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    Regional Site Director - Houston, United States - Axsendo Clinical

    Axsendo Clinical
    Axsendo Clinical Houston, United States

    2 weeks ago

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    Description

    Job Description

    Job DescriptionSalary: $85,000-115,000

    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.

    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:

    • 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
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