Manager, Biostatistics

EPM Scientific; King of Prussia (PA); On-site; USD 140,000 - 180,000; Full time

Job summary

EPM Scientific in King of Prussia, PA is seeking a Manager, Biostatistics to lead statistical activities across clinical development and post-marketing research. You will design studies, analyze data, and provide statistical insights to support key development decisions.

PhD or relevant Master's with pharma/biotech experience required; strong R and/or SAS programming skills and familiarity with regulatory guidelines are essential.

Qualifications

• PhD or similar in biostatistics or quantitative field.
• Experience with design, analysis and interpretation of clinical trials.
• Knowledge of regulatory guidance and drug development standards.

Responsibilities

• Perform statistical analyses to support clinical development and research objectives.
• Collaborate with statisticians, programmers, and cross-functional teams for timely deliverables.
• Contribute to study design, SAPs, and statistical methodology.
• Analyze data from trials and real-world sources to support evidence generation.
• Partner with Clinical Development, Medical Affairs, and CROs.
• Support innovative statistical approaches and contribute to publications and conferences.

Skills

R

SAS

Clinical trials

Regulatory knowledge

Education

PhD in Biostatistics or related quantitative discipline

Master's degree with pharma/biotech experience

Job description

Manager, Biostatistics (PR/615195) King of Prussia, Pennsylvania

Salary: USD140000 - USD180000 per year

Location: King of Prussia, PA (3 days a week onsite)

Aleading biopharmaceutical organization is seeking a Manager, Biostatistics to support statistical activities across clinical development and post-marketing research programs. ThisBiostatistics leader will work closely with cross-functional teams to design studies, analyze clinical data, and provide statistical insights that support key development decisions.

Key Responsibilities

• Perform statistical analyses to support clinical development and research objectives.
• Collaborate with biostatisticians, statistical programmers, and cross-functional stakeholders to ensure timely and high-quality deliverables.
• Contribute to clinical study design, protocol development, and the creation of Statistical Analysis Plans (SAPs).
• Analyze data from clinical trials, observational studies, and real-world data sources to support evidence generation initiatives.
• Partner closely with Clinical Development, Medical Affairs, Clinical Operations, Data Management, and external vendors/CROs.
• Support innovative statistical approaches and contribute to scientific publications, presentations, and external conferences.

Qualifications

• PhD in Biostatistics, Statistics, or a related quantitative discipline; Master's degree candidates with relevant pharmaceutical or biotechnology industry experience will also be considered.
• Experience supporting the design, analysis, and interpretation of clinical trials and healthcare-related datasets.
• Strong statistical programming skills using R and/or SAS.
• Understanding of clinical development processes and statistical methodologies used in drug development.
• Familiarity with regulatory guidance and industry standards.