Sr. Lead Biostatistician - Oncology Evidence Generation

Minimum Requirements:

• MS in Biostatistics, Statistics, or a related quantitative field 
• 6 or more years of experience in clinical biostatistics within biotechnology, diagnostics, CRO, or related healthcare environments 
• 5 or more years of experience in statistical programming (R, SAS or equivalent acceptable) 
• 3 or more years of experience supporting clinical research studies, including observational studies, registries, and/or assay validation efforts 
• 3 or more years of experience independently managing statistical analyses and deliverables across multiple concurrent studies 

Preferred Requirements:

• PhD in Biostatistics, Statistics, or a related quantitative field 
• 3 or more years of experience in oncology research, biomarker-driven studies, or precision oncology 
• 3 or more years of experience with real-world data, registry-based research, or observational study designs 
• 3 or more years of experience contributing to scientific publications, including abstracts, manuscripts, or conference presentations 
• 1 or more years of experience with MRD, ctDNA, genomics/NGS-based assays, or molecular diagnostics 
• 1 or more years of experience with clinical study documentation and regulatory standards (e.g., protocols, SAPs, GCP principles) 

Additional Job Standards:

• Strong foundation in clinical study design and applied statistical leadership, including sample size estimation, power calculations, and endpoint evaluation 
• Experience applying statistical methods to clinical, real-world, and/or assay validation datasets, including regression and survival/time-to-event analysis 
• Strong written and verbal communication skills, with ability to clearly convey complex statistical concepts to diverse scientific and non-technical audiences 
• Demonstrated ability to work effectively in cross-functional teams and collaborate with internal stakeholders and external partners 
• Strong analytical, problem-solving, and organizational skills, with high attention to detail and commitment to data quality and scientific rigor 
• Experience working in collaborative research environments involving academic or external investigator partnerships 
• Occasional travel for internal meetings or external collaborator engagement, as needed (≤10–15%) 

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. For more detailed information, please click here. 

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

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