Based on company needs, this position will be required to lead one or more early Phase or late ... Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response), blank and annotated CRFs ...
Based on company needs, this position will be required to lead one or more early Phase or late ... Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response), blank and annotated CRFs ...
Based on company needs, this position will be required to lead one or more early Phase or late ... Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response), blank and annotated CRFs ...
Based on company needs, this position will be required to lead one or more early Phase or late ... Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response), blank and annotated CRFs ...
Based on company needs, this position will be required to lead one or more early Phase or late ... Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response), blank and annotated CRFs ...
Based on company needs, this position will be required to lead one or more early Phase or late ... Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response), blank and annotated CRFs ...
Based on company needs, this position will be required to lead one or more early Phase or late ... Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response), blank and annotated CRFs ...
Based on company needs, this position will be required to lead one or more early Phase or late ... Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response), blank and annotated CRFs ...
... Lead statistical programming activities for multiple clinical research projects in pharmaceutical or CRO settings. - Utilize SAS (and other statistical software) to conduct statistical analyses ...
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... Lead statistical programming activities for multiple clinical research projects in pharmaceutical or CRO settings. - Utilize SAS (and other statistical software) to conduct statistical analyses ...
Based on company needs, this position may be required to lead an early Phase or late phase study or ... Ensure quality and timely delivery of analysis for statistical programming deliverables. * Provide ...
Based on company needs, this position may be required to lead an early Phase or late phase study or ... Ensure quality and timely delivery of analysis for statistical programming deliverables. * Provide ...
Based on company needs, this position may be required to lead an early Phase or late phase study or ... Ensure quality and timely delivery of analysis for statistical programming deliverables. * Provide ...
Based on company needs, this position may be required to lead an early Phase or late phase study or ... Ensure quality and timely delivery of analysis for statistical programming deliverables. * Provide ...
Plays a lead role in hiring, training, coaching, and oversight of in-house and contract statistical programmers supporting the analysis and reporting of clinical and nonclinical data for corporate ...
Plays a lead role in hiring, training, coaching, and oversight of in-house and contract statistical programmers supporting the analysis and reporting of clinical and nonclinical data for corporate ...
Plays a lead role in hiring, training, coaching, and oversight of in-house and contract statistical programmers supporting the analysis and reporting of clinical and nonclinical data for corporate ...
Plays a lead role in hiring, training, coaching, and oversight of in-house and contract statistical programmers supporting the analysis and reporting of clinical and nonclinical data for corporate ...
Plays a lead role in hiring, training, coaching, and oversight of in-house and contract statistical programmers supporting the analysis and reporting of clinical and nonclinical data for corporate ...
Plays a lead role in hiring, training, coaching, and oversight of in-house and contract statistical programmers supporting the analysis and reporting of clinical and nonclinical data for corporate ...
Sr. Analyst, Stats Programming
San Diego, CA ยท On-site
... statistical programming efforts for clinical and non-clinical projects and studies. Provides ... In addition, must have at least three years of experience serving in a supervisory or lead capacity.
Sr. Analyst, Stats Programming
San Diego, CA ยท On-site
... statistical programming efforts for clinical and non-clinical projects and studies. Provides ... In addition, must have at least three years of experience serving in a supervisory or lead capacity.
Senior Principal Statistician
South San Francisco, CA ยท On-site
$104K - $128K/yr
As trusted analytical partners in end-to-end drug development, Biostatistics leverages data to ... You lead statistical design and strategy for the molecule CDP, developing innovative approaches ...
Senior Principal Statistician
South San Francisco, CA ยท On-site
$104K - $128K/yr
As trusted analytical partners in end-to-end drug development, Biostatistics leverages data to ... You lead statistical design and strategy for the molecule CDP, developing innovative approaches ...
Senior Principal Statistician
$104K - $128K/yr
As trusted analytical partners in end-to-end drug development, Biostatistics leverages data to ... You lead statistical design and strategy for the molecule CDP, developing innovative approaches ...
Senior Principal Statistician
$104K - $128K/yr
As trusted analytical partners in end-to-end drug development, Biostatistics leverages data to ... You lead statistical design and strategy for the molecule CDP, developing innovative approaches ...
Senior Statistician
South San Francisco, CA ยท On-site
$136K - $254K/yr
As trusted analytical partners in end-to-end drug development, Biostatistics leverages data to ... You independently lead statistical input into clinical trial design, aligning with scientific ...
Senior Statistician
South San Francisco, CA ยท On-site
$136K - $254K/yr
As trusted analytical partners in end-to-end drug development, Biostatistics leverages data to ... You independently lead statistical input into clinical trial design, aligning with scientific ...
Senior Statistician
South San Francisco, CA ยท On-site
$136K - $254K/yr
As trusted analytical partners in end-to-end drug development, Biostatistics leverages data to ... You independently lead statistical input into clinical trial design, aligning with scientific ...
