Director or Senior Director, Statistical Programming

<h3><strong>Who we are:</strong></h3> <p>Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years.&nbsp;</p> <p>&nbsp;</p> <h3><strong>How we work:</strong></h3> <ul> <li><strong>PIONEER</strong>: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.</li> <li><strong>COLLABORATE</strong>: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.</li> <li><strong>BELONG</strong>: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.</li> </ul> <p>&nbsp;</p> <h3><strong>How you’ll contribute:</strong></h3> <p>The Head of Statistical Programming is responsible for all statistical programming activities in the Clinical Development group.&nbsp; This person will support clinical trials, including technical and project leadership overseeing the quality and timely delivery of all statistical programming deliverables for studies or for submissions. This person will ensure the team develops, maintains, validates and runs quality SAS programs that access, visualize, analyze, and report clinical trial data, in accordance with statistical analysis plans, ICH guidelines, and applicable regulatory requirements. This position will also include people management responsibilities for statistical programmers.</p> <ul> <li><strong>Leadership and Management:</strong> Lead the Statistical Programming team by providing strategic guidance, professional development, and motivation. Oversee the recruitment, training, and performance evaluation of team members.</li> <li><strong>Vendor Management:</strong> Manage relationships with Contract Research Organizations (CROs) to ensure they meet project timelines and quality standards.</li> <li><strong>Programming and Technical Oversight:</strong> Ensure the development and compliance of project/study-specific programming standards and specifications aligned with regulatory guidelines.</li> <li><strong>Data Standards and Analysis:</strong> Manage the creation of SDTM and ADaM datasets, ensuring compliance with CDISC standards, and oversee the programming of tables, listings, and figures (TLFs) according to statistical analysis plans.</li> <li><strong>Quality Control:</strong> Perform and oversee quality control checks on all programming deliverables to ensure accuracy and consistency.</li> </ul> <ul> <li><strong>Regulatory Submissions:</strong> Lead the preparation and review of datasets and documentation for regulatory submissions, ensuring compliance with all applicable regulatory requirements.</li> </ul> <ul> <li><strong>Innovation and Process Improvement:</strong> Initiate and implement innovative solutions for programming efficiency, including but not limited to the development of SAS macros.</li> </ul> <p>&nbsp;</p> <h3><strong>Skills and experience you’ll bring:</strong></h3> <ul> <li>Minimum of 10 years in statistical programming within the pharmaceutical or biotech industries, with a proven track record in a leadership role.</li> <li>Advanced skills in SAS programming (Base SAS, SAS/STAT, SAS/GRAPH), including macro development. Familiarity with other statistical software such as R and Python is strongly preferred.</li> <li>Deep understanding of clinical trial processes, data standards (CDISC, SDTM, ADaM), and regulatory submission requirements.</li> <li>Demonstrated ability to effectively lead and motivate a team, manage multiple projects, and work collaboratively across functions.</li> <li>A strong passion for innovation in statistical programming and continuous improvement in processes.</li> </ul> <p>&nbsp;</p> <h3><strong>Skills and experience not an exact match?:</strong></h3> <p>Go ahead and submit your resume (and a cover letter, if you’d like!).&nbsp; If this role isn't right for you, we can keep you in mind for future opportunities.</p> <p>&nbsp;</p> <p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</p> <p>&nbsp;</p> <p><strong><em><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">Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.&nbsp; All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.</span></em></strong></p> <p>&nbsp;</p>