Data Manager - Toronto, Canada - Sunnybrook Health Sciences Centre

Sunnybrook Health Sciences Centre

Verified Company

Toronto, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

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)).

The goal of this position is to assist the Genitourinary medical oncology Disease Site Group with the ongoing activities of their clinical research studies and trials.

This position is for a regular fulltime position. This position is entitled to health benefits plan, pension, and paid time off/sick days.

General responsibilities include, but are not limited to:

Data entry on electronic data capture systems (EDCs) and databases
Internal tracking of trialrelated data (patient visits, enrollment logs, etc)
Resolving sponsor queries
Preparing for and participating in remote and onsite monitoring visits
Completing trialrelated 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
Trialrelated 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 12 years of related professional or practical experience, in clinical research preferred, or the equivalent combination of education and professional experience
Welldeveloped organizational and time management skills
Indepth 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 "cando" attitude
Excellent oral and written communication skills
Demonstrated accurate and efficient work habits with close attention to detail
Strong analytical and problem solving skills
Familiarity with medical terminology