Clinical Research Associate - Oncology - Western Canada (remote)

Lensa; United States; Remote; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Clinical Research Associate specializing in Oncology to manage multiple trials remotely. This role involves mentoring junior staff, developing critical documentation, and collaborating with various stakeholders to ensure successful trial execution. With a focus on diversity and well-being, the company offers competitive salaries and a range of benefits aimed at fostering a healthy work-life balance. If you are passionate about clinical research and want to make a meaningful impact in the healthcare sector, this opportunity is perfect for you.

Benefits

Health insurance options

Retirement plans

Global Employee Assistance Programme

Life assurance

Gym discounts

Childcare vouchers

Various annual leave entitlements

Qualifications

• 2-3 years’ experience in clinical trial monitoring in the pharmaceutical industry.
• In-depth knowledge of GCP, ICH guidelines, and local regulations.

Responsibilities

• Managing multiple oncology trials and mentoring junior team members.
• Developing site start-up documents and reviewing study documents.

Skills

Clinical Trial Monitoring

Oncology Knowledge

Communication Skills

Risk-Based Monitoring

Patient Recruitment

Education

Bachelor’s degree in Biological Sciences

Tools

CTMS

EDC

eTMF

IWRS

Job description

Clinical Research Associate - Oncology - Western Canada (remote)

2 days ago Be among the first 25 applicants

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!

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

What will you be doing?

• Managing multiple oncology trials
• Demonstrating leadership through involvement in initiatives and serving as SME for systems and processes
• Mentoring and coaching junior team members
• Acting as Lead SM, training other SMs on studies
• Developing site start-up documents, including SIV agendas
• Reviewing study documents, providing the SM’s perspective (e.g., Monitoring Guidelines)
• Representing LTMs or SMs in meetings
• Handling LTM role reports review (SQV, SMV, SCV) for sites managed by other SMs
• Supporting country budget development and contract negotiations with CCS colleagues
• Assisting with ASV activities
• Monitoring metrics and KPIs as outlined in the Quality Oversight Plan (QOP)

Interfaces – Primary/Other

• Primary: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager, and Central Study Team
• Other: Study Physician, Quality and Compliance Managers, Local Drug Safety Officers, Site Teams, Investigators, and site personnel

What do you need to have?

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

What ICON Can Offer You

ICON values diversity and high performance, offering competitive salaries and benefits focused on well-being and work-life balance, including:

• Various annual leave entitlements
• Health insurance options
• Retirement plans
• Global Employee Assistance Programme
• Life assurance
• Optional benefits like childcare vouchers, gym discounts, and more

Learn more at: https://careers.iconplc.com/benefits

ICON is committed to inclusion and equal opportunity. All qualified applicants will be considered without discrimination based on race, gender, or other protected characteristics.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Research, Analyst, and IT

Industries

• IT Services and Consulting