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Clinical Research Associate - Oncology

2-3 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 (Western Canada - Remote)


Location:

Remote – Vancouver, Calgary, Winnipeg, Canada (Work on US trials)


Job ID:

2025-117283


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 work on multiple oncology trials with a focus on high-quality execution. This role includes mentoring junior team members, supporting study documents, managing site relationships, and assisting in monitoring oncology trials for the US market remotely.


Key Responsibilities:

  • Oversee and monitor multiple oncology trials ensuring quality execution

  • Lead and mentor junior Site Managers (SM), providing training and guidance

  • Develop essential study documents such as Site Initiation Visit (SIV) agendas

  • Represent Site Managers and Lead Trial Managers (LTMs) in key meetings

  • Ensure SM’s input is reflected in study documents like Monitoring Guidelines

  • Review site reports (SQV, SMV, SCV) for sites assigned to other SMs

  • Support country budget development and contract negotiations with CCS colleagues

  • Assist with ASV and ensure alignment with study objectives

  • Maintain compliance with KPIs and metrics outlined in the Quality Oversight Plan (QOP)


Interfaces:

  • Primary: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager, Central Study Team

  • Other: Investigators, Site Coordinators, Site Pharmacists, Local Drug Safety Officers, Regional Compliance Teams


Required Qualifications:

  • Location: Remote, must be based in Western Canada (Vancouver, Calgary, Winnipeg)

  • Must be located in Canada and legally authorized to work in Canada

  • Bilingual proficiency not required, but knowledge of English required

  • Minimum of a B.Sc., R.N., or equivalent degree, preferably in Biological Sciences

  • At least 2-3 years of experience in monitoring pharmaceutical clinical trials

  • 1-3 years of experience specifically in oncology trials

  • Experience with risk-based/analytical monitoring (preferred)

  • Proficiency in clinical trial systems (CTMS, EDC, TMF, IWRS, safety reporting tools)

  • Ability to drive patient recruitment strategies at assigned sites

  • Strong communication skills to manage study sites effectively both remotely and in-person

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

  • Up to 50% travel may be required for regional monitoring

  • Must not require future visa sponsorship


What ICON Offers:

  • Competitive salary and recognition for high performance

  • Health insurance coverage for you and your family

  • Retirement planning and savings opportunities

  • Global Employee Assistance Program (TELUS Health)

  • Paid annual leave and work-life balance policies

  • Country-specific benefits such as childcare vouchers, gym memberships, and health assessments
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    Explore ICON Benefits


Diversity & Inclusion Commitment:

ICON is committed to fostering a diverse, inclusive workplace that promotes a sense of belonging for all employees, with equal opportunity for all qualified candidates.