Clinical Research Assistant I

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...

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...

**Position Information** **Posting Number**: - IMHR24-008E**Title**: - Research Assistant I (TFT 1.0FTE)**Position Status**: - Temporary Full-time**Contract End Date**: - 09/26/2025**FTE**: - 1.0**Job Schedule**: - Days**Department**: - IMHR**Union**: - Non-union**Site**: - Institute of Mental Health Research (IMHR)**About The Royal** As one of...

Assisting with the development of study protocols, surveys and interview guides - Screening studies and extracting relevant data for systematic reviews - Assisting with interview and survey studies - Co-developing patient engagement strategies and coordinating engagement - Designing and facilitating educational workshops and resources - Assisting with...

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...

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...

**The responsibilities include**: - Cognitive testing, data collection, data entry, database management and assistance with statistical analyses, where appropriate - Scheduling and consenting patients for research studies - Providing clerical and administrative support for the NCTS as needed - Providing general assistance in the day-to-day management of the...

**Position Information** **Posting Number**: - IMHR24-009E**Title**: - Research Coordinator I (TFT 1.0 FTE)**Position Status**: - Temporary Full-time**Contract End Date**: - 11/14/2025**FTE**: - 1.0**Job Schedule**: - Days**Department**: - IMHR**Union**: - Non-union**Site**: - Institute of Mental Health Research (IMHR)**About The Royal** - As one...

**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,...

**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...

Assisting with study protocols, - Assisting with screening studies and extracting relevant data for systematic reviews - Assisting with ongoing preclinical and clinical studies - Assisting with manuscript writing and submissions - Assisting with grant preparation **Basic Requirements (Education/Experience)**: - A secondary diploma - Clinical research...

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....

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...

Projects in maternal-newborn care. The Clinical Research Assistant (CRA III) will assist in protocol and procedure manual development, database and case report form development, research ethics board submissions, assistance with regulatory and administrative management of clinical trials and other research projects. The (CRA III) will facilitate the conduct...

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...

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 OMNI Research Group is seeking a highly motivated individual to work with a variety of clinical trials and research projects in maternal-newborn care, and women’s health. The Clinical Research Assistant (CRA) will participate in research ethics board submissions, renewals, regulatory and administrative management of studies, maintaining project day to...

The Department of Radiology is seeking a highly motivated individual to assist with various research projects. Under the supervision of the Senior Clinical Research Program Manager, the Clinical Research Assistant III will work primarily on research ethics documents including full board REB submissions, renewals, amendments, and terminations of research...