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Data Scientist I, PCCTC

Key Facts

Remote From: 
Category:  Data Scientist
Full time
English

Other Skills

  • Collaboration
  • Communication
  • Problem Solving
  • Critical Thinking
  • Detail Oriented
  • Adaptability
  • Proactivity
  • Growth Mindedness

Roles & Responsibilities

  • An undergraduate degree, preferably in statistics, data science, computer science, or a related field
  • A strong working knowledge of R for data wrangling, analysis, and visualization, and preferably have experience using packages from the Tidyverse ecosystem
  • Exposure to version control (git/GitHub)
  • Knowledge of R Markdown or Quarto

Requirements:

  • Maintain data pipelines for automated data processing suitable for downstream reporting, tabling, and summarizing
  • Execute and build upon reproducible reports via efficient code for complex tabling and data visualization
  • Contribute to internal or external R packages
  • Collaborate with Clinical Operations and Data Management teams to understand emerging trial and business needs

Job description

About Us:

   

The people of Memorial Sloan Kettering Cancer Center (MSK) are united by a singular mission: ending cancer for life. Our specialized care teams provide personalized, compassionate, expert care to patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. MSK is dedicated to training the next generation of scientists and clinicians, who go on to pursue our mission at MSK and around the globe.

 

Exciting opportunity at MSK: Join the Prostate Cancer Clinical Trials Consortium as a Data Scientist I! The Prostate Cancer Clinical Trials Consortium (PCCTC), incubated within Memorial Sloan Kettering (MSK), is seeking a Data Scientist I to join a collaborative team of clinical investigators and PCCTC staff working together on a single mission: to design, implement, and complete clinical trials and observational studies in prostate cancer, translating scientific discoveries to improve standards of care. We support this work through biostatistics and data science, data management, reporting, site management, and clinical operations across the clinical study lifecycle.

You will develop and support data workflows, reproducible reporting, and R programming solutions for clinical trial and study needs. You will work with our Data Science Team and collaborate across Clinical Operations and Data Management to deliver clear, reliable data outputs. 

Role Overview:

  • Maintain data pipelines for automated data processing suitable for downstream reporting, tabling, and summarizing  This role does not involve advanced statistical modeling or machine learning.
  • Execute and build upon reproducible reports via efficient code for complex tabling and  data visualization.
  • Contribute to internal or external R packages.
  • Collaborate with Clinical Operations and Data Management teams to understand emerging trial and business needs, assess available data, and determine how to appropriately summarize and present results.

Additionally, we wanted to share a few other tools and concepts that we work with as a team. We are excited to collaborate with you on these areas and also support your continuous development!

  • CDISC, SDTM, and ADaM
  • regulatory requirements & clinical trial design
  • complex & relational data sets
  • building Shiny applications + R packages

Key Qualifications:

  • An undergraduate degree, preferably in statistics, data science,  computer science, or a related field.
  • A strong working knowledge of R for data wrangling, analysis, and visualization, and preferably have experience using packages from the Tidyverse ecosystem.
  • Exposure to version control (git/GitHub).
  • Knowledge of R Markdown or Quarto.
  • Passion for data and creating new solutions to empower cancer care and clinical research.

Core Skills:

  • Strong collaboration skills with the ability to partner effectively across cross-functional teams
  • Excellent communication skills, with the ability to translate complex data into clear, actionable insights
  • Strong problem-solving and critical thinking abilities in a data-driven environment
  • High attention to detail with a commitment to accuracy and data quality
  • Adaptable and proactive, with a growth mindset and interest in continuous learning

Additional Information:

  • Location: Remote
  • Schedule: Monday to Friday 9 am to 5 pm EST
  • Reporting to the Senior Data Scientist

Helpful Links:

Learn more about PCCTC: The Prostate Cancer Clinical Trials Consortium (PCCTC) was initiated in 2005 by the Prostate Cancer Foundation (PCF) and the U.S. Department of Defense (DOD) Prostate Cancer Research Program (PCRP) in response to critically unmet needs in prostate cancer clinical research identified by physician investigators and patient advocates. To fulfill our mission, we developed a unique infrastructure which has fostered a culture of transparent project co-development between investigators, research sites and industry partners. Established as an independent entity in 2014, the PCCTC, LLC is now the nation’s premier multicenter clinical research organization specializing in cutting-edge prostate cancer research.

 

Pay Range: $113,100.00 - $180,900.00

 

FSLA Status: Exempt

 

Closing:

At MSK, we believe in fair, competitive pay that reflects your job, experience, and skills.

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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