Site Director
ClinLab Solutions Group, Charlottesville, VA, United States
Site Director
** Direct Hire, Permanent Role **
Monday-Thursday 8am-5pm, Friday 8am-2pm
Pay: $100k-130k
Charlottesville, VA 22911
Qualifications: - Bachelor’s degree and 5+ years of clinical research experience, or equivalent combination of education and experience. - Minimum 2 years of management experience required. - Experience in clinical research site management required.
Responsibilities: - Lead and manage overall site operations, focusing on performance, efficiency, patient safety, and compliance with protocols and regulatory standards. - Coordinate with leaders in business development, patient recruitment, finance, contracts, and quality to achieve study milestones, budget targets, and deliver quality data. - Monitor site and patient activities using performance dashboards and clinical trial systems to ensure timely and accurate execution of operational tasks. - Oversee resource allocation, site assignments, and team performance, identifying and escalating risks to study timelines, quality, or budget as needed. - Support and deliver initial and ongoing training for staff on study protocols, CRF completion, SOPs, and clinical guidelines. - Ensure adherence to SOPs, GCP, FDA regulations, and internal policies, routinely assessing compliance and identifying emerging risks. - Develop and implement corrective action plans at both site and study levels to address operational or compliance issues. - Manage site staff, including recruitment, performance appraisals, training, and resolution of operational issues, while supporting successful site operations.
Qualifications: - Bachelor’s degree and 5+ years of clinical research experience, or equivalent combination of education and experience. - Minimum 2 years of management experience required. - Experience in clinical research site management required.
Responsibilities: - Lead and manage overall site operations, focusing on performance, efficiency, patient safety, and compliance with protocols and regulatory standards. - Coordinate with leaders in business development, patient recruitment, finance, contracts, and quality to achieve study milestones, budget targets, and deliver quality data. - Monitor site and patient activities using performance dashboards and clinical trial systems to ensure timely and accurate execution of operational tasks. - Oversee resource allocation, site assignments, and team performance, identifying and escalating risks to study timelines, quality, or budget as needed. - Support and deliver initial and ongoing training for staff on study protocols, CRF completion, SOPs, and clinical guidelines. - Ensure adherence to SOPs, GCP, FDA regulations, and internal policies, routinely assessing compliance and identifying emerging risks. - Develop and implement corrective action plans at both site and study levels to address operational or compliance issues. - Manage site staff, including recruitment, performance appraisals, training, and resolution of operational issues, while supporting successful site operations.