Research Coordinator - Oncology

One of Canada's Best Diversity Employers and Greater Toronto's Top Employers for many consecutive years, William Osler Health System (Osler) provides a safe and supportive health care network to grow your career.

Osler is nationally recognized for its commitment to patient safety and is Accredited with Exemplary Standing, the highest rating a Canadian hospital can receive.

As a major Ontario hospital system, and home to some of the biggest specialty and emergency departments in the country, Osler serves the 1.3 million residents of Brampton, Etobicoke and surrounding communities.

We are proud to offer you incredible exposure to best-in-class health care delivery and challenging hands-on opportunities to stay at the top of your game.

A hospital system built for and by the community, we continue to expand our services to meet the needs of a growing population, creating opportunities for increased hands-on skills development, cross-department training and promotional opportunities.

Guided by our accomplished senior leadership team, together we are driving our vision of patient-inspired health care without boundaries.

At Osler, we invest in careers that go beyond where health care professionals like you can achieve their goals and find deep personal and professional fulfillment.

Join our team today!

We’re looking for an experienced Research Coordinator (RC) to join our growing team.

The RC plays an integral role in the Oncology Research Department.

This is an exciting and challenging position, conducting multicentre centred randomized clinical trials.

This position requires the ability to adhere to research protocol and work with the Investigator and other team members to carry out various aspects of conducting a clinical trial.

The Oncology Research Coordinator reports to the Manager of Research, Oncology, with accountability to the Oncology leadership team.

• Patient screening, recruitment and consenting according to the study protocol
• Assist Investigators in the initiation of new research
• Ensure completion of eligibility requirements prior to enrollment and randomization
• Facilitate and coordinate the planned cancer treatment schedule for each trial patient
• Carrying out all study procedures including patient assessments, coordinating laboratory, pharmacy, and diagnostic activities pertaining to study
• Specimen preparation and shipping to external labs as per IATA regulations