Associate Director of Statistical Programming
Harvard University
Company DescriptionBy working at Harvard University, you join a vibrant community that advances Harvard's world-changing mission in meaningful ways, inspires innovation and collaboration, and builds skills and expertise. We are dedicated to creating a diverse and welcoming environment where everyone can thrive.Why join the Harvard T.H. Chan School of Public Health?The Harvard T.H. Chan School of Public Health is a world-renowned institution dedicated to advancing public health through cutting-edge research, education, and global collaboration. Our school is a special place to work because of its vibrant, mission-driven community, interdisciplinary approach, and commitment to addressing some of the most pressing health challenges worldwide. We foster a collaborative and inclusive work environment where innovation, continuous learning, and work-life balance are valued.Learn more about the School’s mission, objectives, and core values, our Principles of Citizenship, and about the Dean’s AAA vision about our school’s ongoing strategic initiatives.Job DescriptionJob Summary:The Center for Biostatistics in AIDS Research (CBAR), an organization within the Harvard T.H. Chan School of Public Health, is responsible for the design, monitoring and statistical analysis of clinical trials and observational studies for several major national and international NIH-funded clinical research networks. CBAR employs over 60 statisticians and epidemiologists including Harvard faculty, research scientists, and staff. Investigators within CBAR have provided statistical leadership and support for clinical research networks for thirty-five years. Currently this includes infectious disease networks such as: Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections (ACTG) and the International Maternal Pediatric Adolescent AIDS Clinical Trials Network (IMPAACT). Results from studies have helped to establish the paradigm for the treatment and prevention of HIV and other infectious diseases, and contributed to international treatment and prevention guidelines.This position is located in the Center for Biostatistics in AIDS Research (CBAR) within the Harvard T.H. Chan School of Public Health in Boston, Massachusetts. Since 1989, CBAR and the Harvard T.H. Chan School of Public Health have provided a strong program for growth and professional development of its research staff -- including a defined career path and opportunities for continuing education and attendance of professional meetings.CBAR has a hybrid work environment which includes a combination of on-campus/in-person work and remote work.Job-Specific Responsibilities: Reporting directly to the Director of Statistical Programming and AI Applications, the Associate Director of Statistical Programming is responsible for leading the statistical programming efforts for a busy research center. The individual will be responsible for collaborating with CBAR Leadership, project PI's, biostatisticians, and Core programmers as well as the CBAR Quality Management Team, IT professionals, Internal Resource Committees, external collaborators, and other colleagues in the creation, implementation, and maintenance of statistical programming infrastructure and deliverables. The Associate Director will lead the effort to continuously improve programming processes to conform to evolving industry standards and participate in the ongoing review and development of quality systems and processes, including CDISC implementation, R programming, AI integration, and other internal/external initiatives.The Associate Director will manage the priorities and expectations of the CBAR Programming Core comprised of approximately 10 programmers who design and implement expert applications (including SAS macros, R packages, and BASH scripts) supporting protocol-specific statistical programming and project priorities for Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections (ACTG) and the International Maternal Pediatric Adolescent AIDS Clinical Trials Group (IMPAACT). This includes high-level programming projects, including SAS, R, BASH, and Python, and ad hoc protocol-specific programming requests. As the process owner for Core Applications, the Associate Director is responsible for timely review and final approval of program specifications and requirements.The Associate Director will directly supervise programming managers and other senior Core programming staff. Responsibilities include personnel decision making at all levels of the Core, including hiring, promotion recommendations, and disciplinary actions. This position mentors programming staff and coordinates with the CBAR Training Committee with respect to the training needs of masters and doctoral-level statisticians and epidemiologists.This individual must possess extensive experience and proven skills in the use of SAS within a Statistical Programming environment and complete knowledge and understanding of the statistical programming processes, procedures, and roles. This individual will use knowledge of CDISC SDTM and ADaM standards to provide support Biostatistics in statistical analysis, both directly, and in the development of programming tools to streamline study-specific programming. Applicants with experience in R both SAS and R will be strongly preferred. Additionally, the successful candidate will use their strong people management skills and supervisory skills to provide direct line management to the statistical programmers, identify training needs and opportunities for optimizing staff utilization and employing the most efficient practices.Duties and responsibilities include, but are not limited to, the following:Signatory for CBAR Programming SOPs with responsibility for document revisions, CAPA management, response to internal