Clinical Research Coordinator

**Clinical Research Coordinator I (RC I)**

**Competition**:
Clinical Research Coordinator I (RC I)

**Program**:
Bruyère Research Institute

**Position Type**:
1 year contract with possibility of renewal

**Salary Scale**:
$$30.53 - $34.81/hour plus benefits

**Main duties and responsibilities**:

- Coordinate clinical trials studies in compliance with ICH GCP
- Obtain required approvals to conduct the study from study department, REB, Privacy Office and sponsor
- Organize project meetings as required and provide study progress reports to the sponsor, Principal Investigator, and study team.
- Work with the recruitment team to screen potential participants for study eligibility, including the collection and documentation of medical history, test results, medication use, etc.
- Obtain and document participant informed consent
- Coordinate logístical arrangements for study visits with participants and the study team
- Conduct study visits and collect data according to study protocol
- Administer cognitive assessments with participants both virtually and in-person
- Work with multiple online platforms to collect and enter data, and obtain study information as required
- Maintain study regulatory documentation and participant source documentation
- Monitor, document and report adverse events, serious adverse events and deviations as per study protocol, REB guidelines and Health Canada requirements.
- This job description is not exhaustive. Additional duties may be added as projects progress._

**Required Competencies**:

- Bachelor’s degree (4-year) in a relevant health science related field
- Minimum 2 years relevant experience working in a clinical research environment
- Minimum 1 year experience coordinating clinical trials, including experience with direct participant contact (screening, obtaining informed consent, conducting assessments, etc.)
- Excellent verbal and written English communication skills
- Attention to detail in ensuring compliance with study protocols
- Demonstrated ability to work well independently with mínimal supervision
- Demonstrated strong organizational, time management, and prioritization skills

**Preferred Competencies**:

- Evidence of training in Tri-Council Policy Statement (TCPS-2 Core), Good Clinical Practice (GCP) Guidelines, and Health Canada Division 5 Regulations
- Master’s degree in a relevant health-related field
- Experience working with dementia populations
- Bilingualism (French and English)

**If you are interested in this opportunity, please submit a cover letter and resume.**

Bruyère Research Institute is an equal opportunity employer and values diversity in its workplace. All qualified applicants will receive consideration for employment based on skills and experience as outlined in your CV and cover letter.

Bruyère Research Institute is committed to developing inclusive, barrier-free selection processes and work environments. If contacted regarding this competition, please advise us of any accommodation measures which may be required to enable you to be assessed in a fair and equitable manner.

We thank you for your interest in this position; however, only those chosen for an interview will be contacted.

**Coordonateur/Coordonatrice en recherche clinique**
Concours:
Coordonateur/Coordonatrice en recherche clinique

**Programme**:
Institut de recherche Bruyère

**Type de poste**:
Temps complet, 37.5 heures/semaine

**Échelle salariale**:
$30.53 - $34.81/heure avec avantages

**Tâches et responsabilités principales**:
Coordonner des essais cliniques qui respectent les lignes directrices de l’ICH GCP.

Obtenir les permissions requises auprès du département de la recherche, du comité éthique de la recherche (REB), du Bureau des informations privées et du sponsor pour conduire la recherche.

Organiser des rencontres de projets au besoin et procurer des rapports sur la progression de l’étude au sponsor, à l’Investigateur Principal et à l’équipe de recherche.

Travailler avec l’équipe de recrutement pour évaluer l’éligibilité de participants potentiels aux essais cliniques; ce qui inclut la collecte et la documentation de l’histoire médicale, de résultats et tests cliniques, de la prise de médicaments etc.

Obtenir et documenter le consentement informé du participant.

Coordonner les arrangements logistiques pour les visites avec les participants à la recherche ainsi qu’avec l’équipe de recherche clinique.

Mener les visites des essais cliniques et procéder à la collecte de données selon le protocol de recherche.

Administrer des évaluations cognitives avec les participants en personne ou de façon virtuelle.

Travailler avec multiples plateformes de collecte et d’entrée de données et obtenir de l’information liée à l’essai clinique au besoin.

Maintenir de la documentation régulatrice et les documents sources des participants.

Surveiller, documenter et rapporter les effets indésirables, les effets