Associate Director, Biostatistics
Firma Clinical Research, LLC, Elk Grove Village, Illinois, us, 60009
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Full Time Management Elk Grove Village, IL, US
6 days ago Requisition ID: 1023
Location:
Remote – United States Company:
Firma Clinical Research Employment Type:
Full-Time About Firma Clinical Research Firma Clinical Research is a growing clinical research organization committed to delivering high-quality, data-driven solutions to our biopharmaceutical and healthcare partners. We pride ourselves on scientific rigor, collaboration, and a people-first culture that values innovation, integrity, and excellence. Position Overview Firma Clinical Research is seeking an experienced
Associate Director, Biostatistics
to join our team in a fully remote capacity. This role serves as a first-line people manager and scientific leader, with accountability for statistical quality, project delivery, and team development across multiple clinical studies. The ideal candidate brings a strong blend of
technical biostatistics expertise, leadership capability, and exceptional communication skills , with the ability to collaborate cross-functionally in a remote environment. Key Responsibilities Lead and manage a team of statisticians, ensuring high-quality deliverables and adherence to study timelines Assign and oversee statistical resources across multiple clinical projects Provide scientific and strategic input to clinical development programs Prepare, review, and approve clinical study protocols, Statistical Analysis Plans (SAPs), table shells, and related documentation Collaborate closely with Programming, Data Management, Clinical Operations, and other cross-functional teams Review and contribute to clinical study reports, regulatory submissions, and study result presentations Mentor, coach, and develop junior statisticians, fostering professional growth and technical excellence Apply regulatory guidance and advanced statistical methodologies to support drug development Identify and implement innovative statistical approaches that add value to client programs Qualifications Master’s degree in Biostatistics, Statistics, Mathematics, or a related field (PhD preferred) Minimum
7 years of clinical trials experience
with a Master’s degree, or
5 years with a PhD Strong working knowledge of
SAS and/or R ; experience with additional statistical software is a plus Demonstrated leadership experience managing projects and/or teams Solid understanding of statistical models used in pharmaceutical development and healthcare research Excellent
verbal, written, and presentation skills , with the ability to communicate complex concepts clearly to diverse audiences Proven ability to work effectively in a
remote, collaborative environment Why Join Firma? Fully remote role with flexibility Opportunity to lead impactful clinical research programs Collaborative, growth-oriented culture Competitive compensation and benefits Meaningful leadership and career advancement opportunities Equal Opportunity Employer Firma Clinical Research is an equal opportunity employer and values diversity in the workplace. We are committed to creating an inclusive environment for all employees.
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Remote – United States Company:
Firma Clinical Research Employment Type:
Full-Time About Firma Clinical Research Firma Clinical Research is a growing clinical research organization committed to delivering high-quality, data-driven solutions to our biopharmaceutical and healthcare partners. We pride ourselves on scientific rigor, collaboration, and a people-first culture that values innovation, integrity, and excellence. Position Overview Firma Clinical Research is seeking an experienced
Associate Director, Biostatistics
to join our team in a fully remote capacity. This role serves as a first-line people manager and scientific leader, with accountability for statistical quality, project delivery, and team development across multiple clinical studies. The ideal candidate brings a strong blend of
technical biostatistics expertise, leadership capability, and exceptional communication skills , with the ability to collaborate cross-functionally in a remote environment. Key Responsibilities Lead and manage a team of statisticians, ensuring high-quality deliverables and adherence to study timelines Assign and oversee statistical resources across multiple clinical projects Provide scientific and strategic input to clinical development programs Prepare, review, and approve clinical study protocols, Statistical Analysis Plans (SAPs), table shells, and related documentation Collaborate closely with Programming, Data Management, Clinical Operations, and other cross-functional teams Review and contribute to clinical study reports, regulatory submissions, and study result presentations Mentor, coach, and develop junior statisticians, fostering professional growth and technical excellence Apply regulatory guidance and advanced statistical methodologies to support drug development Identify and implement innovative statistical approaches that add value to client programs Qualifications Master’s degree in Biostatistics, Statistics, Mathematics, or a related field (PhD preferred) Minimum
7 years of clinical trials experience
with a Master’s degree, or
5 years with a PhD Strong working knowledge of
SAS and/or R ; experience with additional statistical software is a plus Demonstrated leadership experience managing projects and/or teams Solid understanding of statistical models used in pharmaceutical development and healthcare research Excellent
verbal, written, and presentation skills , with the ability to communicate complex concepts clearly to diverse audiences Proven ability to work effectively in a
remote, collaborative environment Why Join Firma? Fully remote role with flexibility Opportunity to lead impactful clinical research programs Collaborative, growth-oriented culture Competitive compensation and benefits Meaningful leadership and career advancement opportunities Equal Opportunity Employer Firma Clinical Research is an equal opportunity employer and values diversity in the workplace. We are committed to creating an inclusive environment for all employees.
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