8 meilleures offres (oncology hematology, mississauga, on) (à pourvoir)

Clinical Research Associate II (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-Time 2026-17987
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Expérience en laboratoire
- Microsoft Office
- Bases de données
- Congés payés
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Medical Affairs Manager, Rare Disease, Canada
Medison Pharma —Toronto, ON
- De 150 000 $ à 180 000 $ par an
- Temps plein
- Médecine
- Doctorat
- Maîtrise
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il y a 2 jours
National Business Manager, Oncology
Sanofi —Toronto, ON
- De 125 300 $ à 208 800 $ par an
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- Télétravail
- Doctorat
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Director, Marketing Cell Therapy
Gilead Sciences —Mississauga, ON
- De 170 255 $ à 220 330 $ par an
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- Maîtrise
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Key Account Manager, Multiple Myeloma - Central Ontario
Sanofi —Toronto, ON
- De 94 700 $ à 157 800 $ par an
- Fins de semaine au besoin
- Télétravail
- Logiciels de GRC/CRM
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Director, Marketing Canada / Directeur, Marketing Canada
BeiGene —Toronto, ON
- De 164 500 $ à 205 600 $ par an
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- Travail hybride
- Microsoft Powerpoint
- Bilingue
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il y a 9 jours
Title Sr. Product Manager, Canada
Recordati —Toronto, ON
- Fins de semaine au besoin
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il y a 13 jours
Sr Business Unit Director Cell Therapies - Canada
Gilead Sciences —Mississauga, ON
- De 262 650 $ à 339 900 $ par an
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- Médecine
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Patient Administrative Associate - Complex Malignant Hematology - Temporary Part-Time - 2026-18244
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OR data entry at 106 net keystrokes per minute. Coordinating electronic physician orders with applicable software; One year of Community College required.
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Clinical Laboratory Geneticist - Molecular Diagnostics - Casual 2025-14126
Sunnybrook Health Sciences Centre —Toronto, ON
Leading new genetic and molecular assay development, validation and implementation including making recommendations regarding methodology and equipment for…
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Clinical Research Associate II (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-Time 2026-17987

Sunnybrook Health Sciences Centre -
Toronto, ON

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Détails du poste

Temps plein

Profil recherché

Certificat collégial
Expérience en laboratoire
Microsoft Office
Bases de données
Esprit d'analyse
Baccalauréat
Marchandises dangereuses
Contrats
Communication
Diplôme d'études collégiales (hors Québec)
Terminologie médicale
Compétences en communication
Gestion du temps

Description complète du poste

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 GU Med Oncology Disease Site Group with the maintenance of their active oncology clinical research studies, databases, and trials. This position is for 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. The CRA II will report to the team Physician Site Lead, team Supervisor, and PIs. The CRA II may also work closely with an interdisciplinary team including the Clinical Trials Manager, Operation Leads, and all other OCC Clinical Research Program staff.

Primary responsibilities include but are not limited to:

Independently lead the management of several complex Health Canada-regulated interventional clinical trials, academic clinical trials, and other research projects
Requesting, handling, and/or processing laboratory specimens (blood, urine, tissue)
Consenting patients, reviewing trial eligibility criteria and medical records
Applying clinical trial protocol requirements into patient & data activities such as documenting medical history, medications and adverse events from patients; reporting Serious Adverse Events
Scheduling and conducting patient appointments, completing qualify of life questionnaires with patients
Conducting measurements on patients including vital signs, ECGs, height/weight measurements
Communication with various hospitals and health service facilities to obtain medical information

Understanding requirements of the ethics review process, completing REB submissions and documentation updates
Data entry and resolving sponsor queries
Scheduling and participating in monitoring visits, sponsor audit visits, regulatory inspections
Maintaining documentation as part of the trial master file, creating source documents
Communication with internal hospital departments or liaising with Contract Research Organizations (CROs) and Sponsors/Trial Lead hospitals on behalf of your principal investigators
Tracking of trial metrics, and other research-related activities within the needs of the team
Leading the activation activities of new clinical trials with external sponsors and CROs, and the closure of completed trials

The successful candidate will be an eager team player who meets the following qualifications/skills:

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 3-5 years of related professional or practical experience, including at least 3 years in clinical research, or the equivalent combination of education and professional experience; Health Canada-regulated clinical trial experience preferred
SoCRA/CCRP certification an asset; oncology clinical trial experience an asset
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
Ability to understand and apply clinical trial protocols and laboratory manuals
Knowledge and experience in the ethics review and submission process
Strong working capability of MS Office and ability to quickly adapt to new online systems and applications, accurately entering data, and resolving queries (EDC databases, document portals)
Experience maintaining clinical trial documentation in a Trial Master File, creating source documentation
Experience in patient-facing communication, including obtaining AE/SAE or other trial-related medical information
Familiarity with medical terminology or experience reviewing patient health records
Experience or familiarity with research contracts and budget management an asset
May be involved in training new team members or assisting junior staff on team

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 complex problem solving independently
Reliable attendance and punctuality
Strong accountability for independent workload; maintain multiple projects with minimal direct supervision; develop and maintain tools or trackers to enhance task performance
Demonstrated professional behaviours and ethical integrity
Strong cultural competency and ability to work respectfully in diverse team environments

Interested candidates please apply online and complete all screening questions in the online portal.

Last day for applications: Until Filled

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Clinical Research Associate II (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-Time 2026-17987

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