
Associate Director, Biostatistics
Posted Jul 22

Posted Jul 22
This is a fully remote position, open to applicants in California.
• Collaborate with cross-functional study and project teams to support hematology studies.
• Create and execute the statistical analysis plan (SAP) for the clinical study report (CSR).
• Evaluate data and interpret outcomes from clinical trials to achieve the objectives outlined in the study protocol.
• Prepare both oral and written reports to effectively convey the results of clinical trials.
• Address inquiries related to study design, analysis, and interpretation from clinical monitors, regulatory agencies, and/or investigators.
• Participate in research initiatives focused on innovative statistical methodologies.
• A minimum of a PhD in Statistics or a related field with over 5 years of experience, or a Master’s degree accompanied by at least 8 years of experience in clinical drug development.
• Proficiency in SAS and/or R.
• Experience with clinical trials and familiarity with regulatory guidelines are essential.
• Oncology experience is preferred but not mandatory.
• Proven written and verbal communication skills.
• Capability to work collaboratively within a team as well as independently.
• Medical
• Dental
• Vision
• 401(k)
• FSA/HSA
• Life Insurance
• Paid Time Off
• Wellness
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