Research Project Associate - Prostate Cancer Clinical Trials Consortium (PCCTC)
LocationNew York, NY
DeptResearch - Clinical
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The Prostate Cancer Clinical Trials Consortium (PCCTC) is hiring a Research Project Associate (RPA). In this role, you will be responsible for providing support to the Clinical Operations team for multi-center clinical trial activities from concept to close-out.
- Manage complex multi-institutional clinical trials across a diverse research portfolio.
- Assist in designing clinical trials including concept development, correlative and translational design, protocol and informed consent drafting, safety and regulatory document drafting, etc.
- Communicate effectively and establish strong working relationships with a diverse matrix of clinical trial sites, investigators, pharmaceutical & biotechnology partners, 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 - Clinical Operations, Informatics, Business Management, Budgets & Contracts, Editorial, etc.
- Adept at planning and prioritizing work to meet commitments aligned with organizational goals.
- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.
- Comfortable working in a fast-paced environment.
- Adept at building partnerships and working collaboratively with others to meet shared objectives and goals.
- A Bachelor's degree (preferred) with least 1 year of clinical research experience.
- Proven ability to manage clinical research projects with strict deadlines.
- Working knowledge of the Code of Federal Regulations, Good Clinical Practice, and Human Subjects Protection.
- Knowledge of clinical trial regulatory and safety management preferred.
- Strong computing skills including proficiency in MS Office products.
- Ability to solve problems by using a logical, systematic, sequential approach.
- Experience working with prostate cancer clinical trials is a plus.
- Experience working with high volume Phase 3 studies is a plus.
The Prostate Cancer Clinical Trials Consortium (PCCTC) was initiated in 2005 by the Prostate Cancer Foundation (PCF) and the U.S. Department of Defense Prostate Cancer Research Program (PCRP) in response to critically unmet needs in prostate cancer clinical research. 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. We work 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 we developed a unique infrastructure, which has fostered a culture of transparent project co-development between investigators, research sites and industry partners.
Application Hiring Process
New York, NY
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