Data Manager (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-time 2024-9314

The goal of this position is to assist the Hematology Oncology Disease Site Group with the ongoing activities of their clinical research studies and trials.  This position is for a regular full-time position. This position is entitled to health benefits plan, pension, and paid time off/sick days. 

Summary of Duties and Responsibilities:

The Odette Cancer Center (OCC) Clinical Research program is part of Sunnybrook Research Institute’s (SRI) ongoing commitment to participate in innovative and high quality clinical research.

Within OCC Clinical Research, the Quality Assurance and Education Manager, Operations Assistant Manager, and Budget & Operations Coordinator, work with 50+ physicians actively participating in clinical research and 50+ OCC clinical research disease site-specific staff. Our program is comprised of 10 disease site groups; Breast, CNS, GI, GU, Gynecology, Head & Neck, Hematology, Lung, Melanoma and Palliative; as well as 2 pan-Canadian initiatives (Personal My Treatment & The Canadian Cancer Clinical Trials Network (3CTN)).

General responsibilities include, but are not limited to:

• Data entry on electronic data capture systems (EDCs) and databases
• Internal tracking of trial-related data (patient visits, enrollment logs, etc)
• Resolving sponsor queries
• Preparing for and participating in remote and on-site monitoring visits
• Completing trial-related forms, maintaining trial master file documentation
• Communicating with patients, hospitals, and other health services to obtain medical information for study participants
• Assisting in recruitment of study participants and collection of study data
• Consenting of study participants for enrollment onto research studies and trials
• Preparing, processing, and safe shipment of blood, urine, tissue specimens
• Trial-related administrative tasks and other activities beyond what is listed on the posting as required by the trial team and as delegated by the Principal Investigator

Qualifications/Skills:

• Requires the successful minimum completion of a Community College Diploma/Certificate or University Degree in a health related discipline
• A minimum of 1-2 years of related professional or practical experience, in clinical research preferred, or the equivalent combination of education and professional experience
• Well-developed organizational and time management skills
• In-depth knowledge of ICH guidelines and Good Clinical Practice an asset
• Proven experience in processing and shipping blood samples
• Excellent team work and independent work habits with a strong “can-do” attitude
• Excellent oral and written communication skills
• Demonstrated accurate and efficient work habits with close attention to detail
• Strong analytical and problem solving skills
• Strong working capability of MS Office and ability to quickly adapt to new online systems and applications (EDC databases, document portals, etc)
• Familiarity with medical terminology

Last day for applications: Until Filled

Interested candidates please apply online.  Please include your first and last name in the title of your submitted resume file.