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Clinical Research Associate - Oncology

2+ 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:

Clinical Research Associate - Oncology - Halifax (Remote)


Location:

Remote (Halifax, Canada)


Job ID:

2025-117436


Department:

Clinical Monitoring – ICON Strategic Solutions


Job Type:

Full-Time, Remote


Application Contact:

Name: Monica Hawkins
Options: View other roles or send a message via the application platform


Job Description:

As a Clinical Research Associate (CRA), you will oversee multiple oncology trials, ensuring high-quality execution while providing leadership and mentorship to junior team members. Your responsibilities include creating essential study documents, ensuring alignment with study objectives, reviewing reports, and supporting trial management. You will represent Site Managers and Lead Trial Managers (LTMs) in meetings, assist in budgeting and contract negotiations, and collaborate with country teams to drive successful clinical trial outcomes.


Key Responsibilities:

  • Oversee multiple oncology trials and ensure high-quality execution

  • Lead and mentor junior site management team members

  • Develop study start-up documents and represent Site Managers in meetings

  • Review reports (e.g., SQV, SMV, SCV) for sites managed by other team members

  • Support country budget development and contract negotiations

  • Drive patient recruitment strategies and collaborate with investigators

  • Maintain compliance with Metrics/KPIs outlined in the Quality Oversight Plan (QOP)

  • Ensure alignment with study objectives and assist with ASV activities

  • Provide leadership and guidance on risk-based/analytical monitoring approaches


Required Qualifications:

  • Education: Minimum B.Sc., R.N., or equivalent degree (preferably in Biological Sciences)

  • Experience:

    • At least 2 years monitoring clinical trials in the pharmaceutical industry

    • Experience in oncology (e.g., Hematology, Prostate Cancer, Lung Cancer, Early Development - Phase 1)

    • Proficiency in clinical trial systems (e.g., CTMS, EDC, TMF, IWRS)

  • Skills:

    • Knowledge of Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements

    • Ability to collaborate effectively with site staff and investigators

    • Strong communication skills for managing study sites remotely and in person

    • Ability to work independently and influence site teams

  • Travel: Up to 50% regional travel required

  • Location: Must be legally authorized to work in Canada

  • Visa: No sponsorship required now or in the future


What ICON Offers:

  • Competitive salary and performance rewards

  • Health insurance, retirement planning, and life assurance

  • Global Employee Assistance Program for 24/7 support

  • Paid annual leave, plus additional flexible benefits (e.g., childcare, gym memberships, travel passes)
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    Explore ICON Benefits


Diversity & Inclusion Commitment:

ICON is dedicated to fostering an inclusive and accessible environment for all candidates, with equal consideration for employment opportunities.