Clinical Research Nurse Coordinator (Research Institute)

Research Institute of the McGill University Health Centre; Montreal; On-site; CAD 50,000 - 70,000; Full time

Job summary

The Research Institute of the McGill University Health Centre is hiring a clinical research assistant focused on inflammatory bowel disease (IBD). This role involves patient follow-up in clinical trials, data management, and collaboration with physicians and nurses. Candidates should be bilingual and possess a DEC in Nursing.

Qualifications

• Experience in research is considered an asset.
• OIIQ certification is a plus.
• Ability to work independently and within a team.

Responsibilities

• Follow-up of patients in clinical trials including administration of study drugs.
• Process and prepare biological samples for international shipment.
• Assist Senior research staff with ethics and regulatory tasks.

Skills

Time management

Organizational skills

Proactivity

Communication skills

Interpersonal skills

Bilingual (French and English)

Education

Diploma of College Studies (DEC) in Nursing

Job description

Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the McGill University Health Centre (RI-MUHC), you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and make a difference!

Job Description

RESEARCH INSTITUTE OF THE MUHC

The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research centre. Located in Montreal, Quebec, the Institute is the research arm of the McGill University Health Centre (MUHC) affiliated with the Faculty of Medicine at McGill University. The RI-MUHC is supported in part by the Fonds de recherche du Québec - Santé (FRQS).

Position summary

The incumbent will be involved with clinical research in gastroenterology and more specifically inflammatory bowel disease (IBD). Document and data management is an essential part of this position. The incumbent will work closely with research team, IBD physicians as well as with gastroenterology nurses mainly on clinical study protocols.

The person will also help to initiate industry sponsored clinical trials including assisting with REB documents, coordination, regulatory work, advertising, and accounting.

General Duties

• Follow-up of patients included in clinical trials, including administration of study drugs and care coordination,
• Processes and prepares biological samples for international shipment,
• Completes source documents and electronic case report forms,
• Identify potential patients and obtain their consent,
• Completes and maintains up-to-date specific trainings,
• Collaborates and assists team members and sponsors’ representatives,
• Reviews study protocols and informed consent forms,
• Contacts patients and their families as needed,
• Screens and collects medical charts of eligible patients,
• Assists Senior research staff with the ethics and regulatory tasks,
• Completes of all other connected tasks as assigned by supervisor,
• Complies with Good clinical practice standards (GCP).

STANDARDS OF PERFORMANCE :

• Good time management, and organizational skills are a must,
• Autonomy and proactivity,
• Ability to take initiative and resourcefulness
• Ability to multitask,
• Good listening, good interpersonal and communication skills,
• Respect of policies and procedures,

Website of the organization

Education / Experience

Diploma of College Studies (DEC)

Field of Study : Nursing

Work Experience : Experience in research will be considered an asset

If yes, please specify : OIIQ

Other Requirements :

• Excellent French and English, spoken and written,
• Excellent communication and interpersonal skills,
• Ability to work independently and in team with minimum supervision.