Clinic Research Study Specialist (Montvale, NJ)

Job Posting Number: 24348

Research – Clinical
Montvale, NJ
August 1, 2018
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 Details:

We Are:

Research is integral to our mission at Memorial Sloan Kettering, and clinical trials help us discover better forms of patient care and treatment. Our extraordinary scientists and clinicians work together to drive innovation and tackle some of the greatest challenges of biomedical science.

Memorial Sloan Kettering is seeking a Research Study Specialist (RSS) – Clinic, focusing on responsibilities related to the coordination of biospecimen and genetic protocols in clinic.

A Research Study Specialist (RSS) may be assigned to the following type of projects:

  • Clinic
  • Preceptorship of research staff
  • Special projects (i.e. short-term studies, RSA training, etc)

This is an opportunity for research staff to get experience on research projects in a variety of departments and services within the clinical research community at MSK.

You Are:

  • Curious and eager to tackle a wide variety of problems across the clinical research community at MSK
  • Adaptable to the needs of other departments and services
  • A good decision-maker, with proven success at making timely decisions that keep the organization moving forward
  • Consistently achieving results, even under tough circumstances
  • Able to hold yourself and others accountable in order to achieve goals and live up to commitments
  • An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding
  • Resilient in recovering from setbacks and skilled at finding detours around obstacles
  • Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances within the various departments
  • Interested in gaining exposure to medical terminology and the various disease types treated at MSK
  • You are comfortable with or interested in working with and organizing large amounts of data

You Will:

  • Be responsible for coordinating and performing tasks in clinic
  • Provide clinic support by assisting with patient management on study
  • Consent patients to non-therapeutic biospecimen protocols
  • Support and help ensure complete regulatory compliance and data collection in clinic
  • Coordinate meetings with the PIs and provide assistance to other RSAs as needed
  • Ensure that all appropriate institutional, state, and federal regulations are followed throughout the research protocols
  • Assist with training new staff members as needed
  • Assist with short-term projects and provide cross-coverage to various research teams

You Have:

  • A Bachelor’s degree plus two year’s clinical research experience
  • Excellent problem-solving abilities to analyze situations, draw conclusions, make recommendations as needed and convey this information in a timely and proficient manner
  • The ability to multitask and use specialized knowledge and experience to handle complex work assignments, including cross-coverage throughout the institution
  • The ideal candidate would be someone who is responsible, organized, detail-oriented, likes taking initiative, and can communicate effectively with different departments and patients


  • 9am – 5pm (Monday-Friday) with flexibility depending on clinic needs

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.