We are seeking aResearch Project Associatefor ourMulticenter Office of Clinical Research.

You Will:

• 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.

You are:

• 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.

You Need:

• 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

Hours:

• 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.

#LI-Hybrid