Clinical Research Assistant

1 week ago

Montréal, Canada Lady Davis Institute - Jewish General Hospital Full time

**POSITION AVAILABLE**: Clinical Research Assistant

**JOB DESCRIPTION**:
The primary responsibilities of this position are:

- Contribute to cardiovascular clinical research studies by screening, recruiting and enrolling patients;
- Plan and execute research projects;
- Participate in the preparation, conceptualization and writing of grant submissions, study protocol development, manuscripts and reports, and presentations;
- Act as a resource and provide mentorship to junior trainees on the research team;
- Collaborate with research team members and trial investigators; and
- Perform various administrative tasks including CV management, preparing PowerPoint presentations, organizing meetings, and submitting manuscripts to journals.

**QUALIFICATIONS**:

- Bilingual: French and English
- Master’s degree in epidemiology, public health, or a related field
- Detail-oriented person with the ability to collect, compile, and analyze information
- Familiarity with Good Clinical Practice is an asset
- Prior experience conducting statistical analyses is an asset
- Prior experience with systematic reviews, meta-analyses, and/or clinical trials is an asset
- Ability to work independently and as a member of a team
- Ability to work under pressure, and ability to prioritize, multi-task, and manage multiple complex projects in a fast-paced work environment
- Project management skills - ability to manage a variety of concurrent projects with mínimal supervision; problem solving and decision-making skills

**CONTACT INFORMATION**:
Mark J. Eisenberg, MD MPH

c/o Tabitha Finch, PhD

**POSTE DISPONIBLE**: Assistant(e) de recherche clinique

**DESCRIPTION DE L'EMPLOI**:
Les principales responsabilités de ce poste sont les suivantes:

- Contribuer à des études de recherche clinique cardiovasculaire en dépistant, recrutant et inscrivant des patients ;
- Fournir des soins aux sujets et des procédures de collecte de données dans le respect du protocole d'étude et conformément aux bons principes de recherche clinique ;
- Recueillir des informations et des données pertinentes à partir des dossiers et registres des sujets, des entretiens avec des sujets et d'autres sources. Remplir les formulaires de rapport de cas (CRF) conformément aux lignes directrices du protocole de recherche ;
- Planifier et exécuter des projets de recherche ;
- Participer à la préparation, à la conceptualisation et à la rédaction des demandes de subventions, à l'élaboration des protocoles d'étude, aux manuscrits et aux rapports, ainsi qu’aux présentations ;
- Agir à titre de ressource et de mentor auprès des jeunes stagiaires de l'équipe de recherche ;
- Collaborer avec les membres de l'équipe de recherche et les investigateurs des essais ; et
- Effectuer diverses tâches administratives dont la gestion des CV, la préparation de présentations PowerPoint, l'organisation de réunions et la soumission de manuscrits à des revues.

**QUALIFICATIONS**:

- Bilingue : français et anglais
- Maîtrise en épidémiologie, en santé publique ou dans un domaine connexe
- Excellentes compétences rédactionnelles en anglais (par exemple, publications en tant que premier auteur, soumissions de demandes de subventions)
- Personne soucieuse du détail, capable de recueillir, de compiler et d’analyser des informations
- Une bonne connaissance des Bonnes pratiques cliniques (BPC) est un atout
- Une expérience préalable dans la réalisation d'analyses statistiques est un atout
- Une expérience préalable des revues systématiques, des méta-analyses et / ou des essais cliniques est un atout
- Capacité à travailler de manière indépendante, et en tant que membre d’une équipe
- Capacité à travailler sous pression, à établir des priorités, à mener plusieurs tâches de front et à gérer plusieurs projets complexes dans un environnement de travail en constante évolution
- Compétences en matière de gestion de projet - capacité à gérer une variété de projets simultanés avec une supervision mínimale ; compétences en matière de résolution de problèmes et de prise de décision

**COORDONNÉES**:
Mark J. Eisenberg, MD MPH

c/o Tabitha Finch, PhD

**Job Types**: Full-time, Permanent

**Salary**: $23.00-$25.00 per hour

**Benefits**:

- Casual dress
- Company pension
- Dental care
- Disability insurance
- Extended health care
- Flexible schedule
- Life insurance
- Paid time off
- RRSP match
- Vision care

Schedule:

- 8 hour shift
- Day shift

COVID-19 considerations:
Ability to commute/relocate:

- Montréal, QC H3T 1E2: reliably commute or plan to relocate before starting work (preferred)

**Education**:

- Master's Degree (preferred)

**Language**:

- French (preferred)
- English (preferred)

Work Location: In person

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