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Memorial Sloan-Kettering Cancer Center Research Project Associate - Multicenter Clinical Trials in New York, New York

Company Overview

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.

Job Description

Are you interested in joining a growing clinical research team? Do you want to gain experience in a dynamic setting?

We are seeking aResearch Project Associatefor ourMulticenter Clinical Trials office.

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 thatstudy 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:

  • A High School Diploma/GED with 2-4 years of clinical research experience or equivalent required.

  • Bachelor’s degree preferred with experience in clinical research and/or other applicable research investigation. Relevant graduate work considered in lieu of minimum experience.

  • Comprehensive knowledge and understanding of the regulations pertaining to human subject protection, Good Clinical Practice and other clinical research essential.


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.

Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.

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Requisition ID2019-33654

CategoryResearch - Clinical

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