Clinical Research Assistant I
at OHRI
Ottawa, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 29 Nov, 2024 | USD 19 Hourly | 01 Sep, 2024 | 2 year(s) or above | Harmonisation,Onedrive,Communication Skills,Training,Microsoft Teams,Management Skills,Outlook,Access,Excel,Powerpoint,Health Sciences | No | No |
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Description:
We are seeking a dynamic individual to join our team within the most active and productive emergency medicine research program in Canada. The Research Assistant will contribute to our multi-center, multi-year, and multi-facetted emergency medicine research studies. The candidate will report directly to the Principal Investigator, Dr. Venkatesh Thiruganasambandamoorthy.
BASIC REQUIREMENTS (EDUCATION/EXPERIENCE):
- Must be able to work flexible hours including some evenings and weekends.
- Candidate will be expected to travel between the Civic and General Campuses (with potential travel to Queensway Carleton Hospital and Montfort Hospital)
- Excellent interpersonal and communication skills
- Evidence of training certification in Tri-Council Policy Statement -2 (TCPS-2) and the International Conference on Harmonisation – Good Clinical Practice Guidelines (ICH-GCP)
- Evidence of training in Food and Drug Regulations, Division 5, and/or Device Regulations
- Superior organizational, analytical and time management skills
- Ability to work independently and as a team member.
- Strong communication skills and bedside manner
- Ability to set priorities and work in a dynamic environment.
- Must be proficient in basic computer software such as MS Word, Excel, Powerpoint, Outlook, OneDrive, Microsoft Teams, etc.
PREFERRED QUALIFICATIONS:
- University degree in health sciences or related field
- 2-3 years of previous experience working in a clinical research setting
- Clinical background
- Access to a car
- Bilingual
Responsibilities:
- Recruitment of study participants: Obtain consent and enroll patients into studies; coordinate follow-up appointments as necessary.
- Track study compliance, update study logs and complete study forms (CRFs, ECGs, Outcome assessment, etc.)
- Conduct telephone follow-ups.
- Assist with data collection, data entry and data cleaning.
- Help prepare reports, presentations, and manuscripts submission.
REQUIREMENT SUMMARY
Min:2.0Max:3.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Health sciences or related field
Proficient
1
Ottawa, ON, Canada