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Clinical Trial Liaison

2+ years
Not Disclosed
10 April 24, 2025
Job Description
Job Type: Full Time Education: MD/PhD/PharmD 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: Clinical Trial Liaison

Location: Vancouver, BC (Hybrid: Office/Remote)

About ICON plc:
ICON plc is a leading global healthcare intelligence and clinical research organization. We are committed to driving innovation through our inclusive culture. Join us in shaping the future of clinical development.

Role Summary:
ICON is seeking a Clinical Trial Liaison (CTL) to join our field-based team. In this role, you will serve as a scientific and clinical support specialist for study sites, driving successful trial execution by ensuring sites have a thorough understanding of study design and procedures. You will collaborate cross-functionally to implement recruitment strategies and facilitate patient enrollment. This is a field-based position, requiring the ability to engage with site staff, investigators, and stakeholders at industry meetings and conferences.

Key Responsibilities:

  • Serve as the primary scientific and clinical contact for study sites, providing support to investigators and staff.

  • Develop and optimize strategies to drive patient enrollment and support recruitment efforts.

  • Provide on-site and remote assistance to ensure site compliance with study design and protocols.

  • Collaborate with cross-functional teams to execute operational and strategic goals.

  • Cultivate strong relationships with stakeholders, including medical and scientific leaders, to drive trial success.

  • Represent ICON in industry events and conferences, expanding the network for potential sites.

Qualifications:

  • A doctoral degree (M.D., PharmD, or PhD) is required.

  • Previous experience in clinical research within Pharma, Biotech, or CRO environments is highly preferred.

  • Broad knowledge of scientific and medical concepts related to clinical development.

  • Strong communication and negotiation skills with the ability to influence and persuade.

  • Ability to work independently and collaboratively, demonstrating critical thinking and operational expertise.

  • Proficiency in English and the local language.

  • Willingness to travel up to ~75%, including to the United States.

Work Arrangement:

  • This position is remote with the possibility of office engagements. Travel is required up to ~75%.

Compensation & Benefits:

  • Competitive salary based on experience and qualifications.

  • Comprehensive health insurance options tailored to support you and your family.

  • Retirement planning tools and options for long-term financial stability.

  • Global Employee Assistance Programme (LifeWorks), offering 24/7 access to mental, emotional, and physical well-being services.

  • Life assurance and flexible, country-specific benefits such as:

    • Childcare vouchers

    • Bike-to-work schemes

    • Discounted gym memberships

    • Health assessments

    • Subsidized public transport

Diversity & Inclusion:
ICON is committed to providing an inclusive and accessible environment. We ensure equal employment opportunities regardless of race, religion, gender, sexual orientation, gender identity, national origin, disability, or veteran status.