Executive Dir or Vice President, Biostatistics and Data Mgmt

Role OverviewThe Executive Director or Vice President, Biostatistics and Data Management (DM) functions is responsible for all aspects of DM and statistical planning, programming, analysis, and reporting for Savara. Provides direct management of all Savara DM team members as well as high-level oversight of all contract data managers and DM members from CROs. Responsible for identifying and managing all contract statistical CROs and consultants to ensure accurate and timely reporting of results from Savara clinical trials. Responsible for the management of DM and Biostatistics timelines and budgets. Core ResponsibilitiesOversight and high-level management of Savara and CRO DM tasks, resources, and timelines; day-to-day management is the responsibility of the Savara Director of Clinical DMLine management of the Director of Clinical DM, including oversight of responsibilities, evaluation of performance, and active support of professional goals/objectives/developmentSupport the DM team in the review of data for accuracy, quality, and interpretability, as neededOversight and management of all aspects of statistical planning, programming, analysis, and reporting for the company, including oversight and management of all contract statistical CROs and consultants and review and approval of statistical outputs, such as analysis datasets and tables/figures, and listings (TFLs)Serve as author, co-author, or primary reviewer and approver of SAPs, study data standardization plans (SDSPs), and statistical sections of documentsPerform statistical programming and analysis to validate key analysis datasets and TFLs and to provide statistical outputs for publication purposes or internal planning/decision-makingResponsible for the determination and monitoring of and necessary adjustments to the annual resourcing and budget for DM and biostatistics Lead role in authoring and/or reviewing the statistics-related sections of the protocol synopsis, clinical study protocols, and relevant sections of the Investigator’s Brochure (IB), regulatory documents, Clinical Study Report (CSR), and other critical clinical study documents, in close collaboration with the Study Responsible Physician (SRP) and in partnership with supporting departments within Savara Leverage scientific background to collect, translate, summarize and draft individual study concepts/strategies into study designs, in collaboration with the SRP, to drive protocol development and/or amendments Present data internally to stakeholders and externally to academic collaborators through presentations and contributions to publications Support interactions with relevant stakeholders and partners to facilitate successful conduct of clinical trials including clinical site personnel and CROs Provide statistical support to Regulatory Affairs activities for a clinical program (e.g., authoring or reviewing sections of Health Authority documents/responses; participate in Sponsor inspections)Collaboration with other members of the department led by the Chief Medical Officer in developing program strategies, planning resources, tracking progress on studies and submissions, and setting departmental objectives and priorities Represent Savara externally, as needed Other duties as assigned.Required QualificationsAdvanced degree in statisticsAt least 20 years (15 years if with PhD degree) of progressive experience in statistics as applied to clinical studies in the pharmaceutical, biotechnology, or CRO industryAt least 5 years of experience in the functional management of statistics and DM at the Senior Director level or higherHas served as lead statistician on Phase I-IV studies and New Drug Applications (NDAs), Biologics License Applications (BLAs), and/or Marketing Authorization Applications (MAAs) in various therapeutic areas Ability to manage external vendors for statistical and data management activitiesExpertise in SAS programming and in-depth knowledge of and practice in applying Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) standardsBroad knowledge and clear understanding of FDA requirements related to electronic systems and records; strong understanding of guidelines as they relate to DM and statistics, including Good Clinical Practice (GCP) and International Council on Harmonisation for Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines Work Schedule and LocationThis role is remote within the US and requires availability to work US Eastern Time Zone.Travel to Langhorne office as required for staff meetings and other important company meetings (estimated to be quarterly.Savara provides Comprehensive Benefits including:Highly competitive medical, dental, and vision coverageFlexible Spending Account for health care and dependent care expenses and Health Savings AccountPaid time off and paid holidays, including Dec 24-Jan 1Paid parental leave401(k) with highly competitive matchLife, AD&D, STD and LTD insurance coverageSavara’s compensation for this role will include a base salary, bonus, and equity. This role will be filled at the Executive Director of Vice President level. The base salary range for this role is $285,000 to $355,000.About SavaraSavara is a clinical stage biopharmaceutical company focused on rare respiratory diseases. The company's lead program, molgramostim nebulizer solution, is in Phase 3 development for autoimmune pulmonary alveolar proteinosis (aPAP). Savara's management team has extensive experience in rare respiratory diseases and pulmonary medicine, advancing product candidates to approval and commercialization.

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