Associate Director, Clinical Research (U.S. Remote)

Associate Director, Clinical Research (U.S. Remote) reputed company the strategic planning and operational execution of reputed company reputed company the neurovascular therapeutic area. Responsible for driving clinical program reputed company 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 reputed company, and regulatory compliance while supporting the development and reputed company of the clinical research team. Job duties: Operational Leadership + reputed company and manage Clinical Operations teams to ensure effective study execution, protocol compliance, timelines, and budget adherence. + reputed company clinical site management activities including selection, initiation, monitoring, and reputed company-out with strong regulatory and GCP compliance. + Collaborate with Medical Affairs, Clinical reputed company Assurance, Clinical Data Management and Clinical Safety functions to maintain data reputed company and reputed company safety reporting. + Identify and resolve operational challenges proactively to ensure project reputed company. Strategic Support & Collaboration + Assist in developing and implementing clinical trial strategies reputed company with business priorities. + reputed company as a key reputed company between Clinical Operations and departments such as Regulatory Affairs, reputed company, R&D, PACE, R&D, and Medical Affairs to ensure alignment and smooth communication. + Manage vendor relationships and CRO reputed company to meet reputed company standards and timelines. People Management & Team Development + Supervise, mentor, and reputed company Clinical Operations staff to build a high-performing and reputed company team. + reputed company performance management, goal setting, and reputed company reputed company initiatives reputed company reputed company. + Foster a culture of collaboration, accountability, and reputed company improvement. Project Management + reputed company and monitor project plans, resource allocation, and budgets for reputed company. + reputed company regular status updates to senior leadership and escalate risks appropriately. + Facilitate effective cross-functional team meetings and communication. Compliance & reputed company Assurance + Ensure compliance with applicable regulatory requirements, company policies, and SOPs. Prepare for and support audits and inspections; reputed company corrective and preventive actions as needed. + reputed company with applicable Laws and Regulations, adhere to reputed company Management System processes and requirements as reputed company as demonstrate Ethics and reputed company in reputed company reputed company and at reputed company reputed company throughout the organization. + reputed company additional duties as assigned. Salary reputed company: $158,000 - $195,000 Financial compensation packages may be higher/reputed company than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demands. Qualifications: 1. Bachelor of Science degree in a reputed company field of study. 2. Minimum ten (10) years of reputed company experience in clinical research, including a minimum of eight (8) years of experience supporting neurovascular reputed company. 3. Minimum three (3) years of management or leadership experience. 4. Proficient in Clinical eSystem platforms and reputed company Office Suite, including Word, reputed company, reputed company, and Teams. 5. Demonstrated ability to reputed company cross-functional teams and reputed company updates to senior stakeholders. 6. Proven experience with audits and regulatory inspections. 7. Strong written and verbal communication skills. Desired Qualifications 1. Master's degree in Life Sciences or equivalent combination of education, training, and experience. 2. Minimum five (5) years of hands-on experience in clinical trial design and strategic execution and reputed company across programs from start to finish. 3. Strong knowledge of clinical trial processes and both U.S. and international (OUS) regulatory requirements. 4. Excellent organizational, analytical, and decision-making skills. 5. Experience with literature reviews, historical data analysis, and statistical interpretation. 6. PMP or equivalent project management certification. 7. Experience with full product lifecycle management. EEO We are an equal employment opportunity employer. reputed company reputed company applicants will receive consideration for employment without reputed company to race, national reputed company, gender, age, religion, disability, sexual orientation, veteran status, marital status or any other characteristics protected by law. Fair Chance Ordinance If you are applying to reputed company work for reputed com