Clinical Research Assistant Ii

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...

**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...

**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...

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...

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...

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 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...

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 - Assist with data collection, data entry and data cleaning for Clinical Trials and investigator driven studies. - Manage all aspects associated with the Ottawa Health...

The Clinical Epidemiology Program (CEP) has an immediate opening for a Research Administrative Assistant II responsible for: - Providing a broad range of clerical and administrative support duties for CEP members. Predominantly focusing on the Centre for Implementation Research (CIR), the incumbent will be expected to provide support to Drs. Justin Presseau...

Developing systematic review protocols - Screening studies and extracting relevant data for systematic reviews - Performing relevant meta-analyses, as well as risk of bias assessments - Assisting other group members with all stages of systematic reviews - Providing consultations on systematic reviews - Assisting with manuscript writing - Assisting with grant...

Developing studies to assess our prototype authenticator. - Assisting other group members with evaluations of the authenticator - Providing consultations on journalology/publication science matters - Assisting with manuscript writing - Assisting with grant preparation and submissions **Basic Requirements (Education/Experience)**: - Minimum of 2 years of...

Your responsibilities will be to support multiple clinical trial operations including recruitment and consent, maintain data in online databases, perform study outcome assessments, interact with patients and clinicians, protect patient confidentiality, and perform other administrative tasks as necessary. **Basic Requirements (Education/Experience)**: -...

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...

**Basic Requirements (Education/Experience)**: - Minimum of 2 years of experience in a health research environment - Secondary school diploma in a related field - Excellent organizational skills - Strong time management skills and ability to effectively prioritize multiple projects. - Computer literacy, including proficiency in Microsoft Word, Excel,...

**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...

**Tasks may include**: - Attending meetings for patient identification and tracking - Informed consent discussions with potential participants - Chart review for data extraction and data entry - Management of database integrity and cleaning - Patient follow-ups for response assessment and treatment outcomes and update database regularly - Quarterly report...

**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...