Clinical Research Coordinator Driving Patient-Centered Research Initiatives
RI-MUHC | Research Institute of the MUHC | #rimuhc • montreal (administrative region), Canada
Role Description
Join a renowned research institute as a Clinical Research Coordinator and advance your career in biomedical science. Lead clinical trials by recruiting participants and ensuring protocol adherence in a state-of-the-art facility.
This pivotal role involves responsibilities for the Centre for Innovative Medicine, focusing on maintaining ethical standards and enhancing data integrity across clinical trials. You will coordinate participant recruitment, collect relevant data, and ensure compliance with all regulatory requirements while working closely with a dedicated team.
Key Responsibilities:
• Manage the ethics approval process for clinical protocols
• Facilitate participant recruitment and informed consent
• Maintain comprehensive study documentation
• Coordinate follow-up visits and adverse event updates
• Collaborate with study monitors and the quality assurance team
Requirements:
• At least 2 years of experience in clinical research
• Educational backgr...
This pivotal role involves responsibilities for the Centre for Innovative Medicine, focusing on maintaining ethical standards and enhancing data integrity across clinical trials. You will coordinate participant recruitment, collect relevant data, and ensure compliance with all regulatory requirements while working closely with a dedicated team.
Key Responsibilities:
• Manage the ethics approval process for clinical protocols
• Facilitate participant recruitment and informed consent
• Maintain comprehensive study documentation
• Coordinate follow-up visits and adverse event updates
• Collaborate with study monitors and the quality assurance team
Requirements:
• At least 2 years of experience in clinical research
• Educational backgr...