Senior Clinical Research Coordinator
4 days ago
We are seeking a highly skilled and experienced Sr. Clinical Research Coordinator to join our team at Medix™. As a key member of our research team, you will be responsible for the overall management of clinical trials and research studies.
Key Responsibilities:
- Study Coordination: Oversee the implementation and daily management of clinical trials, including subject recruitment, regulatory compliance, data collection, and study documentation.
- Regulatory Compliance: Ensure adherence to all regulatory requirements, including Institutional Review Board (IRB) submissions and approvals, and prepare and submit regulatory documents as required.
- Subject Recruitment and Management: Identify, recruit, and screen potential study subjects, obtain informed consent, and monitor subject progress.
- Data Management: Ensure accurate and timely data collection, entry, and reporting, and maintain and manage study databases and electronic data capture systems.
- Team Leadership and Training: Supervise and mentor junior CRCs, provide training on study protocols and regulatory requirements, and coordinate with other departments and external stakeholders.
- Study Documentation and Reporting: Prepare and review study reports, publications, and presentations, and maintain comprehensive and organized study files and records.
- Budget and Resource Management: Assist in the preparation and management of study budgets and financial reports, and monitor study expenses.
- Continuous Improvement: Stay updated with the latest developments in clinical research and regulatory guidelines, and implement process improvements and best practices to enhance study efficiency and quality.
Requirements:
- Experience in clinical research coordination and management.
- Strong knowledge of regulatory requirements and Good Clinical Practice (GCP).
- Excellent communication and leadership skills.
- Ability to work independently and as part of a team.
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Senior Clinical Research Coordinator
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Charleston, West Virginia, United States Medix™ Full timeSenior Clinical Research CoordinatorMedix™ is seeking a highly skilled and experienced Senior Clinical Research Coordinator to join our team. As a key member of our research team, you will be responsible for the overall management of clinical trials and research studies.Key Responsibilities:Oversee the implementation and daily management of clinical...
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Charleston, West Virginia, United States Medix™ Full timeJob SummaryThe Senior Clinical Research Coordinator is responsible for the overall management of clinical trials and research studies at Medix™. This role involves coordinating and overseeing all aspects of clinical research, including subject recruitment, regulatory compliance, data collection, and study documentation.Key ResponsibilitiesStudy...
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