Clinical Research Assistant I

at  OHRI

Ottawa, ON, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate29 Nov, 2024USD 19 Hourly01 Sep, 20242 year(s) or aboveHarmonisation,Onedrive,Communication Skills,Training,Microsoft Teams,Management Skills,Outlook,Access,Excel,Powerpoint,Health SciencesNoNo
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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