Clinical Research Coordinator Ii

Aventiv Research, IACT Health, LMC Manna Research, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as Aventiv operate in Ohio and Arizona and specialize in phase 1 pharmaceutical, device, and diagnostic...

Aventiv Research, IACT Health, LMC Manna Research, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as Aventiv operate in Ohio and Arizona and specialize in phase 1 pharmaceutical, device, and diagnostic...

**Clinical Research Coordinator I (RC I)** **Competition**: Clinical Research Coordinator I (RC I) **Program**: Bruyère Research Institute **Position Type**: 1 year contract with possibility of renewal **Salary Scale**: $$30.53 - $34.81/hour plus benefits **Main duties and responsibilities**: - Coordinate clinical trials studies in compliance with ICH...

The Division of Orthopaedic Surgery is seeking a full-time Clinical Research Assistant II for a one-year contract who will be based at the Civic Campus. This is position is a temporary maternity leave coverage. The individual will be responsible for patient recruitment, data collection, data entry, and ethics submissions for a multitude of ongoing clinical...

The Clinical Study Associate (CSA) is an integral part of the study team, responsible for the creation, distribution and quality of clinical trial materials, tools and documents. The position supports the Clinical Study Manager and Data Management by tracking and reporting study metrics as well as by performing in-house office administrative activities to...

Aventiv Research, IACT Health, LMC Manna Research, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as Aventiv operate in Ohio and Arizona and specialize in phase 1 pharmaceutical, device, and diagnostic...

The Clinical Study Associate (CSA) is an integral part of the study team, responsible for the creation, distribution and quality of clinical trial materials, tools and documents. The position supports the Clinical Study Manager and Data Management by tracking and reporting study metrics as well as by performing in-house office administrative activities to...

**Responsibilities for this position include, but are not limited to**: - Screen patients, obtain consent and enroll participants into studies, coordinate follow-up appointments as necessary - Track study compliance, update study logs and complete study forms - Conduct telephone follow-ups - Assist with data collection, data entry and data cleaning - Help...

The Psychosocial Oncology Program at The Ottawa Hospital Cancer Centre is seeking a skilled Clinical Research Assistant II to assist with a project focused on better understanding the psychological experience of individuals with advanced cancer who are receiving immunotherapy or targeted therapy, and other related projects. Important responsibilities...

Dr. Daniel McIsaac is an anesthesiologist and scientist at The Ottawa Hospital and a CIHR-funded investigator. As team lead for the Aging Innovation in Perioperative Medicine & Surgery (AIMS) Research Group, Dr. McIsaac’s research program at the Ottawa Hospital Research Institute looks to improve the care and outcomes of older people who require major...

**Basic Requirements (Education/Experience)**: - Secondary school diploma - 2 years of clinical research experience. - Evidence of training certification in Tri-Council Policy Statement -2 (TCPS-2) and the International Conference on Harmonization - Good Clinical Practice Guidelines (ICH-GCP). - Proven ability to carry out the tasks required for clinical...

**Basic Requirements (Education/Experience)**: - 2 years of clinical research experience - Secondary school diploma - Evidence of training certification in Tri-Council Policy Statement -2 (TCPS-2) and the International Conference on Harmonization - Good Clinical Practice Guidelines (ICH-GCP) - Proven ability to carry out the tasks required for clinical...

The Clinical Investigation Unit (CIU) is looking for an experienced Clinical Research Assistant II to collaborate with investigators and the CIU team to assist with the research administration of clinical studies. The CIU is a 12-bed clinical research facility with an integrated Pharmacokinetics (PK) Lab located at the General Campus of The Ottawa Hospital....

Dr. Angela Cheung of the OHRI is seeking an experienced Clinical Research Assistant II to join the Clinical Epidemiology program. **Responsibilities will include**: **Basic Requirements (Education/Experience)**: - A bachelor’s degree in a health science-related field - 2 years’ experience in a clinical research environment - Evidence of training in...

Dr. Daniel McIsaac is an anesthesiologist and scientist at The Ottawa Hospital and a CIHR-funded investigator. As team lead for the Aging Innovation in Perioperative Medicine & Surgery (AIMS) Research Group, Dr. McIsaac’s research program at the Ottawa Hospital Research Institute looks to improve the care and outcomes of older people who require major...

The Clinical Investigation Unit (CIU) is looking for an experienced Clinical Research Assistant II to collaborate with investigators and the CIU team to assist with the research administration of clinical studies, especially the ethics review process. The CIU is a 12-bed clinical research facility located at the General Campus of The Ottawa...

**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...

We are recruiting for a Clinical Research Assistant II who will manage and maintain the C3 Registry on REDCap. This will include requesting and reviewing medical records from hospitals for C3 patient members and extracting relevant data to add to the C3 Registry. In addition, the current state of the Registry will be transitioning to a new platform (“the...

**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,...