Research Coordinator
Hamilton Health Sciences
Hamilton, ON-
Number of positions available : 1
- Salary 36.61 to 46.93 $ according to experience
- Full time
- Published on April 16th, 2025
-
Starting date : 1 position to fill as soon as possible
Description
The JCC 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 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 staff at other institutions throughout Ontario.
2. Three (3) years experience in a clinical research setting (oncology clinical research preferred)
3. Knowledge of clinical research, research ethics and regulatory processes preferred
4. Clinical Trials Research Coordinator Course (CRTC) and/or Certification as a Clinical Research Professional/Coordinator
5. 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
6. Proficient understanding of medical terminology
7. Exceptional computer skills including MS Word, Excel, and Outlook
8. Knowledgeable of electronic document management systems
9. Superior organizational, project and time management skills
10. Attention to detail is a must
11. Well-developed oral and written communication, and interpersonal skills
12. Strong analytical, critical thinking, organizational and time management skills
13. Demonstrated ability to work both independently and as part of a team
14. Ability to prioritize and work effectively in a fast-paced, deadline-oriented environment
15. Ability to maintain confidentiality of sensitive information
16. Flexible and adapts well to change
Read more
Qualifications
1. University degree in a health sciences-related field; Master's preferred 2. Three (3) years experience in a clinical research setting (oncology clinical research preferred)
3. Knowledge of clinical research, research ethics and regulatory processes preferred
4. Clinical Trials Research Coordinator Course (CRTC) and/or Certification as a Clinical Research Professional/Coordinator
5. 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
6. Proficient understanding of medical terminology
7. Exceptional computer skills including MS Word, Excel, and Outlook
8. Knowledgeable of electronic document management systems
9. Superior organizational, project and time management skills
10. Attention to detail is a must
11. Well-developed oral and written communication, and interpersonal skills
12. Strong analytical, critical thinking, organizational and time management skills
13. Demonstrated ability to work both independently and as part of a team
14. Ability to prioritize and work effectively in a fast-paced, deadline-oriented environment
15. Ability to maintain confidentiality of sensitive information
16. Flexible and adapts well to change
Requirements
Level of education
undetermined
Work experience (years)
undetermined
Written languages
undetermined
Spoken languages
undetermined
Other Hamilton Health Sciences's offers that may interest you