Correlative Science Associate

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 nations 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. Its 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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