Principal Statistical Programmer

This role involves providing statistical programming expertise to support clinical trials and research projects. The Principal Statistical Programmer will be responsible for developing and validating statistical programs, ensuring data integrity, and collaborating with cross-functional teams to deliver high-quality results.

Key Responsibilities:

Develop and validate statistical programs using SAS or other relevant programming languages.
Ensure data quality and integrity throughout the clinical trial lifecycle.
Collaborate with statisticians, data managers, and other stakeholders to define programming requirements.
Contribute to the development and maintenance of standard operating procedures (SOPs) and programming guidelines.
Troubleshoot and resolve programming issues in a timely manner.
Participate in the review of clinical study data and reports.

Requirements/Qualifications:

Bachelor's or Master's degree in Computer Science, Statistics, or a related field.
7 to 8 years of experience in statistical programming within the pharmaceutical or healthcare industry.
Strong proficiency in SAS programming.
Experience with clinical trial data management and analysis.
Excellent communication and collaboration skills.
Knowledge of regulatory guidelines (e.g., FDA, EMA).

About the Company: Merck Group is a global leader in the healthcare industry, dedicated to discovering, developing, and delivering innovative medicines and solutions to improve human health. The company focuses on areas of unmet medical need, striving to make a positive impact on patients' lives worldwide.