Regulatory Research Project Coordinator - Sarcoma Service, Department of Medicine
Memorial Sloan-Kettering Cancer Center
July 20, 2017
New York, New York
Full-time - Experienced
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 27th 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 2016, as well as Glassdoor's annual Employees' Choice Awards 2017. We're treating cancer, one patient at a time. Join us and make a difference every day.
The Sarcoma Service within the Department of Medicine is hiring for a Regulatory Research Project Coordinator (RPC) . As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements the Research Project Coordinator performs data collection, quality control and data analysis for research projects, databases, and research protocols within Memorial Sloan Kettering Cancer Center. Responsible for data/project management activities and for data accuracy and integrity associated with clinical research within the disease management team and/or service specific level. Participates in special projects and task forces as determined by management.
Performs regular audits to ensure that the data collected is complete and accurate and to ensure that the research project was carried out as outlined.
Will be working closely with management to assist in protocols in development.
Will assist in protocol submission, drafting of consents, reviewing protocol logistics.
Assist in protocol audits- reviewing and collecting regulatory documents, provide data entry assistance if needed.
House all CVs, medical licenses, certifications and ensure they are current.
Participates in special projects and task forces as determined by management.
Utilizes appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol.
Generates reports to all necessary parties on the progress of the research project, database, or protocol, as needed.
Assists in managing departmental data. Communicates with staff at all levels (principal investigators, clinical and research support staff).
Ensures that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Ensures that research protocols are approved by the Institutional Review Board and followed as written.
Ensures that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and creates processes to ensure that goals are met.
Participates or coordinates on both interdepartmental and intradepartmental organization-wide research projects as requested.
Provides leadership, organizational, creative, or clerical support to established and new research initiatives.
At least 3 years of relevant (clinical research) experience (2 year with Masters), or as determined by hiring manager.
A minimum of a High School Diploma with at least 3 - 4 years MSKCC clinical research experience.
A Master's degree is preferred.
Must be able to work independently, be flexible, and meet tight deadlines.
Experience in clinical research and/or other applicable research investigation. Relevant graduate work would be considered in lieu of minimum experience.
Microsoft applications, database knowledge a plus.
Must have a comprehensive knowledge and understanding 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).
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.
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As one of the world's premier cancer centers, Memorial Sloan-Kettering Cancer Center is committed to exceptional patient care, leading-edge research, a...nd superb educational programs. The close collaboration between our physicians and scientists is one of our unique strengths, enabling us to provide patients with the best care available today as we work to discover more effective strategies to prevent, control, and ultimately cure cancer in the future. Our education programs train future physicians and scientists, and the knowledge and experience they gain at Memorial Sloan-Kettering has an impact on cancer treatment and the biomedical research agenda around the world.