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Project Manager for Clinical Trials
Job Description & How to Apply Below
As a key player in the MIST Trial, you will supervise the trial's infrastructure and regulatory compliance. With your previous experience in multi-centre trials, you'll facilitate effective communication with international research sites. Your skills in project management will ensure timely reporting and tracking of enrolled patients and related finances.
Key Responsibilities:
• Coordinate management of the multi-centre MIST Trial
• Ensure adherence to regulatory guidelines across sites
• Maintain and update the Trial Master File
• Monitor site-level budgets and invoicing
• Organize meetings and track action items effectively
Requirements:
• 3+ years in clinical research settings
• Bachelor of Science or equivalent
• Certified in TCPS-2 and ICH-GCP guidelines
• Training in relevant regulations
• Excellent organizational skills
Utilize your expertise to enhance patient recovery and quality of life in innovative cardiac treatments.
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