Posted in Other about 3 hours ago.
Location: Hollywood, Florida
Location:
Hollywood, Florida
At Memorial, we are dedicated to improving the health, well-being and, most of all, quality of life for the people entrusted to our care. An unwavering commitment to our service vision is what makes the difference. It is the foundation of The Memorial Experience.
Summary:
Reporting to the Director of Clinical Research, the Clinical Research Regulatory Manager supports and oversees regulatory affairs operations. The primary responsibility will be to manage the overall regulatory process and identify issues, and to independently determine whether the components of the research studies are in compliance with federal, state and local regulations, MHS policies, IRB requirements, and accreditation standards.
Responsibilities:
Coordinate new protocol submissions, renewals, and revisions to Local and Central Institutional Review Board for multiple studies.Monitor Institutional Review Board submissions, IND/IDE and respond to requests and questions. Support internal stakeholders with regulatory/compliance examination requests and drafting responses to regulatory findings.Hire, orient, train, and conduct performance reviews for staff handling research and regulatory administration activities associated with the conducting of clinical trials. Review the work of research staff when necessary to identify regulatory and compliance issues and provide advice or training.Provide direction to a team of regulatory coordinators that submit industry and national sponsored trials to IRB and safety committees for approval according to established policies and guidance.Enhance research portfolio through communications with sponsors and academic partners and coordinate site visits.Audit operations and data submission, including clinical and laboratory procedures, to ensure compliance with applicable regulations. Draft reports for senior management and external regulatory bodies as appropriate.
Competencies:
ACCOUNTABILITY, ACCURACY, CUSTOMER SERVICE, DEVELOPS RELATIONSHIPS, EFFECTIVE COMMUNICATION, PROJECT MANAGEMENT, RESEARCH - BUDGETING, RESPONDING TO CHANGE, STANDARDS OF BEHAVIOR
Education and Certification Requirements:
Bachelors (Required)
Additional Job Information:
Complexity of Work: This role requires critical thinking skills, effective communication, decisive judgment, and the ability to build and foster positive relationships. The incumbent must be able to lead others and take appropriate action when required. Required Work Experience: Five (5) years of related clinical research regulatory experience required. Other Information: Previous managerial experience preferred.Additional Education Info: Foreign Medical Degree or 10 years of related research experience in lieu of Bachelors degree is acceptable.
Working Conditions and Physical Requirements:
UPS
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Davidson Hospitality Group
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Davidson Hospitality Group
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