audit, statistical programming representative for external audit/inspectionLead Programming Core priorities and commitments, including assessment of new applications, needs of statistics and requirements, allocation of resources including for ad-hoc projects, review, and final approval of program specifications and requirementsManage, cultivate, and establish requirements for a pipeline of statistical programming projects. Projects may include macro and script development to support the work of biostatistics teams, study-specific work, standardization efforts, ad-hoc projects, etc.Directly supervise the Manager of Programming Systems, the Manager of Programmer Development, and the Manager of Data Standardization providing oversight for advanced application design and planning, Core programmer training, and clinical data standardization, respectivelyCollaboration with the CBAR IT team to ensure thorough and smooth testing associated with critical hardware and software updatesPrimary liaison with the ACTG/IMPAACT Data Management Center in Amherst, NY; responsible to ensure the harmonization of programming systems and deliverables between the two organizations;Supporting statisticians and epidemiologists with external collaborators to ensure efficient and secure data transferCoordination with the CBAR Training Committee with respect to the training needs of master- and doctoral-level statisticians and epidemiologistsOther duties as assignedPlease attach the following when applying: 1) Resume, 2) Cover letter, 3) Sample of SAS Code (solely created by the applicant - preferably utilizing macro language), and 4) Names and email addresses for three (3) Professional references.PLEASE NOTE: This position has a term date of November 30, 2027 with a strong likelihood of extension.QualificationsBasic Qualifications:Minimum of 7 years’ post-secondary education or relevant work experience is requiredSupervisory experience is requiredAdditional Qualifications and Skills: The following job-related skill and experience is strongly preferred, but not required:Bachelor’s or Master’s Degree in Mathematics, Statistics, Computer Science, or related fieldExperience working with all levels of management and consulting with key business stakeholdersAn aptitude to influence for greater outcomesProven leadership skills with prior management and extensive supervisory experienceProven history of managing programming capability and projects in a research settingExperience with SAS, R, Bash, Linux, and Python are highly desirableAt least seven years of high-level statistical programming skills in a clinical data environment or research setting, preferably with clinical trial dataProven skills in the use of SAS and a scripting language within a Statistical Programming environment, preferably with clinical trial data (knowledge of R is desirable)Strong team player that has a customer service approach and is solution-orientedAttention to detail and can work individually, within a multi-disciplinary team, as well as with external partners and vendorsStrong written and verbal communication skills; technical writing experience is desirableAdditional InformationAppointment End Date:November 30, 2027Standard Hours/Schedule: 35 hours per weekVisa Sponsorship Information: Harvard University is unable to provide visa sponsorship for this positionPre-Employment Screening: Identity, EducationJoin the Harvard T.H. Chan School of Public Health to support our mission of health research and education, and to be a part of the oldest institution of higher learning in the country!--------------------The Harvard T.H. Chan School of Public Health does not provide visa sponsorship, now or in the future, for staff positions.Harvard University requires pre-employment reference checks and background screenings.This position has a 180 day orientation and review period. --------------------The health of our workforce is a priority for Harvard University. With that in mind, we strongly encourage all employees to be up to date on CDC-recommended vaccines.Work Format DetailsThis position has been determined by school or unit leaders that some of the duties and responsibilities can be effectively performed at a non-Harvard location. The work schedule and location will be set by the department at its discretion and based upon operational needs. When not working at a Harvard or Harvard-designated location, employees in hybrid positions must work in a Harvard registered state in compliance with the University’s Policy on Employment Outside of Massachusetts. Additional details will be discussed during the interview process. Certain visa types and funding sources may limit work location. Individuals must meet work location sponsorship requirements prior to employment.Salary Grade and RangesThis position is salary grade level 059. Please visit Harvard's Salary Ranges to view the corresponding salary range and related information.BenefitsHarvard offers a comprehensive benefits package that is designed to support a healthy work-life balance and your physical, mental and financial wellbeing. Because here, you are what matters. Our benefits include, but are not limited to:Generous paid time off including parental leaveMedical, dental, and vision health insurance coverage starting on day oneRetirement plans with university contributionsWellbeing and mental health resourcesSupport for families and caregiversProfessional development opportunities including tuition assistance and reimbursementCommuter benefits, discounts and campus perksLearn more about these and additional benefits on our Benefits & Wellbeing Page.EEO/Non-Discrimination Commitment StatementHarvard University is committed to equal opportunity and non-discrimination. We seek talent from all parts of society and the world, and we strive to ensure everyone at Harvard thrives. Our differences help our community advance Harvard's academic purposes.Harvard has an equal employment opportunity policy that outlines our commitment to prohibiting discrimination on the basis of race, ethnicity, color, national origin, sex, sexual orientation, gender identity, veteran status, religion, disability, or any other characteristic protected by law or identified in the university's non-discrimination policy. Harvard's equal employment opportunity policy and non-discrimination policy help all community members participate fully in work and campus life free from harassment and discrimination.SummaryType: Full-timeFunction: Information TechnologyExperience level: Not ApplicableIndustry: Higher Education
