Data Manager (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-Time 2026-19103 (2026-19103)

Sunnybrook; Toronto; On-site; CAD 65,000 - 90,000; Full time

Benefits offered by this job

Health benefits plan

Pension

Paid time off

Job summary

Sunnybrook's Odette Cancer Center Clinical Research program seeks a dedicated team member to support GI Oncology disease site group with active studies, databases, and trials. The role is full-time, on-site at Sunnybrook Bayview campus, and includes health benefits, pension, and paid time off.

You will collect data, enter into EDC systems, track patient visits and enrollment, coordinate with sponsors and CROs, and assist with trial activations and documentation.

Qualifications

• Requires a health-related diploma/certificate or university degree.
• 1–2 years of clinical research experience preferred or equivalent.
• Knowledge of ICH guidelines, Good Clinical Practice, and dangerous goods transport.
• Experience in processing and shipping blood samples.
• Experience in informed consent process a plus.
• Ability to understand trial protocols and laboratory manuals.
• Knowledge of ethics review process.
• Proficiency in MS Office and adaptability to new online systems (EDC, portals).

Responsibilities

• Assist in data collection and data entry on electronic data capture systems and databases.
• Internally track trial-related data and metrics (patient visits, enrollment logs, etc).
• Resolve sponsor queries.
• Prepare for and participate in remote and on-site monitoring visits, audits, inspections.
• Create or complete trial-related forms; maintain trial master file documentation.
• Communicate with patients, multidisciplinary teams, external hospitals, and health services to obtain study information.
• Coordinate with sponsors and CROs.
• Prepare and ship blood, urine, tissue specimens.
• Support new trial activation activities and ethics submissions.
• Archive trial records for completed studies.
• May involve patient-facing tasks such as questionnaires or obtaining vital signs.
• Maintain knowledge of regulations, SOPs, and institutional guidance.
• Perform additional trial-related tasks as needed by the team; may involve walking with documents.

Skills

Data entry

Data management

Communication

MS Office

EDC systems

Education

Health-related Diploma/Certificate or University Degree

Tools

MS Office

EDC databases

Job description

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 Clinical Trials Manager and Budget & Operations Coordinator work with 35+ physicians actively participating in clinical research and 55+ OCC clinical research disease site-specific staff. Our program is comprised of 12 disease site groups; Breast, CNS, NETS, GI, GU medical, GU radiation, Gynecology, Head & Neck, Hematology, Lung, Melanoma and Early Phase I-II trials; as well as the pan-Canadian initiative, Canadian Cancer Clinical Trials Network (3CTN). The goal of this position is to assist the GI Oncology Disease Site Group with the maintenance of their active oncology clinical research studies, databases, and trials. This position is a full-time position working weekdays on-site at Sunnybrook, Bayview campus. This position is entitled to health benefits plan, pension, and paid time off/sick days.

General Responsibilities Include, But Are Not Limited To

• Assisting in collection of data, data entry on electronic data capture systems (EDCs) and databases
• Internal tracking of trial-related data and metrics (patient visits, enrollment logs, etc)
• Resolving sponsor queries
• Preparing for and participating in remote and on-site monitoring visits, audits, inspections
• Creation of or completion of trial-related forms; maintaining trial master file documentation
• Communicating with patients, multidisciplinary hospital team members, external hospitals, and other health services to obtain medical information for study participants
• Communication with external partners such as sponsors and CROs
• Preparing, processing, and safe shipment of blood, urine, tissue specimens
• Supporting new trial activation activities such as sponsor communications, departmental communication, ethics submissions, and administrative documentation
• Archiving trial records for completed studies
• May involve some patient-facing work such as administering questionnaires, collecting medical information, obtaining vital signs, or consenting patients to research studies
• Maintain training and working knowledge of current regulations, clinical trial-related guidance documents, and institutional SOPs, policies, and working instructions
• Trial-related tasks and activities beyond what is listed on the posting as required by the trial team and as delegated by the Principal Investigator(s)
• May involve walking or pushing a cart of documents/supplies across Sunnybrook Bayview campus or lifting items less than 10kg

Research 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
• In-depth knowledge of ICH guidelines, Good Clinical Practice, and transportation of dangerous goods
• Proven experience in processing and shipping blood samples
• Experience in the informed consent process and working directly with research participants an asset
• Ability to understand clinical trial protocols and laboratory manuals
• Knowledge of the ethics review process
• 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 or experience reviewing patient health records

Interpersonal Qualifications/Skills

• Well-developed organizational and time management skills
• Excellent team work with a strong “can-do” attitude to build working relationships
• Excellent oral and written communication skills; using professional communication tactics across multidisciplinary teams and external stakeholders
• Ability to follow verbal instruction, written procedures, and apply trainings in practice
• Demonstrated accurate and efficient work habits with close attention to detail and high quality of work
• Strong analytical skills and ability to apply critical thinking for problem solving
• Reliable attendance and punctuality
• Strong accountability for independent workload
• Demonstrated professional behaviours and ethical integrity
• Strong cultural competency and ability to work respectfully in diverse team environments

Last day for applications: Until Filled