Senior Statistician
South San Francisco, CA ยท On-site
$136K - $254K/yr
As trusted analytical partners in end-to-end drug development, Biostatistics leverages data to ... You independently lead statistical input into clinical trial design, aligning with scientific ...
Senior Statistician, Early Development
South San Francisco, CA ยท On-site
$104K - $128K/yr
You independently lead statistical input into early phase clinical trial designs, ensuring ... You design and execute complex analyses, often involving PK PD modeling, exploratory biomarker data ...
Senior Statistician, Early Development
South San Francisco, CA ยท On-site
$104K - $128K/yr
You independently lead statistical input into early phase clinical trial designs, ensuring ... You design and execute complex analyses, often involving PK PD modeling, exploratory biomarker data ...
Senior Statistician, Early Development
South San Francisco, CA ยท On-site
$104K - $128K/yr
You independently lead statistical input into early phase clinical trial designs, ensuring ... You design and execute complex analyses, often involving PK PD modeling, exploratory biomarker data ...
Senior Statistician, Early Development
South San Francisco, CA ยท On-site
$104K - $128K/yr
You independently lead statistical input into early phase clinical trial designs, ensuring ... You design and execute complex analyses, often involving PK PD modeling, exploratory biomarker data ...
Senior Manager, Biostatistics
San Carlos, CA ยท On-site
Responsible for study design, statistical analysis, interpretation of results, and communication of statistical findings. Responsibilities: * Serve as lead statistician for one or more clinical ...
Senior Manager, Biostatistics
San Carlos, CA ยท On-site
Responsible for study design, statistical analysis, interpretation of results, and communication of statistical findings. Responsibilities: * Serve as lead statistician for one or more clinical ...
Associate Director, Biometrics
Carlsbad, CA ยท On-site
Lead review and discussion of SAP. * Oversee CRO statistical activities and deliverables (quality, timelines, and SAP implementation). * Maintain study documentation of statistical analyses and ...
Associate Director, Biometrics
Carlsbad, CA ยท On-site
Lead review and discussion of SAP. * Oversee CRO statistical activities and deliverables (quality, timelines, and SAP implementation). * Maintain study documentation of statistical analyses and ...
$127K - $236K/yr
Lead technical review of statistical analysis products. Support failure investigations. Lead or direct proposal efforts. Identify and lead discipline initiatives and coordination meetings. * Expertly ...
$127K - $236K/yr
Lead technical review of statistical analysis products. Support failure investigations. Lead or direct proposal efforts. Identify and lead discipline initiatives and coordination meetings. * Expertly ...
Lead Statistical Analyst information
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Principal Statistical Analyst
Redwood City, CA โข Hybrid
Full-time
Re-posted 28 days ago
Job description
The Opportunity:
Position requires 14+ years of Statistical Programming experience with exploratory-stage oncology clinical trials, providing programming support and oversight of one or more clinical programs (early or late phase) within Statistical Programming function. In addition to hands-on Programming, this position requires providing oversight and programming support and guidance for internal deliverables and regulatory submissions while ensuring conformance to CDISC standards and submission guidelines. Based on company needs, this position will be required to lead one or more early Phase or late phase studies/programs. Specific responsibilities include:
Effective collaborating with cross functional teams to provide programming timelines for various deliverables.
Provide SAS Programming technical support and guidance to programming team.
Oversight/participation in any internal/mock or regulatory authority audits.
Timeline and vendor management for deliverables, including submission-related activities, ย complying with regulatory standards (e.g., FDA 21 CFR Part 11, GxP).
Oversee the programming support for relevant deliverables, such as Investigator Brochures, publications, US and ex-US regulatory submissions, including CDISC compliant datasets (SDTM, ADaM) and data documentation, Reviewer's Guide, TLFs, Statistical Analysis Plans (study specific, ISS, ISE, Exposure-Response), blank and annotated CRFs, and actual patient CRFs.
Hands-on programming and management of in-house deliverables including but not limited to Dose Committee meetings, Board of Director meetings, Exploratory Analysis, etc.
Oversight and Verification Review of documents, spreadsheets, slides for in-house presentations and external publications.
Titles may vary based on candidate experience.
Required Skills, Experience and Education:
14+ years of Statistical Programming experience with early or late phase oncology trial studies.
BS/BA degree or other suitable qualification with relevance to the field.
Experience leading one or more statistical programming contractors, and programming vendors.
Proficiency in providing hands-on SAS Programming support for production or validation of analysis datasets, tables, listings and figures.
Demonstrated ability to multi-task, prioritize options, anticipate challenges, and execute goals as a member of an interdisciplinary team is extremely important.
Preferred Skills:
A demonstrable record of strong leadership and teamwork.
Thrives in a collaborative team setting and is driven by a desire to deploy innovative approaches and technologies in a high energy environment.
Experience working in a small to mid sized biotech/pharma environment.
Experience collaborating on development of processes, SOPs and guidance documents for the Statistical Programming function.ย
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