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Senior Biostatistician Consultant
ProPharmaSenior Biostatistician at ProPharma leading statistical analyses for clinical trials and providing expertise to cross functional teams. Ensuring quality deliverables and maintaining compliance with regulatory standards.
ATS Keywords
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Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
statistical analysisSAS programmingR programmingclinical trial designdata analysisstatistical reportingstatistical deliverablescase report formsstandard operating proceduresquality assurance
Soft Skills
cross-functional collaborationcommunicationattention to detailproblem-solvingleadership
Certifications & Qualifications
Ph.D. in BiostatisticsM.S. in Biostatistics
Industry Keywords
biostatisticsregulatory guidelinesclinical operationsdata managementoutsourcing industryclinical study protocolsstatistical expertiseindustry standardsclinical trial datastatistical analysis guidelines
About the role
Key responsibilities & impact- Lead statistical activities for clinical trials and data analyses
- Provide statistical expertise to cross functional teams, including clinical operations, data management, and regulatory affairs
- Ensure the quality and accuracy of statistical deliverables, including statistical reports, tables, listings, and graphs
- Participate in the development and review of clinical study protocols and case report forms (CRFs)
- Develop and maintain SAS programs for statistical analysis in accordance with standard operating procedures (SOPs)
- Keep up to date with regulatory guidelines and industry standards related to biostatistics
Requirements
What you’ll need- Ph.D. in Biostatistics, or M.S. in Biostatistics
- 3+ years of relevant work experience
- Outsourcing industry experience required
- Knowledge of regulatory requirements and guidelines related to statistical analysis and reporting of clinical trial data
- Ability to program in SAS and/or R
Benefits
Comp & perks- Health insurance
- 401(k) matching
- Flexible working hours
- Paid time off