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Clinical Research Associate - Oncology - Western Canada (remote)

Lensa

United States

Remote

USD 70,000 - 90,000

Full time

Yesterday
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Job summary

A leading company in clinical research is seeking a Clinical Research Associate for Oncology trials. This remote role involves overseeing multiple trials, mentoring team members, and ensuring compliance with regulations. Ideal candidates have experience in US trials and Oncology, along with strong communication skills. The company offers a diverse culture and comprehensive benefits, including health insurance and retirement planning.

Benefits

Various annual leave entitlements
Health insurance options
Retirement planning
Global Employee Assistance Programme
Life assurance
Childcare vouchers
Gym discounts
Travel passes

Qualifications

  • 2-3 years’ experience in monitoring pharmaceutical clinical trials.
  • 1-3 years' experience in Oncology trials.
  • Legal authorization to work in Canada; no sponsorship needed.

Responsibilities

  • Work on multiple trials within Oncology.
  • Mentor and coach junior team members.
  • Develop site start-up documents.

Skills

Communication
Influencing Skills
Knowledge of Therapeutic Areas
Risk-Based Monitoring

Education

B.S. in Biological Sciences
R.N.

Tools

CTMS
EDC
eTMF
IWRS
Safety Reporting

Job description

Clinical Research Associate - Oncology - Western Canada (remote)

Lensa is the leading career site for job seekers at every stage of their career. Our client, ICON Clinical Research, is seeking professionals. Apply via Lensa today!

What will you be doing?

  1. Work on multiple trials within Oncology.
  2. Demonstrate leadership through involvement in initiatives and serve as SME to systems/processes.
  3. Mentor and coach junior team members.
  4. Act as Lead SM, training other SMs on studies.
  5. Develop site start-up documents, including SIV agendas.
  6. Review study documents, providing the SM "voice" (e.g., Monitoring Guidelines).
  7. Represent LTMs or SMs in meetings.
  8. Take over LTM report reviews for sites assigned to other SMs within the same trial.
  9. Support country budget development and contract negotiations with CCS colleagues.
  10. Assist with ASV activities.
  11. Monitor metrics and KPIs as outlined in the QOP document.

Interfaces – Primary/Other

  1. Primary: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager, Central Study Team.
  2. Others: Study Physician, Regional Quality & Compliance, Local Drug Safety Officer, Site Manager team, Investigators, and site personnel.

What do you need to have?

  1. B.S., R.N., or equivalent degree, preferably in Biological Sciences.
  2. Located in Canada.
  3. Experience working on US trials remotely.
  4. 2-3 years’ experience in monitoring pharmaceutical clinical trials.
  5. 1-3 years' experience in Oncology trials.
  6. Knowledge of therapeutic areas, risk-based monitoring, and systems like CTMS, EDC, eTMF, IWRS, safety reporting.
  7. Strong communication, influencing skills, and ability to work independently.
  8. In-depth knowledge of GCP, ICH guidelines, and local regulations.
  9. Legal authorization to work in Canada; no sponsorship needed.

What ICON Can Offer You

We prioritize a diverse culture that rewards high performance and nurtures talent. Our benefits include:

  • Various annual leave entitlements.
  • Health insurance options.
  • Retirement planning.
  • Global Employee Assistance Programme.
  • Life assurance.
  • Optional benefits like childcare vouchers, gym discounts, travel passes.

Visit our careers website for more info.

At ICON, inclusion & belonging are fundamental. We are committed to a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly what we’re looking for!

Seniority level
  • Mid-Senior level
Employment type
  • Full-time
Job function
  • Research, Analyst, and Information Technology
Industries
  • IT Services and IT Consulting
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