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Memorial Sloan-Kettering Cancer Center Clinical Research Associate- Solid Tumor Breast 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. We’re treating cancer, one patient at a time.Join us and make a difference every day.

Job Description

Do you have at least2 years working in clinical research and have clincal trial experience?We have an exciting opportunity in our Solid Tumor Breast Service as a Clinical Research Associate (CRA).As an integral member of the research team, and in compliance with all regulatory, institutional, and departmental requirements, the CRA coordinates and maintains the assigned research portfolio for a Service and/or Department.

Are you seeking an opportunity to be at the forefront of innovation during this exciting time at Memorial Sloan Kettering Cancer Center? Our mission is the dynamic control and cure of cancer through programs of patient care, research, and education. Do you want to join a diverse team and learn how to apply your skills to support our mission? We want you to join us!

You Will:

  • Serve as the main point of contact for all research portfolio activities, and maintain real-time knowledge of every aspect of all research protocols

  • Be the critical facilitator for a multidisciplinary team encompassing data and patient management, as well as regulatory oversight

  • Effectively communicate the overall study progress to various internal and/or external partners, and identify study trends, and build/implement solutions

  • Perform diverse research-related functions using good judgment and outstanding organizational skills

    You are:

  • Adept at anticipating and prioritizing work to meet the commitments of multiple partners

  • Adept at building partnerships and working to influence others to meet shared objectives and goals

  • Known as someone who improves processes and proactively, independently identifies solutions that anticipate stakeholder needs

    You have:

  • HS Diploma/GED with 2-4 years of experience, OR Bachelor’s Degree with at least 1 full year of experience. Relevant work experience includes being part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory

  • Good Clinical Practice (GCP) and Human Subjects Protection (HSP) Certifications required

  • Proficiency with the Electronic Medical Record (EMR) system

  • Excellent computer skills, including proficiency in Microsoft Office Products and other software programs for database management/queries, generating reports and developing graphics

  • Knowledge of clinical research data collection processes in accordance with GCP


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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Job LocationsUSA-NY-New York

Posted Date6 days ago(6/10/2021 1:32 PM)

Requisition ID 2021-50727

Category Research - Clinical