proactive risk-management mindset

    • Comfortable working in a virtual team setup

  • Other:

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

    • Willingness to travel up to 20%


Benefits:

  • Competitive salary and comprehensive leave entitlements

  • Health insurance tailored to personal and family needs

  • Retirement planning programs

  • Global Employee Assistance via TELUS Health

  • Life assurance

  • Flexible, country-specific optional benefits:

    • Childcare vouchers, gym discounts, bike schemes, travel subsidies, wellness checks
      🔗
      Explore ICON Benefits


Inclusion & Accessibility:

ICON is committed to providing a diverse, inclusive, and accessible workplace for all. Reasonable accommodations are available for applicants as needed.
🔗
Request accommodations here