Clinical Trials Coordinator
2 weeks ago
Job Title: Clinical Trials Coordinator
Welcome to Medix™, where we are seeking a committed Clinical Trials Coordinator to enhance our research initiatives.
Overview:
In this position, you will be responsible for ensuring that sanctioned protocols are accurately executed and adhered to. Your duties will include managing the informed consent process, overseeing patient safety and status, gathering and organizing research data, and delivering study-specific training to both staff and participants. The Clinical Trials Coordinator should also possess the ability to perform a variety of clinical functions.
Key Responsibilities:
- Preparation of study sites
- Securing informed consent, screening, and recruiting patients
- Enrollment of participants and conducting study visits
- Managing and distributing study-related products and supplies
- Completing and ensuring the integrity of case report forms
- Maintaining source documentation
- Ensuring quality at the study site
- Possessing a comprehensive understanding of protocol requirements and schemas
- Collaborating with medical professionals to uphold protocol compliance
- Drafting patient information materials for clinical study submissions
- Contributing to the development of educational resources for patients
- Reviewing research and administrative documentation
- Overseeing the completion and submission of regulatory documents
- Managing research funding accounts, budgets, and financial transfers
- Responding to inquiries, data requests, and informational needs
- Analyzing statistical, resource, performance, and budgetary data
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