Employment Type: Full-Time
Industry: Non-Executive Management
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Company Overview At Memorial Sloan Kettering (MSK), we're not only changing the way we treat cancer, but also the way the world thinks about it. By working together and pushing forward with innovation and discovery, we're driving excellence and improving outcomes. For the 28th year, MSK has been named a top hospital for cancer by U.S. News & World Report. We are proud to be on Becker's Healthcare list as one of the 150 Great Places to Work in Healthcare in 2018, as well as one of Glassdoor's Employees' Choice Best Place to Work for 2018. We're treating cancer, one patient at a time.Join us and make a difference every day. Job Description The Prostate Cancer Clinical Trials Consortium (PCCTC) is hiring a Research Program Manager. As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the Research Program Manager collaborates directly with the Director of Research Operations to provide leadership in developing and improving the conduct of multi-center clinical trial activities. Commitment to accuracy, high attention-to-detail, and ability to work independently are critical competencies for the role. More information about the PCCTC: The Prostate Cancer Clinical Trials Consortium (PCCTC) was initiated in 2005 by the Prostate Cancer Foundation (PCF) and the U.S. Department of Defense (DOD) Prostate Cancer Research Program (PCRP) in response to critically unmet needs in prostate cancer clinical research identified by physician investigators and patient advocates. Established as an independent entity in 2014, the PCCTC, LLC is now the nation's premier multicenter Clinical Research Organization (CRO) specializing in cutting-edge prostate cancer research. The PCCTC works together with distinguished investigators on a single mission: to design, implement and complete hypothesis-driven early phase trials in prostate cancer, translating scientific discoveries to improved standards of care. To fulfill its mission, the PCCTC developed a unique infrastructure, which has fostered a culture of transparent project co-development between investigators, research sites and industry partners. You will: + Directs staff functions, activities, and priorities to ensure workflow supports PCCTC business needs. Communicates and ensures compliance with PCCTC policies and procedures, quality standards and improvement initiatives. + Plays a leadership role in the development and management of clinical research throughout the business. This program includes but is not limited to: CR portfolio management and oversight, protocol development including budgets, contracts, tools and appropriate protocol documents, protocol review process, on-going study activities and quality. + Develop long and short-term goals, anticipate the effects of changing regulatory requirements, and support PCCTC standards to support the conduct of multi-institutional clinical trials. + Implements solutions for streamlining and accelerating the monitoring and review of clinical trials data to significantly increase accrual to clinical trials, data cleaning, data quality, and trial completion. + Forecast trial resource needs and assess staffing resource needs for program and ensure an adequate balance between PCCTC research mission and its fiscal responsibilities. + Communicate effectively by establishing strong working relationships with a diverse matrix of clinical trial sites, investigators, pharmaceutical & biotechnology executives, and other important stakeholders. + Synthesize complex clinical, regulatory, and other clinical trial information into actionable plans. + Provide necessary documentation in compliance with existing standard operating procedures, regulatory guidelines, etc. + Assist in maintaining necessary clinical trial conduct documentation (includes Project Management Plans, Safety Management Plans, Monitoring Plans, Meeting Minutes, etc.). + Communicate and work effectively with all stakeholders of the PCCTC - Executive Leadership, Clinical Operations, Informatics, Business Management, Budgets & Contracts, Editorial, etc. You need: + 7-10 years of technical, operational and managerial clinical research experience, or as determined by hiring manager. + A Masters degree is preferred. + Therapeutic and Oncology Research experience strongly preferred. + Proven ability to manage clinical research projects with strict deadlines. + Thorough knowledge and experience with clinical trial execution. + Thorough knowledge of the Code of Federal Regulations, Good Clinical Practice, and Human Subjects Protection. + Thorough knowledge of clinical trial regulatory and safety management. + Comfortable working in a fast-paced environment. + Strong organizational, prioritization, and project management skills. + Strong computing skills including proficiency in MS Office products. + Excellent interpersonal, verbal and written communication skills. + Ability to solve problems by using a logical, systematic, sequential approach. + Experience working with prostate cancer clinical trials and/or multicenter projects is a plus.#LI-POST Closing MSK is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sexual orientation, national origin, age, religion, creed, disability, veteran status or any other factor which cannot lawfully be used as a basis for an employment decision. Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Refer this job to a friend Stay in touch! Register now to join Memorial Sloan Kettering'sto receive inside information on our organization and new job opportunities. Requisition ID2019-37691 CategoryResearch - Other
Associated topics: chief program officer, cpo, manage, manager, management, monitor, product manager, project manager, relationship manager, task
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