We are seeking a Research Project Associate for our Multicenter Office of Clinical Research.
Serve as the MSK point of contact for external sites in activities related to the clinical trial and maintain real-time knowledge of all aspects of the trial, including data management, subject management and regulatory oversight.
Perform diverse administrative and research-related duties requiring analysis, good judgment, comprehensive understanding of all federal regulatory standards and ICH (International Center for Harmonization) mentorship on Good Clinical Practice (GCP) and MSK CRA SOPs.
Ensure that participants are treated in accordance with the protocols and that study conduct is in accordance with the CR protocol and applicable policies and regulations.
Conduct real-time eligibility verification and risk-based monitoring (RBM) of external participants enrolled in MSK clinical trials.
Be responsible for coordination of clinical trials and the eligibility verification program
Conduct monitoring of MSK MCT IITs as directed by Multicenter Manager; Monitoring assignments will include but not be limited to: protocol compliance, data verification, and GCP/ICH requirements, in real-time
Participates in internal/external clinical trial meetings to update the study team/external sites with relevant information related to the clinical trial.
Participate in special projects and task forces as determined by management.
Capable of anticipating and stabilizing the needs of multiple partners.
Inventive, securing and deploying resources effectively and efficiently.
Adept at building partnerships and working reciprocally with others to meet shared objectives and goals.
Able to operate effectively, even when things are not clear or the way forward is not obvious.
Detail-oriented, strong written and verbal communication, ability to multitask, and excellent time management skills strongly preferred.
A self-starter/be able to turn operationalized ideas and suggestions from research team.
Must be able to work independently as well as collaborate with others.
Minimum of 2 years of relevant research experience (1 year if you have a Masters degree)
Masters degree (e.g., public health, implementation science or related field) preferred
Excellent knowledge of Microsoft Office, Excel, Access, and SPSS (or SAS, SQL)
Experience withMedidata and REDCappreferred but not required
Knowledge of Visio and/or Gant project management software is helpful
Excellent data management, organizational, oral and written communication, project coordination and interpersonal skills.
Outstanding judgment, initiative, and attention to detail
Monday - Friday, 9 AM - 5 PM
Internal Number: 2021-50532
About Memorial Sloan-Kettering Cancer Center
As one of the world's premier cancer centers, Memorial Sloan-Kettering Cancer Center is committed to exceptional patient care, leading-edge research, and 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.