Associate Director, Clinical Research (U.S. Remote)
MICROVENTION, INC.
Lead the strategic planning and operational execution of clinical trials within the neurovascular therapeutic area. Responsible for driving clinical program success through effective study management, team leadership, and strong cross-functional collaboration with Medical Affairs, PACE, Regulatory, Clinical Safety, and Data Management. Ensure high standards of patient safety, data quality, and regulatory compliance while supporting the development and growth of the clinical research team. Job duties:
Operational LeadershipLead and manage Clinical Operations teams to ensure effective study execution, protocol compliance, timelines, and budget adherence. Oversee clinical site management activities including selection, initiation, monitoring, and close-out with strong regulatory and GCP compliance. Collaborate with Medical Affairs, Clinical Quality Assurance, Clinical Data Management and Clinical Safety functions to maintain data integrity and timely safety reporting. Identify and resolve operational challenges proactively to ensure project success.Strategic Support & CollaborationAssist in developing and implementing clinical trial strategies aligned with business priorities.Act as a key liaison between Clinical Operations and departments such as Regulatory Affairs, Quality, R&D, PACE, R&D, and Medical Affairs to ensure alignment and smooth communication. Manage vendor relationships and CRO oversight to meet quality standards and timelines.People Management & Team DevelopmentSupervise, mentor, and develop Clinical Operations staff to build a high-performing and engaged team. Drive performance management, goal setting, and professional growth initiatives within the team. Foster a culture of collaboration, accountability, and continuous improvement.Project ManagementDevelop and monitor project plans, resource allocation, and budgets for clinical trials. Provide regular status updates to senior leadership and escalate risks appropriately. Facilitate effective cross-functional team meetings and communication.Compliance & Quality AssuranceEnsure compliance with applicable regulatory requirements, company policies, and SOPs2. Prepare for and support audits and inspections; lead corrective and preventive actions as needed. Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization. Perform additional duties as assigned.Salary Range:
$158,000 - $195,000 Financial compensation packages may be higher/lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demands,
Operational LeadershipLead and manage Clinical Operations teams to ensure effective study execution, protocol compliance, timelines, and budget adherence. Oversee clinical site management activities including selection, initiation, monitoring, and close-out with strong regulatory and GCP compliance. Collaborate with Medical Affairs, Clinical Quality Assurance, Clinical Data Management and Clinical Safety functions to maintain data integrity and timely safety reporting. Identify and resolve operational challenges proactively to ensure project success.Strategic Support & CollaborationAssist in developing and implementing clinical trial strategies aligned with business priorities.Act as a key liaison between Clinical Operations and departments such as Regulatory Affairs, Quality, R&D, PACE, R&D, and Medical Affairs to ensure alignment and smooth communication. Manage vendor relationships and CRO oversight to meet quality standards and timelines.People Management & Team DevelopmentSupervise, mentor, and develop Clinical Operations staff to build a high-performing and engaged team. Drive performance management, goal setting, and professional growth initiatives within the team. Foster a culture of collaboration, accountability, and continuous improvement.Project ManagementDevelop and monitor project plans, resource allocation, and budgets for clinical trials. Provide regular status updates to senior leadership and escalate risks appropriately. Facilitate effective cross-functional team meetings and communication.Compliance & Quality AssuranceEnsure compliance with applicable regulatory requirements, company policies, and SOPs2. Prepare for and support audits and inspections; lead corrective and preventive actions as needed. Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization. Perform additional duties as assigned.Salary Range:
$158,000 - $195,000 Financial compensation packages may be higher/lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demands,
Confirm your E-mail: Send Email
All Jobs from MICROVENTION, INC.