What are the responsibilities and job description for the Clinical Site Director position at Axsendo Clinical?
Job Description
Job Description
Salary : $72,000-109,000 / Year
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 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.
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.
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.
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.
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.
Qualifications :
Bachelors degree in a relevant field (masters 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
Highlights
Health insurance benefit eligibility after 90 days
Great company culture and tons of room for growth!
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