Support a prestigious Diabetes study as a Clinical Research Coordinator with a hybrid work model. This role offers 40 hours per week on a 7-month contract basis.

As a Clinical Research Coordinator, you will ensure compliance with relevant regulations while coordinating study activities from initiation to closure. Working closely with research staff, you will organize and maintain clinical data, making significant contributions to the study. Applicants must be local to the area and prepared for intensive, results-driven work.

Key Responsibilities:
• Manage data collection and organize source documentation
• Screen potential participants for clinical trial eligibility
• Maintain accurate records in electronic data systems




• Conduct site qualification and initiation visits
• Trigger financial payments and oversee study close-out

Requirements:
• Must reside within a 1-hour commuting distance
• Familiarity with IRB documents and regulatory submissions
• Proficiency in electronic data capture systems
• Solid data management and analytical skills
• Commitment to a 40-hour hybrid workweek

Utilize your clinical research skills to enhance diabetes treatment research with a respected sponsor.
#J-18808-Ljbffr

📌 Clinical Research Coordinator for Diabetes Study (British Columbia)
🏢 Medix™
📍 British Columbia