Clinical Research Associate - Cross TA / ONC - Western Canada (BC / Alberta)

ICON Strategic Solutions; Canada; Remote; CAD 60,000 - 100,000; Full time

Job summary

An established industry player seeks a Clinical Research Associate to oversee multiple clinical trials across therapeutic areas, particularly in oncology. This role emphasizes leadership, collaboration, and compliance with study protocols while ensuring high-quality execution of clinical trials. The ideal candidate will have a strong background in clinical trial monitoring and a passion for driving patient recruitment strategies. Join a dynamic team that values diversity and offers competitive benefits focused on well-being and work-life balance. This is a fantastic opportunity to make a significant impact in the pharmaceutical industry.

Benefits

Health Insurance

Retirement Plans

Employee Assistance Programs

Work-Life Balance Initiatives

Qualifications

• 2+ years of experience monitoring clinical trials in the pharmaceutical industry.
• Knowledge of oncology and hematology preferred.

Responsibilities

• Oversee multiple clinical trials ensuring high-quality execution.
• Provide mentorship to junior team members and develop study documents.

Skills

Clinical Trial Monitoring

Leadership

Communication Skills

Risk-Based Monitoring

Patient Recruitment Strategies

Education

B.Sc. in Biological Sciences

Registered Nurse (R.N.)

Tools

CTMS

EDC

TMF

IWRS

Safety Reporting Tools

Job description

Clinical Research Associate - Cross TA / ONC - Western Canada (BC / Alberta)

Join ICON Strategic Solutions as a Clinical Research Associate - Cross TA / ONC - Western Canada (BC / Alberta).

Overview

Become part of the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence.

Responsibilities

• Oversee multiple clinical trials (cross TA/ONC), ensuring high-quality execution.
• Provide leadership and mentorship to junior team members.
• Act as Lead SM, training and guiding Site Managers on study protocols.
• Develop study start-up documents, including SIV agendas.
• Represent Site Managers and Lead Trial Managers in meetings.
• Ensure the SM perspective is reflected in study documents like Monitoring Guidelines.
• Review reports for sites assigned to other SMs within the same trial.
• Support country budget development and contract negotiations.
• Assist with ASV activities and ensure alignment with study objectives.
• Maintain compliance with Metrics/KPIs outlined in the QOP.

Qualifications

• Remote position based in Western Canada (BC or Alberta).
• Minimum of a B.Sc., R.N., or equivalent in Biological Sciences.
• At least 2 years monitoring clinical trials in the pharmaceutical industry.
• Knowledge of therapeutic areas, especially oncology, Hematology, Prostate Cancer, Lung Cancer, Phase 1 studies, is preferred.
• Knowledge of risk-based/analytical monitoring approaches is a plus.
• Proficiency in systems like CTMS, EDC, TMF, IWRS, and safety reporting tools.
• Ability to drive patient recruitment strategies.
• Strong collaboration, communication, and influencing skills.
• Ability to work independently and as part of a team.
• Understanding of GCP, ICH guidelines, and local regulations.
• Up to 50% regional travel.
• Legally authorized to work in Canada without future sponsorship needs.

What ICON Offers

Competitive salary and benefits focused on well-being and work-life balance, including health insurance, retirement plans, employee assistance programs, and more. Visit our benefits page for details.

ICON values diversity, inclusion, and accessibility. We are committed to an equitable workplace and provide accommodations during the application process.

Additional Information

Seniority level: Mid-Senior level

Employment type: Full-time

Job function: Research, Analyst, IT

Industry: Pharmaceutical Manufacturing