Clinical Research Associate - Oncology - Canada (No Travel)*

Pharmaceutical Research Associates, Inc; Canada; Remote; CAD 70,000 - 90,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Research Associate (CRA) to manage oncology trials. Responsibilities include mentoring junior staff, overseeing trial processes, and ensuring compliance with regulations. The ideal candidate will have a relevant degree and experience in clinical trials, particularly in oncology. This role offers a chance to contribute to significant healthcare advancements while enjoying a supportive work culture with diverse benefits.

Benefits

Annual leave entitlements

Health insurance options

Retirement planning

Employee Assistance Programme

Life assurance

Childcare vouchers

Gym discounts

Qualifications

• 2-3 years’ experience in pharmaceutical industry clinical trials monitoring.
• 1-3 years’ experience in Oncology trials.

Responsibilities

• Managing multiple oncology trials.
• Mentoring and coaching junior team members.
• Supporting budget development and contract negotiations.

Skills

Communication

Leadership

Risk-based monitoring

Education

Bachelor’s degree (B.S.)

Nursing (R.N.)

Biological Sciences

Tools

CTMS

EDC

eTMF

IWRS

safety reporting

Job description

Overview

As a CRA, you will join the world’s largest and most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

What will you be doing?

• Managing multiple oncology trials
• Demonstrating leadership through involvement in initiatives and acting as SME for systems and processes
• Mentoring and coaching junior team members
• Training other Study Managers (SMs) and acting as Lead SM
• Developing site start-up documents, including SIV agendas
• Reviewing study documents and providing input as SM voice
• Representing Lead Trial Managers (LTMs) or SMs in meetings
• Taking over LTM report reviews for sites managed by other SMs in the same trial
• Supporting budget development and contract negotiations with CCS colleagues
• Assisting with site verification visits (ASV)
• Monitoring metrics and KPIs as outlined in the Quality Oversight Plan

Interfaces – Primary and Others:

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

Qualifications

What do you need to have?

• Bachelor’s degree (B.S.), Nursing (R.N.), or equivalent in Biological Sciences
• Located in Canada
• Experience in remote monitoring of US clinical trials
• 2-3 years’ experience in pharmaceutical industry clinical trials monitoring
• 1-3 years’ experience in Oncology trials
• Knowledge across therapeutic areas
• Risk-based monitoring experience (asset)
• Ability to drive patient recruitment strategies
• Strong communication skills and ability to work independently
• Proficiency with systems like CTMS, EDC, eTMF, IWRS, safety reporting
• In-depth knowledge of GCP, ICH guidelines, and local regulations
• Legal authorization to work in Canada; no sponsorship required

What ICON can offer you: We prioritize building a diverse culture that rewards high performance and nurtures talent. Benefits include:

• Annual leave entitlements
• Health insurance options
• Retirement planning
• Employee Assistance Programme
• Life assurance
• Optional benefits like childcare vouchers, gym discounts, etc.

Visit our careers website for more: https://careers.iconplc.com/benefits

ICON is committed to inclusion and providing a workplace free of discrimination and harassment. All qualified applicants will be considered without regard to 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—perhaps you’re exactly what we’re looking for!