Job Board

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.

In compliance with applicable New York and New Jersey State regulatory authorities, COVID-19 vaccination (2 doses of either the Pfizer or Moderna vaccine or one dose of the Johnson & Johnson vaccine) is mandatory for all MSK employees, contingent workers, and volunteers. Exceptions are permitted for those employees who request and receive an approved medical or fully remote exemption.

*Staff working at a MSK New Jersey location must be up to date with COVID-19 vaccination, which includes having completed the primary COVID-19 vaccination series and booster once eligible as mandated by New Jersey State. All New Jersey staff not yet eligible for a booster must receive a booster within 3 weeks of becoming eligible as a condition of continued employment at MSK.

Note: Individuals are eligible to receive a COVID-19 booster five months after receiving the second dose of either the Pfizer or Moderna vaccine or two months after the J&J vaccine.

Job Description

The Prostate Cancer Clinical Trials Consortium is currently hiring an experienced Correlative Science Associate to join our dynamic clinical research team. Join us today and help make a difference every day!

The Prostate Cancer Clinical Trials Consortium (PCCTC) is the nation's premier multicenter Clinical Research Organization specializing in ground breaking prostate cancer research. We work together with distinguished investigators on a single mission: to design, implement and complete hypothesis-driven studies in prostate cancer, translating scientific discoveries to improved standards of care.

You will:

• Support complex correlative studies as part of therapeutic clinical trials, registries, and non-therapeutic correlative studies across a diverse research portfolio.
• Assist in developing clinical trial materials including correlative and translational manuals, such as lab manuals, as well as other study tools to facilitate accurate and timely correlative sample collection and related data collection.
• Communicate and build strong working relationships with a diverse matrix of clinical trial sites, investigators, laboratory partners, pharmaceutical and biotechnology partners, and other important stakeholders.
• Synthesize sophisticated correlative study information into meaningful plans and manuals.
• Provide vital documentation in compliance with existing standard operating procedures, regulatory guidelines, etc.
• Assist in maintaining necessary clinical trial conduct documentation.

You Are:

• Comfortable working in a fast-paced environment.
• Dedicated to accuracy with high attention-to-detail.
• Adept at planning and prioritizing work to complete daily and ongoing tasks within required timelines.
• An effective communicator, capable of determining how best to reach different audiences and communicating based on that understanding.

You Have:

• 2 - 7 years of relevant clinical research, laboratory and/or medical/science experience.
• Strong working knowledge of translational research and correlative science; oncology related knowledge and/or experience is a plus.
• Experience with clinical trial execution preferred.
• Working knowledge of the Code of Federal Regulations, Good Clinical Practice, and Human Subjects Protection guidelines preferred.
• Strong organizational, prioritization, and time management skills.
• Ability to solve problems using a logical, detailed, sequential approach.

This is a full-time remote position.

We believe in communication, openness, and thinking beyond your 8-hour day @ MSK. It's important to us that you have a sense of impact, community, and work/life balance. We want you to be and feel your best!

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Closing

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.