Research Coordinator
- Hamilton, ON, Canada
Full-time
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Job details
- Job type
- Full-time
- Apply by
- Posting language
- English
- Posted
Original job description
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.
- University degree in a health sciences-related field;Master's preferred\
- 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
More about this job
Responsibilities
The Trial Activation Coordinator provides administrative support to facilitate the efficient activation of new clinical trials. They are responsible for coordinating the study activation process and ensuring quality assurance oversight within the department.
Requirements
Candidates must have a university degree in a health sciences-related field and at least three years of experience in a clinical research setting. Proficiency in clinical research regulations, medical terminology, and strong organizational skills are essential for this role.
Skills
- Clinical research
- Regulatory compliance
- Project management
- Time management
- Medical terminology
- Quality assurance
- Administrative support
- Communication
- Interpersonal skills
- Analytical skills
- Critical thinking
- MS Word
- MS Excel
- MS Outlook
- Attention to detail
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Science & Research
- Administrative
Keywords
- Clinical Trials
- Oncology
- Research Ethics
- Regulatory Processes
- Good Clinical Practice
- ICH
- Health Canada
- FDA
- OHRP
- Privacy Legislation
- Tri-Council Policy Statement
- Clinical Research Professional
- Study Activation
- Quality Assurance
- Administrative Support
- Medical Terminology
- Document Management
- Project Management
- Time Management
- Analytical Skills
- Critical Thinking
- Interpersonal Skills
- Communication
- MS Word
- MS Excel
- MS Outlook
- Health Sciences
- Clinical Research Coordinator
- Juravinski Cancer Centre