Research Project Manager, Protocol Activation Core
Memorial Sloan Kettering Cancer Center
Location: New York, New York
Internal Number: 2022-57278
As an integral member of the Protocol Activation Core and in compliance with all regulatory, institutional, and departmental requirements, the Research Project Manager (RPM) manages a team of regulatory associates responsible for regulatory management of protocol activation/study start-up. This role coordinates with other Clinical Research Administration teams to ensure that the Center goals for Time to Activation are met.
Provides leadership and oversight of regulatory study start up activities across multiple assigned departments and services to meet Center activation objectives.
Manage a team of Regulatory Research Associates. This will include hiring, training, and performance management of staff.
Work closely with the Operations and Compliance departments to ensure all activation-specific aspects of regulatory oversight are carried out for trials in the Protocol Activation Core.
Identify and maintain resources for departmental and service standards to aid in startup tool development.
Perform regular quality assurance reviews of study start-up tools for accuracy and compliance.
Able to solve problems by using a logical, systematic, sequential approach.
A successful communicator; excellent interpersonal, verbal and written communication skills.
Able to manage clinical research projects with strict deadlines.
A good decision-maker, with proven success at making timely decisions that keep the organization moving forward.
Able to hold yourself and others accountable in order to achieve goals and live up to commitments.
Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances.
Knowledgeable of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA).
A minimum of a High School Diploma with experience in clinical research or applicable experience.
Bachelors degree is preferred.
At least 3 years of experience working in clinical research, preferably with experience in the regulatory space, is required.
Monday to Friday, 9 am to 5 pm. This position will be remote, with the exception of needing to come in as needed.
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.