Clinical Research Coordinator I / II
Core
Lead one main supportive care clinical research study while collaborating across various research projects and initiatives at a cancer centre.
Role type
Clinical Research Coordinator
Builds
Supportive care clinical research studies and academic activities
Domain
Healthcare / Oncology / Clinical Research
Deliverable
client delivery
Required skills
Clinical study coordination, patient recruitment and screening, informed consent processes, data collection and cleaning, regulatory document management, research ethics submissions, basic statistical analysis, protocol development, scientific writing, team training and supervision
Preferred skills
Oncology research experience, medical terminology proficiency, human anatomy knowledge, grant management, statistical software proficiency, REDCap data collection platforms, clinical research certification (SOCRA/ACRP)
Technologies
REDCap, MS Office (Word, Excel, Outlook), statistical software
Responsibilities
Recruit and screen study participants; coordinate visits and data collection per protocol; manage data entry and investigator study files; prepare manuscripts, abstracts, and grant submissions; supervise research students; facilitate meetings and ethics submissions
Seniority
Mid-level, hands-on IC
