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Posted Job Title
Clinical Project Manager A
Job Profile Title
Clinical Research Project Manager A
Job Description Summary
The Palliative and Advanced Illness Research (PAIR) Center is seeking two project managers to support its portfolio. The mission of the PAIR Center is to generate high-quality evidence to advance healthcare policies and practices that improve the lives of all people affected by serious illness and remove the barriers to health equity that seriously ill patients commonly face.
The first project manager will support a trial that seeks to evaluate the comparative effectiveness of generalist and specialist palliative care on patient-centered outcomes and equity of palliative care delivery among seriously ill patients admitted to two large U.S. health systems. The second will support the continued growth and operational demands of Dr. Katie Auriemma’s portfolio.
The project managers will work closely with the Principal Investigator(s) and external research partners to effectively operationalize research protocols. Specifically, the project managers will: monitor study enrollment and protocol adherence; supervise research staff; communicate with data managers and analysts regarding data processing and acquisition efforts; facilitate analysis and reporting on study metrics (data safety, compliance, benchmarks for enrollment, and finances); and contribute to proposal and manuscript writing. The project managers will be responsible for ensuring all study protocols are carried out consistently and appropriately across all clinical sites and ensuring that the projects remain within scope, budget, and timeline.
Job Description
Job Responsibilities
Manage implementation of study protocols in conjunction with investigators and clinical site partners·
Oversee the daily operations of the clinical trials, including study enrollment, intervention adherence, timely completion of project milestones, and supervision of research staff·
Liaise with data managers and analysts to streamline development of study databases, EHR-based interventions and reports, data acquisition protocols, statistical analysis plans, and reporting for study monitoring (data safety, subject accrual, outcomes assessment, adherence to protocols)·
Interface with clinical sites to ensure consistency and quality in study implementation·
Manage regulatory compliance for clinical research, including IRB submissions and progress report to trial sponsors·
Coordinate team and stakeholder meetings, document decision-making, develop manual of procedures·
Contribute to proposal development, study…