• Job Type: Officer of Administration
• Bargaining Unit:
• Regular/Temporary: Regular
• End Date if Temporary:
• Hours Per Week: 35
• Standard Work Schedule:
• Building:
• Salary Range: $69,300 - $85,000
The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting.
Position Summary
The Clinical Research Project Manager in the Department of Anesthesiology, Divisions of Critical Care Medicine and Cardiac Anesthesiology, will be responsible for managing the clinical trial projects in the lab. The lab conducts a variety of clinical research studies, including studies of sepsis, cognitive dysfunction, delirium, mechanical ventilation, and complications after surgery. This position generally reports to the Division Chief(s) of Critical Care Medicine and Cardiac Anesthesiology.
Responsibilities
• Provide leadership in developing and implementing clinical trial projects. Work closely with senior administrators to facilitate the team's work and coordinate or manage the team's initiatives and projects.
• Supervise research coordinators to ensure good clinical practice in research.
• Manage multiple large and smaller complex clinical trial projects simultaneously.
• Partner with sponsors and team leaders to strategize team project plans. Focus on critical success factors, project milestones, and deliverables and develop contingency plans.
• Lead project team meetings, including reviewing action plans and tracking project milestones. Update action plans weekly and prompt accountable individuals to ensure timely task completion. Support activities of project teams and maintain accurate documentation of team minutes.
• Design communication strategies for project progress. Ensure timely and consistent communication of project priorities, status, timelines, and deliverables to the user community.
• Design data collection methods and data analyses to support team efforts. Interpret and report data to various audiences and use data to make recommendations for process improvements.
• Ensure appropriate project prioritization and requests for resources. Ensure projects are managed and delivered on time, within budget, and meet the strategic and operational needs of the department.
• Understand the requirements of various ethical and regulatory bodies, guiding the study in conforming to those requirements, and coordinating any necessary audit processes.
• Prepare study materials and establish procedures to ensure adherence to study protocols and administrative requirements.
• Lead the recruitment, training, appraisal, retention, and supervision of study team members.
• Coordinate applications, and subsequent amendments, to ethical and regulatory bodies.
• Perform site visits to facilitate study setup and initiation, regular monitoring visits during patient recruitment, and close-out visits on study completion.
• Lead study oversight groups by organizing and facilitating meetings, providing reports and documentation to committees, and following up on agreed actions.
• Ensure timely recruitment of study participants with secure randomization processes and subsequent efficient and effective data management.
• Ensure that all study adverse events are appropriately investigated by the study staff and accurately reported to the investigators and regulatory bodies as required.
• Monitor study progress to ensure compliance with and adherence to the study plan, and identify, evaluate, and rectify problems.
• Support investigators in the collection and monitoring of study data and liaise with collaborators, study doctors, and the data manager to ensure follow-up information is kept up-to-date, accurately completed, and that loss of patient data is kept to a minimum.
• Prepare research progress and monitoring reports, organize and minute regular meetings with the appropriate Steering Committee and Data Monitoring Committees, ensuring compliance with Research Governance, Good Clinical Practice, Data Protection, and ethical requirements, as applicable.
• Provide regular and ad-hoc information, both written and verbal, to all study participants and sponsors, including reports, updates, guidance, preformed commitments, and possibly a newsletter, or similar, as appropriate.
• Coordinate the preparation and publication of data, reports, and information, ensuring compliance with applicable contractual and ethical requirements.
• Ensure the inclusion of patients and public involvement and engagement group representatives at the appropriate levels and times.
• Act as the first point of contact for all external and internal agencies.
Minimum Qualifications
• Bachelor's degree or equivalent in education and experience, plus four years of related
Location: New York, NY
Posted: Sept. 18, 2024, 9:58 a.m.
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