Entrada Therapeutics
Statistical Programmer (PART-TIME, CONTRACT)
Entrada Therapeutics, Boston, Massachusetts, us, 02298
Statistical Programmer (PART-TIME, CONTRACT)
Join to apply for the
Statistical Programmer (PART-TIME, CONTRACT)
role at
Entrada Therapeutics . Overview
We are seeking a highly skilled and detail-oriented Statistical Programmer to join Entrada Therapeutics on a part-time contract basis. This role will support biometric initiatives by developing and validating statistical programs for data analysis, reporting and presentation. The ideal candidate will have strong experience in both SAS and R programming, and a solid understanding of clinical trial data standards and regulatory requirements. This position reports to the Senior Director, Biometrics and collaborates closely with cross-functional teams including Biostatistics, Data Management, and Clinical Operations. Responsibilities
Develop, validate, and/or maintain statistical programs using SAS or R to support clinical trial data analysis, reporting, and regulatory submissions. Generate CDISC-compliant datasets (SDTM and ADaM) and outputs including tables, listings, and figures (TLFs). Perform quality control checks of programs and outputs to ensure accuracy and compliance with internal standards and regulatory guidelines. Collaborate with biostatisticians to implement analysis plans and customize outputs for target audiences. Support programming deliverables for ongoing clinical studies, including interim analyses and final study reports. Participate in the review of statistical analysis plans (SAPs), TLF shells, and other study documentation. Contribute to process improvement initiatives and development of standard macros and programming best practices. Communicate and escalate risks or issues related to programming deliverables in a timely manner. Qualifications / The Necessities
Bachelor’s or Master’s degree in Statistics, Computer Science, or a related scientific discipline. Minimum 5 years of experience in clinical programming within the pharmaceutical, biotech, or CRO industry. Proficiency in SAS (Base, Macro, Graph) or R programming is required. Strong understanding of CDISC standards (SDTM, ADaM) and experience with electronic data capture (EDC) systems and integration of data from multiple sources. Familiarity with ICH GCP guidelines and regulatory submission requirements. Experience with rare disease therapeutic areas is a plus. Excellent problem-solving skills and attention to detail. Strong verbal and written communication skills. Ability to work independently and manage multiple priorities in a remote setting. This is a US-based remote, part-time contract position with flexible hours averaging ~10 hours per week. Occasional travel to Entrada’s Boston headquarters may be required. Equal Opportunity Employer
Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law. Other
To thrive on our team, you will need to demonstrate humanity, tenacity, creativity, collaboration, and curiosity in line with Entrada’s values. Location & Travel
Remote (US-based) with occasional travel to Boston, MA headquarters.
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Join to apply for the
Statistical Programmer (PART-TIME, CONTRACT)
role at
Entrada Therapeutics . Overview
We are seeking a highly skilled and detail-oriented Statistical Programmer to join Entrada Therapeutics on a part-time contract basis. This role will support biometric initiatives by developing and validating statistical programs for data analysis, reporting and presentation. The ideal candidate will have strong experience in both SAS and R programming, and a solid understanding of clinical trial data standards and regulatory requirements. This position reports to the Senior Director, Biometrics and collaborates closely with cross-functional teams including Biostatistics, Data Management, and Clinical Operations. Responsibilities
Develop, validate, and/or maintain statistical programs using SAS or R to support clinical trial data analysis, reporting, and regulatory submissions. Generate CDISC-compliant datasets (SDTM and ADaM) and outputs including tables, listings, and figures (TLFs). Perform quality control checks of programs and outputs to ensure accuracy and compliance with internal standards and regulatory guidelines. Collaborate with biostatisticians to implement analysis plans and customize outputs for target audiences. Support programming deliverables for ongoing clinical studies, including interim analyses and final study reports. Participate in the review of statistical analysis plans (SAPs), TLF shells, and other study documentation. Contribute to process improvement initiatives and development of standard macros and programming best practices. Communicate and escalate risks or issues related to programming deliverables in a timely manner. Qualifications / The Necessities
Bachelor’s or Master’s degree in Statistics, Computer Science, or a related scientific discipline. Minimum 5 years of experience in clinical programming within the pharmaceutical, biotech, or CRO industry. Proficiency in SAS (Base, Macro, Graph) or R programming is required. Strong understanding of CDISC standards (SDTM, ADaM) and experience with electronic data capture (EDC) systems and integration of data from multiple sources. Familiarity with ICH GCP guidelines and regulatory submission requirements. Experience with rare disease therapeutic areas is a plus. Excellent problem-solving skills and attention to detail. Strong verbal and written communication skills. Ability to work independently and manage multiple priorities in a remote setting. This is a US-based remote, part-time contract position with flexible hours averaging ~10 hours per week. Occasional travel to Entrada’s Boston headquarters may be required. Equal Opportunity Employer
Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law. Other
To thrive on our team, you will need to demonstrate humanity, tenacity, creativity, collaboration, and curiosity in line with Entrada’s values. Location & Travel
Remote (US-based) with occasional travel to Boston, MA headquarters.
#J-18808-Ljbffr