Clinical Research Coordinator

IACT Health, LMC Manna Research, and True North Clinical Research joined forces in late 2021 to become Centricity Research. Centricity Research is a clinical research organization with more than 40 sites, access to over 1.6 million patients, and more than 150 active investigators across Canada and the southeastern United States. Our name, Centricity...

The Ottawa Hospital Research Institute is the research arm of The Ottawa Hospital  – one of Canada’s largest learning and research hospitals. We are proudly affiliated with the University of Ottawa and supported by The Ottawa Hospital Foundation. With more than 2200 scientists, clinician investigators, trainees and staff, and total revenues of more...

The Division of Gastroenterology seeks an experienced Clinical Research Coordinator to assist with coordination and administration of investigator-initiated research studies conducted by division members. Tasks include, but are not limited to, REB submissions, contracts procurement, coordinating the day-to-day operations of studies, overseeing patient...

The IBD Centre of Excellence within the Division of Gastroenterology seeks an experienced clinical research coordinator to assist with coordination and administration of industry-led trials and investigator-initiated research. Tasks include, but are not limited to, REB submissions, contracts procurement, coordinating the day-to-day operations of studies,...

The HIV research group at The Ottawa Hospital is looking for a Clinical Research Coordinator who along with other members of the research team will be responsible for the day-to-day operations of a number of both industry sponsored, and investigator initiated clinical trials. postsecondary degree or diploma **Basic Requirements (Education/Experience)**: -...

The HIV research group at The Ottawa Hospital is looking for an enthusiastic individual to join the team as a Clinical Research Coordinator. Along with other members of the research team, the individual will be responsible for the day-to-day operations of a number of both industry sponsored, and investigator initiated clinical trials. **Basic Requirements...

Dr. Cheung is also keenly interested in leveraging artificial intelligence to improve patient care. Finally, our team works closely with patient and caregiver partners to ensure that research design, implementation and translation meet the needs of the ultimate beneficiaries of our research. There will thus be an opportunity to work with a wide range of...

Dr. Cheung is also keenly interested in leveraging artificial intelligence to improve patient care. Finally, our team works closely with patient and caregiver partners to ensure that research design, implementation and translation meet the needs of the ultimate beneficiaries of our research. There will thus be an opportunity to work with a wide range of...

About The Ottawa Hospital Research InstituteThe Ottawa Hospital Research Institute is the research arm of The Ottawa Hospital, one of Canada's largest learning and research hospitals. We are proudly affiliated with the University of Ottawa and supported by The Ottawa Hospital Foundation. Our research spans more than a hundred different diseases, conditions,...

**Tasks may include**: - Patient recruitment and follow-up, data collection and data entry - Overseeing study start-up activities (approvals, contract, regulatory documents, training) internally for investigator-initiated trials - Maintaining current up-to-date regulatory binder/files - Facilitating physician oversight over study participants following GCP...

**Posted date** - Thursday, October 31, 2024**Deadline** - Thursday, November 21, 2024**Start date** - As soon as possible**Job type** - Contract**Work hours** - Full-Time**Competition number** - ATF2448**Salary** - Commensurate with experience**Number of vacancies** - 1**Unit/Department** - Clinical Research - CardiologyTerm Two-year...

**Start date**: As soon as possible. **Term**: One-year contract. **Responsibilities**: - Coordinate and implement investigator initiated, low to moderate risk clinical, research protocols. - Monitors the ongoing clinical status of patients, assessing for adverse events while they are receiving study interventions - Prepare and maintain patient research...

**Start date**: As soon as possible. **Responsibilities**: - Coordinate and implement investigator initiated, low to high risk clinical research protocols. - Lead the implementation of multi centre or larger complex clinical research projects. - Monitors the ongoing clinical status of patients, assessing for adverse events while they are receiving study...

**Start date**: As soon as possible. **Responsibilities**: - Coordinate and implement investigator initiated, low to moderate risk clinical, research protocols. - Provide support to clinical research nurse coordinator in the implementation of multi centre or larger complex clinical research projects. - Monitors the ongoing clinical status of patients,...

**Position Information** **Posting Number**: - AI24-002E**Title**: - Clinical Research Coordinator/Coordonnatrice ou coordonnateur de recherche clinique**Position Status**: - Regular Full-time**FTE**: - 1.0**Job Schedule**: - Days**Department**: - Atlas Institute for Veterans and Families**Union**: - Non-union**Site**: - Atlas Institute for Veterans...

Unlock the Potential of Mental Health ResearchThe Royal Mental Health Centre is committed to advancing interventional repetitive Transcranial Magnetic Stimulation (rTMS) treatment strategies for clients diagnosed with difficult-to-treat mood disorders. As a Research Coordinator I, you will play a crucial role in supporting the Neuromodulation Research clinic...

The Clinical Research Navigator and Quality Coordinator will act as the primary liaison between investigators, research staff, and relevant stakeholders at OHRI, to help navigate the regulatory and logístical aspects of the conduct of research at the OHRI. The responsibilities include engaging with investigators early in their appointment and project...

Conducting and overseeing various aspects of the Blueprint group, including: - Project management for the Blueprint research team - Preparing any required Research Ethics Board submissions - Preparing and maintaining budgets and/or timelines for funded and unfunded projects - Developing study protocols, surveys, and interview guides - Co-developing patient...

The Division of Orthopaedic Surgery is seeking a part-time (20 hrs/week) Clinical Research Assistant I for a 6-month contract, with the possibility of extension. The individual will primarily be responsible for patient recruitment and follow-up, data collection, and data entry, for a multitude of ongoing clinical research trials under the general direction...

**Basic Requirements (Education/Experience)**: - Bachelor’s degree or certificate in health sciences or related field (e.g., RN or PT etc.) - 2 year of previous clinical research experience - A comprehensive understanding of the clinical research process - Evidence of training in Tri-Council Policy Statement 2 (TCPS2), the international conference of...