Job Description: Regional Site Director
The Company
Are you an ambitious and proactive individual seeking an exciting opportunity in clinical research? Join Axsendo Clinical Research, a rapidly growing network of clinical research sites specializing in Neurology, Cardiology, Metabolic Disease, Vaccines and Medical Devices. We are eager to welcome a dedicated Regional Site Director to contribute to our dynamic and busy team!
The Role
Clinical Site Management
- Supervise day-to-day operations at clinical trial sites, ensuring adherence to protocols, guidelines, and regulations.
Coordinate site activities, including participant recruitment, data collection, and study procedures, to meet project timelines.
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Compliance and Quality Assurance
- Ensure strict adherence to regulatory standards, ethical practices, and study protocols.
Conduct regular site audits to maintain compliance with applicable regulations and quality standards.
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Stakeholder Coordination:
- Collaborate with principal investigators, sponsors, and ethics committees to facilitate communication and resolve site-related issues promptly.
Act as the primary point of contact between the site and sponsors, providing updates on study progress and addressing queries.
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Resource Management:
- Manage site resources effectively, including staff, equipment, and supplies, to support smooth trial operations.
- Optimize resource allocation to ensure efficient utilization and cost-effectiveness.
- Training and Development:
- Provide training to site staff on study protocols, procedures, and regulatory requirements.
Foster a culture of continuous learning and skill development among site personnel.
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Data Management:
- Oversee accurate and timely data collection, ensuring data integrity and quality control measures are in place.
Collaborate with data management teams to resolve data discrepancies and maintain data accuracy.
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Qualifications:
- Bachelor’s degree in a relevant field (master’s preferred) and a minimum of 5 years of experience in clinical research site management.
- In-depth knowledge of clinical trial operations, regulations, and ethical guidelines.
- Strong leadership and interpersonal skills, with the ability to manage diverse teams and stakeholders effectively.
- Excellent problem-solving abilities and attention to detail.
- Proficiency in clinical trial management software and data management systems