948# Associate Director, Biostatistics Permanent role (TA-Autoimmune and Inflammatory Diseases)_Remote

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  • Company ClinChoice
  • Employment Full-time
  • Location 🇺🇸 United States nationwide
  • Submitted Posted 1 week ago - Updated 2 hours ago
<p></p><p>&nbsp;</p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds...</span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is currently recruiting for a <strong>Associate Director of Biostatistics, Remote</strong>&nbsp;to join our client’s team in a permanent position—an exciting opportunity to lead impactful statistical strategy in a dynamic environment.</span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>This is a remote role, with a preference for candidates who can travel to the client’s SF Bay Area location once a month to meet the team.&nbsp;<br>This is a support role as study statistician</strong></span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">We are seeking an <strong>Associate Director of Biostatistics </strong>to provide statistical expertise and operational support across a variety of clinical activities with a focus on supporting early-stage and late-stage clinical programs. &nbsp;This role will serve as lead study statistician, collaborating with cross-functional teams to support clinical development and data-driven decision-making. The Associate Director will contribute hands-on to key deliverables, manage CROs, and provide guidance to junior team members.&nbsp;</span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Essential Responsibilities:</strong>&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Contribute to the statistical design and analysis of early and late phase clinical studies.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Apply advanced statistical methods and data visualization skills to clinical trial data summaries&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">and interpretations such as integrated safety and efficacy analyses for regulatory submissions.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Serve as the biostatistics representative on cross-functional teams, ensuring alignment of&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">statistical approaches with study and program objectives.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Provide input on study design, endpoint selection, and sample size planning.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Draft statistical analysis plans (SAPs) and support interpretation of results.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Ensure the quality and accuracy of statistical deliverables by independently generating the&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">statistical deliverables and/or independently reviewing and validating the statistical&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">deliverables generated by either CRO or internal statistical programming team.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Manage CROs and mentor junior staff or contractors as appropriate.&nbsp;</span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>The Ideal Candidate:&nbsp;</strong></span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Education:&nbsp;</strong></span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Ph.D. in Biostatistics with 6+ years of relevant industry experience, or Master’s with 8+ years&nbsp;</span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Experience&nbsp;</strong></span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Strong foundation in clinical trial design, statistical analysis, and regulatory guidelines.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Experience in publication work and/or analysis of real-world data preferred.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Proficiency in statistical programming (SAS and R).&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Immunology or related therapeutic area experience a plus.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Demonstrated ability to manage multiple priorities and work cross-functionally.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Experience with both early-stage and late-phase clinical trials in biotech/pharmaceutical industry is preferred.</span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Skills:&nbsp;</strong></span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Strong analytical thinking and attention to detail.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Excellent verbal and written communication skills.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Ability to work independently in a fast-paced, regulated environment.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Ability to manage deliverables with competing priorities and influence others effectively.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Strong organizational skills, with the ability to manage workflows and activities to meet&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">department timelines.&nbsp;</span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">• Collaborative mindset and ability to influence without authority.&nbsp;</span></p><p style="line-height: 1;">&nbsp;</p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>The Application Process</strong></span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step.&nbsp; Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.</span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Who will you be working for?</strong></span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>About ClinChoice</strong></span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong>Our Company Ethos</strong></span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.&nbsp;&nbsp; The success of these core values is evidenced by our below industry average turnover rates.</span></p><p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.</span></p><p style="line-height: 1;"><span class="ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak" style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong><br><span data-teams="true">#LI-TT1 #LI-Remote #Associate Director#Permanent</span><br></strong></span></p><p style="line-height: 1;">&nbsp;</p><p style="line-height: 1;">&nbsp;</p>

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