Associate Director, Biostatistics

Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale. Our lead product candidate, lysergide tartrate (our proprietary orally disintegrating tablet form of lysergide (LSD) D-tartrate), represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges. Guided by the recognition that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address the underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today’s mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX. Together we are moving psychiatry forward—beyond better, into a boundless future. Join us! As an Associate Director, Biostatistics this person will provide statistical support for pipeline compounds’ clinical development, regulatory filing, and commercialization. Reporting to Vice President, Head of Biometrics and Data Science, the successful candidate will serve as the biostatistician for assigned clinical trials to provide statistical leadership from trial design, data analysis, to results interpretation and dissemination. This role will also provide statistical support to regulatory filing dossier preparation. As a hands-on biostatistician, this individual will be responsible for all statistical deliverables for the assigned projects in collaboration with members Biometrics team and in multi-functional project teams. Working closely with Definium Statistical Programming group, this individual will oversee the deliverables from statistical vendors to ensure high quality and meeting timeline. Additionally, the responsibilities of this individual include performing statistical analyses on trial data using SAS programs and partnering with the Clinical Data Management group to support data cleaning activities. Responsibilities Serve as Study Biostatistician for assigned clinical trials to provide statistical support from design, analysis to reporting Serve as the biostatistician conducting integrated data analyses to support regulatory filing dossier preparation Collaborate with cross-functional experts on clinical trial designs and make contributions to determination of objectives, endpoints and sample size Author statistical methods section in the protocol and review the protocol throughout Make certain the accuracy of randomization algorithm and contribute to eCRF design to ensure that study objectives, data analysis and data collection are aligned Work with statistical vendors and internal Statistical Programming team to deliver study results or integrated analyses with quality and speed Provide statistical input to any form of data reporting or external dissemination, including clinical study report, regulatory communication and publication Conduct data analyses as needed by using own SAS programs in collaboration with internal Statistical Programming team Qualifications and Skills: A PhD degree in Statistics, Biostatistics or relevant fields with at least 7 years’ working experience, or a Master’s degree in Statistics, Biostatistics or relevant fields with at least 10 years’ working experience, in pharmaceutical or biotechnology companies Solid statistical knowledge and experience in clinical trial design (early to late phase), data analysis, and reporting Rich experience in authoring study SAP and TFL shells and driving the review process to achieve consensus among review functions to deliver the final versions Extensive experience in managing statistical vendors to implement SAP and deliver study results with quality and speed Solid knowledge and extensive experience of using statistical computational languages, such as SAS, to perform data analysis Working knowledge of regulatory guidance relevant to clinical trials from design to analysis Demonstrated capacity of collaboration with Clinical Development, Clinical Operations, Regulatory Affairs, Data Science and other relevant functions to deliver common goals Strong organizational and project management skills; demonstrated interest in continued learning and growing Detail-oriented and hold high standards of excellence for their work products Deliver and communicate effectively in the work-from-home environment Excellent interpersonal skills and is a good team player Preferred Experience Experience in CNS drug development from clinical trials design to data analysis Experience in regulatory filing from integrated data analysis planning and execution to submission dossier preparation The starting base pay range for this position is $183,656.00 - $208,950.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee’s geographic location. Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including: 100% paid health benefits including Medical, Dental and Vision for you and your dependents 401(k) program with company match and vesting after the turn of the first month after your start date Flexible time off Generous parental leave and some fun fringe perks!

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