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Research Associate

1 month ago

Ottawa, Ontario, Canada CHEO Full time
Job Title: Research Associate

We are seeking a highly motivated and experienced Research Associate to join our team at the CHEO Research Institute. The successful candidate will be responsible for participating in grant writing, drafting manuscripts, and managing administrative responsibilities of the research department, including human resources.

Responsibilities:
  • Grant writing and manuscript writing: The Research Associate will be responsible for drafting grant applications and manuscripts from A to Z, using general bullet points provided by the supervisor.
  • Human Resources: The Research Associate will be responsible for renewing or terminating employee contracts, timekeeping and tracking employee absences, promoting an integrated research team, and providing assistance and mentoring to research staff.
  • Program Growth and Development: The Research Associate will be responsible for developing new study budgets, coordinating contract execution, and leading or assisting with establishing enrolment strategies.
  • Financial Management: The Research Associate will be responsible for assisting in the development of study budgets, monitoring and managing research accounts within budgets, overseeing payments and revenue for studies, and monitoring the overall research funding envelope.
  • Health Canada Regulated studies: The Research Associate will be responsible for leading clinical trials and submitting applications to Health Canada for regulated studies.
Qualifications:
  • Master's degree in a social science/education/health field and/or equivalent field (Essential)
  • PhD degree (Preferred)
  • Experience with writing grants for CIHR or NIH (Essential)
  • Published at least 5 manuscripts as first or last author (Essential)
  • Experience with Health Canada regulated clinical trials (Essential)
  • Minimum 3 years clinical research experience (Essential)
  • Understanding of research design, procedures, guidelines and standards governing clinical research (Essential)
  • Outstanding writing skills (Essential)
  • Experience with clinical trials registration (Essential)
  • Data management experience (Essential)
  • Statistical skills (descriptive statistics, modeling and more) (Essential)
Working Conditions:
  • Flexibility to work remotely in a hybrid work model that would include both remote work and on-site work
  • Able to be flexible with working hours to help meet deadlines
  • Able to work under tight deadlines
  • Able to work in a team as well as independently under sometimes very minimal supervision
Other Requirements:
  • Eligible to work in Canada;
  • Compliance with CHEO RI's Universal COVID-19 Vaccination Policy; and
  • Police Record Check

To apply, please send a complete CV and cover letter to Dr. Robinson at Researchhr@cheo.on.ca.