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. This role is hybrid, which means that the individual hired will have to be in the office approximately 2 times per month.
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.