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Statistician - Real World Evidence

Job Summary:

We are looking for a highly motivated Statistician with a strong background in statistical analysis and real-world data analysis to contribute to our efforts in gathering and interpreting real-world evidence (RWE) for our orthopaedic medical devices. This person will be responsible for performing statistical analysis, generating insights, and collaborating with cross-functional teams to design and implement studies in support of business needs.

Essential Duties & Responsibilities:

• Provide timely and scientifically sound statistical expertise to clinical development projects.
• Provide statistical input to regulatory requests to support and contributing to clinical evidence reports.
• Collaborate with cross-functional teams to define research objectives, outcomes, and data collection methods for real-world studies.
• Develop study protocols, including sample size calculations and statistical analysis plans.
• Identify and acquire relevant real-world data sources, including electronic health records, claims databases, and patient registries.
• Ensure data quality and integrity, including data cleaning, validation, and transformation as necessary.
• Conduct advanced statistical analyses to evaluate the safety, efficacy, and performance of our orthopaedic medical devices in real-world settings.
• Apply appropriate statistical techniques, including survival analysis, propensity score matching, multivariate analysis, classification, prediction, and other modern statistical methods.
• Ensure compliance with regulatory guidelines and ethical standards for real-world evidence generation.
• Collaborate with clinical scientists, business leaders, and strategical partners, both internally and externally, to prepare and publish research results in peer-reviewed journals.
  
  

Education and Special Training Required:

• Minimum of 4 years of professional experience
• 3+ years of experience in the application of statistics to clinical trials with a Doctorate degree; or 5+ years of experience in the application of statistics to clinical trials with a Master’s degree; preferred degree in Statistics, Biostatistics, Epidemiology, data science, or a related field.
• SAS and R is preferred
  
  

Qualifications and Work Experience Required:

• Knowledge of regulatory requirements related to real-world evidence
• Experience with real-world data sources and statistical analysis of healthcare data is required. Familiarity with machine learning techniques and big data analysis is a plus.
• Knowledge of regulatory requirements related to real-world evidence.
• Excellent communication skills, both written and verbal.
• Strong problem-solving and critical-thinking abilities.
• Ability to work collaboratively in a cross-functional team environment.
• Ability to be productive and handle multiple tasks to meet deadlines in a dynamic and fast paced environment.
  
  

About Stryker

Stryker is one of the world’s leading medical technology companies and, together with our customers, is driven to make healthcare better.

The company offers innovative products and services in Medical and Surgical, Neurotechnology, Orthopedics, and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 100 million patients annually.

More information is available at stryker.com

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