Research Coordinator

Hamilton Health Sciences • Hamilton, ON

4h

About The Position

The Juravinski Cancer Centre (JCC) Clinical Trials Department (CTD) is seeking a Trial Activation Coordinator (TAC). Under the direction of the CTD Manager, the TAC provides a full range of administrative support to facilitate the efficient and effective activation of new clinical trials. This includes the coordination and completion of the study activation process and quality assurance oversight in a fast-paced, deadline-orientated environment. The TAC must be able to communicate effectively with CTD members, investigators, study sponsors, research ethics board staff, and other staff at institutions throughout Ontario in addition to providing functional guidance to ethics secretaries working within the Department.

Requirements

• University degree in a health sciences-related field
• Three (3) years’ experience in a clinical research setting (oncology clinical research preferred)
• Knowledge of clinical research, research ethics and regulatory processes preferred
• Clinical Trials Research Coordinator Course (CRTC) and/or Certification as a Clinical Research Professional/Coordinator
• Sound knowledge of the regulations and guidelines governing clinical research, including the Tri-Council Policy Statement, Health Canada regulations, ICH Good Clinical Practice guidelines, FDA and OHRP regulations, and privacy legislation
• Proficient understanding of medical terminology
• Exceptional computer skills including MS Word, Excel, and Outlook
• Knowledgeable of electronic document management systems
• Superior organizational, project and time management skills
• Attention to detail is a must
• Well-developed oral and written communication, and interpersonal skills
• Strong analytical, critical thinking, organizational and time management skills
• Demonstrated ability to work both independently and as part of a team
• Ability to prioritize and work effectively in a fast-paced, deadline-oriented environment
• Ability to maintain confidentiality of sensitive information
• Flexible and adapts well to change

Nice To Haves

• Master's degree preferred
• oncology clinical research experience preferred
• Knowledge of clinical research, research ethics and regulatory processes preferred

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 1,001-5,000 employees