Associate Director, Statistical Programming

About Servier Servier in the U.S. is a Boston-based, commercial-stage biopharmaceutical company launched by Servier Group in 2018. As a privately held organization, Servier is uniquely positioned to advance cutting-edge science, tackle underserved therapeutic areas and make patients the focus of every strategic decision. Job DescriptionRole SummaryThe Associate Director, Statistical Programming leads statistical programming activities for multiple studies, an asset or an indication by performing hands-on programming or oversight of outsourced deliverables. This individual will ensure that the statistical programming processes and deliverables are aligned with regulatory requirements and internal procedures. The role will interact closely with the study statisticians and study team regarding statistical programming aspects.Primary ResponsibilitiesManage statistical programming deliverables on one or more assets or indications by managing study leads and oversee study activities and vendor oversight.Oversee development and quality control or oversight plan of analysis datasets and outputs for individual study as well as integrated analyses.Ensure study leads deliver high quality, traceability, reproducibility of study outputs and timeliness of statistical programming deliverables to meet expectations and regulatory requirements.Mentor statistical programmers with regards to programming activities and project management.Independently implement routine and non-standard analysis algorithms for assigned projects or studies.Collaborate with statisticians, local and CRO programmers to define and implement analysis requirements and perform sponsor oversight regarding data and analysis.Ensure an efficient collaboration with all members of the clinical study team.Ensure the statistical programming systems, processes and deliverables are aligned with the relevant regulatory requirements, for instance:Clinical study reporting, e.g. ICH E3Electronic records handling, e.g. Chapter 21 of the US Code of Federal Regulation - Part 11Electronic submission of clinical data to agencies, e.g. e-CTD guidance and CDISC SDTM and ADaM standards.Ensure that the datasets (SDTMs and ADaMs) are CDISC compliant.Support on the design of new statistical programming processes or optimization of existing ones to reach the best productivity, to ensure the best quality of the statistical outputs, and to reach the best customer satisfaction (internally and externally) with flexibility, reliability and responsiveness. Work with the portfolio programming lead to create forecasts for different studies and resource requirements.Other responsibilitiesParticipate in working groups (either inter department or cross functional).Participate in the preparation of audit/inspection and could interact with auditors/inspectors.Contribute to the establishment and maintenance of common formats and templates for key Programming documentation (e.g., standard CRF pages, Tables, Figures and Listings).Plan and track project activities, timelines across projects. Provide justification for planned resource needs. Seek to optimize resource utilization and capacity. Accurate plans, well-managed projects, capacity to apply extra resources in urgent situation.Education and Required SkillsMasters in Statistics, Engineering or relevant field required with a minimum of 8 years of experience in statistical programming or biostatistics in the Pharmaceutical/Biotechnology industry in clinical development desirableExperience with statistical programming in Oncology desirableProficient in SASGood knowledge of CDISC ADaM and SDTMStrong knowledge of relevant regulatory and data submission guidelinesStrong understanding of drug development, including knowledge of interfaces and interdependencies with other functionsSelf-directed, technically strong, expert regarding statistical programming processes, management of statistical programmers at study levelStrong study management skillsGood negotiation and issue resolution skillsAbility to organize team work and prioritize and balance concurrent tasks and responsibilities.Excellent time management skillsAbility to educate internal and external interfaces (CROs and contractors) on the statistical programming processes, and the underlying regulatory requirementsTravel and LocationSome domestic and international travel requiredOn-site in Boston (recommended 2-3 days hybrid) or 100% remote with occasional travel to BostonServier’s CommitmentServier is committed to modeling diversity, equity, and inclusion within the industry. We are dedicated to fostering an environment that maintains equitable treatment for all and we welcome applicants who are passionate, committed, and innovative individuals. We encourage candidates to apply to our open roles as we are always willing to consider experiences and skills beyond what is listed in the job description.All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.Salary RangeThe salary range for this role is $165,000-$200,000. An employee’s pay position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, and business or organizational needs. We may ultimately pay more or less than the posted range, and the range may be modified in the future. Employees in this position are also eligible for Short-Term and Long-Term incentive programs. Servier also offers a competitive and comprehensive benefits package that includes benefits such as medical, dental, vision, flexible time off (Servier provides unlimited sick time and flex time, and does not accrue time off), 401(k), life and disability insurance, recognition programs among other great benefits (all benefits are subject to eligibility requirements). For more information on our benefits, please visit this link.