National Clinical Research Coordinator

Research Project  

Randomised pilot study of an e-intervention aimed at reducing the harms of cannabis use (CHAMPS) for young adults with early psychosis who use cannabis 2.0

The primary objective of this Canadian multi-site trial is to determine whether adding an app-based harm reduction intervention (CHAMPS) to early intervention services for psychosis reduces cannabis-related problems among young people with psychosis. Secondary objectives include assessing the effect of CHAMPS on motivation to change protective behaviours related to cannabis, cannabis use patterns, cannabis use, quality of life, satisfaction with treatment, and healthcare utilisation.

 

Responsabilities

As National Clinical Research Coordinator, you will be responsible for:

  • Coordinating protocol-related activities in collaboration with our internal and external partners
  • Coordinating the work organisation of research team members involved in the protocol
  • Approaching participants for consent and enrolling them in the study
  • Collecting and entering data
  • Following up with participants enrolled in the study
  • Ensuring ethical and regulatory compliance in accordance with GCP and CHUM research standards (NAGANO)
  • Contribute to ethical approval applications and contract reviews
  • And any other tasks related to the research group

 

Qualifications

  • SOCRA Certified Clinical Research Professional certification or equivalent certification related to the responsibilities of the position
  • Minimum of 5 years of experience in clinical research or experience relevant to this role
  • Undergraduate degree in humanities or a field relevant
  • Knowledge of public health and/or qualitative research is an asset
  • Bilingualism (French/English) spoken and written
  • Excellent command of office software (Word, Excel, PowerPoint)
  • Sense of responsibility, good judgement, autonomy, proactivity
  • Ability to work in a team and manage multiple files at once
  • Demonstrate excellent priority management in a rapidly changing environment
  • Experience in clinical research and knowledge of good clinical practices

 

Status and advantages

  • Part-time position, 3 days per week or 21 hours per week
  • Flexible schedule and work from home possible
  • Start date: as soon as possible
  • One-year contract, renewable
  • Possiblity of full-time work if desired
  • Salary range between 30.27$ et 53.64$ per hour
  • 8% vacation pay accrued on a pro rata basis for time worked from 1 May to 30 April
  • The following fringe benefits are available to part-time employees: 5.7% financial compensation for public holidays and 4.21% financial compensation for sick days
  • Pension plan (RREGOP) from the first day of employment
  • Group insurance

 

To apply

Interested candidates should send their CV and cover letter to: jane.marie.ramil.chum@ssss.gouv.qc.ca

Only candidates selected for an interview will be contacted. The CRCHUM encourages women, Indigenous peoples, visible minorities, ethnic minorities, and persons with disabilities to apply. The CRCHUM adopts a broad and inclusive definition of diversity that goes beyond applicable laws. The CRCHUM therefore encourages all individuals, regardless of their characteristics, to apply. In accordance with Canadian immigration requirements, please note that priority will be given to Canadian citizens and permanent residents.