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)
🔗 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.
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