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Clinical Trial Liaison

0-2 years
Not Disclosed
10 April 17, 2025
Job Description
Job Type: Hybrid Education: M.D., PharmD or PhD 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

Position: Clinical Trial Liaison
Location: Melbourne, Australia (Home-based)
Job Code: JR128616
Company: ICON plc - Full Service & Corporate Support


About ICON:

ICON plc is a leading global healthcare intelligence and clinical research organization committed to driving innovation and excellence. We offer a dynamic environment where our people are the driving force behind the future of clinical development.


Role Overview:

ICON is currently seeking a Clinical Trial Liaison (CTL) to join their team in Melbourne, Australia. The CTL will play a critical role in ensuring the success of clinical trials by providing scientific and clinical support to investigators and site staff. This role involves engaging with key stakeholders, building relationships with clinical sites, and driving patient recruitment strategies.


Key Responsibilities:

  • Scientific and Clinical Support: Provide expertise and support to study sites to ensure a clear understanding of the trial’s design, procedures, and goals.

  • Recruitment Strategy: Develop and optimize strategies at the site and study level to enhance patient recruitment and ensure successful trial outcomes.

  • Networking: Build and maintain relationships with key stakeholders, including medical and scientific leaders, and advocates.

  • Collaboration: Work cross-functionally with internal teams, external stakeholders, and investigators to align on trial objectives and best practices.

  • Travel: Engage on-site and at industry meetings/conferences, requiring up to 75% travel.

  • Critical Thinking: Provide operational expertise and apply knowledge to real-world trial challenges, ensuring smooth execution.


Qualifications:

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

  • Experience: Prior experience in clinical research, particularly in pharma, biotech, or CRO environments in scientific and/or clinical operations.

  • Skills:

    • Strong communication and presentation skills, particularly in local medical languages.

    • In-depth scientific and medical knowledge with an understanding of clinical development processes.

    • Excellent interpersonal skills to build relationships with internal and external stakeholders.

    • Ability to work independently and collaboratively, demonstrating proactive behavior.


What ICON Can Offer You:

  • Competitive Salary: Along with additional benefits designed to support well-being and work-life balance.

  • Health Insurance: A variety of offerings for you and your family’s needs.

  • Retirement Planning: Competitive options for long-term savings and confidence in planning.

  • Global Support: Access to the LifeWorks Employee Assistance Programme, offering a global network of specialized professionals.

  • Flexible Benefits: Country-specific benefits, including childcare vouchers, gym memberships, subsidized travel passes, etc.


Inclusion Statement:
ICON values diversity and inclusion, providing a workplace free from discrimination and harassment. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.


To Apply:
Visit the slug link to apply for the role:
clinical-trial-liaison-melbourne-jr128616