- ...for the design, monitoring and statistical analysis of clinical trials... ...Health have provided a strong program for growth and professional... ...Responsibilities: Reporting directly to the Director of Statistical Programming and AI Applications, the Associate Director of Statistical...SuggestedWork experience placementRemote workWorldwide
- Job DetailExperience Level Associate DirectorDegree Type Master of Science (MS)Employment... ...Points Lead impactful statistical programming initiatives in a hybrid work environment... ...advancements.Job DescriptionAssociate Director of Statistical Programming OverviewThe...SuggestedWork at officeRemote work
- Kymera Therapeutics is seeking an experienced Associate Director or Director of Statistical Programming to lead the programming efforts for a compound-level program across multiple clinical studies. The role requires ensuring high-quality, timely, and regulatory-compliant...Suggested
$172k - $258k
...area of Boston, Massachusetts.SummaryTango has an exciting opportunity to join our growing Biostatistics team as an Associate Director, Statistical Programming, reporting to the Senior Director of Statistical Programming. In this role, you will be responsible for study-...Suggested$181.1k - $244.9k
The Associate Director, Statistical Programming is responsible for statistical programming activities in support of clinical trials including technical and project leadership overseeing the quality and timely delivery of all statistical programming deliverables for studies...SuggestedFull timeTemporary workLocal areaFlexible hours$172k - $258k
...Associate Director, Statistical Programming Company Overview Tango Therapeutics is a clinical-stage biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer. Using an...For contractors$160k - $275k
..., seen, and heard. How you’ll make an impact: Kymera Therapeutics is seeking an experienced and strategic Associate Director or Director of Statistical Programming to lead programming efforts for a compound-level program spanning multiple clinical studies. This role will...$198.16k - $216.2k
...Tyra Biosciences, Inc. is seeking a highly motivated Associate Director, Statistical Programming, to make impactful contributions to projects targeting disease areas with high unmet medical needs. The successful candidate will be highly organized, self-motivated, and thrive...Full timeTemporary workFor contractorsWork at officeRemote workFlexible hours- ...Tango Therapeutics, a Boston-based clinical-stage biotechnology company, is seeking an Associate Director, Statistical Programming to join the Biostatistics team. You will lead study-specific programming activities, maintain analysis datasets (SDTM/ADaM), and ensure SOP...
- ...Tango Therapeutics seeks an Associate Director of Statistical Programming to lead clinical trial programming activities, manage analysis datasets and regulatory submissions, and oversee statistical computing infrastructure. The role reports to the Senior Director and requires...
- ...Damora Therapeutics, Inc. in Boston, MA seeks a Head of Statistical Programming to lead the programming function across its clinical portfolio. You will define strategy, manage internal staff and CROs, and ensure regulatory-ready programming deliverables. The role requires...
$184.07k - $198.8k
The Associate Director of Statistical Programming, as a member of the Biostatistics & Statistical Programming Department, will contribute to Alkermes to achieve the goals of continuing growth in neuroscience. The Associate Director will combine technical and project management...Work at officeLocal areaFlexible hours3 days per week$171.5k - $214.42k
...progression in Multiple Sclerosis (MS). Zenas’ earlier stage programs include ZB021, a clinical-stage, potentially best-in-... ...Excellence and Innovation - TRUE Innovation!Position Summary:The Associate Director, Statistical Programming will independently lead and execute...Contract workFlexible hours- ...cancers with significant unmet need. The company’s lead program, DMR-001, is an investigational monoclonal antibody designed... ...-ready data across its pipeline. Position Summary The Associate Director, Statistical Programming serves as the programming lead for one or more...For contractors
$200.7k - $271.5k
Overview:The Director, Technical Solutions will be responsible for defining and executing... .... This leader will oversee AWS-based programming and analytics platforms, drive innovation... ...of the AWS cloud platform supporting Statistical Programming, Biostatistics, Epidemiology...Full timeTemporary workLocal areaFlexible hours- ...Kymera Therapeutics seeks an experienced Associate Director or Director of Statistical Programming to lead programming efforts across multiple clinical studies for a targeted protein degradation compound. This role requires strategic oversight of in-house and external...
- ...Rapport Therapeutics seeks a Senior Manager/Associate Director of Statistical Programming to lead clinical trial programming activities across the Bipolar Mania program. The role involves overseeing SAS programming deliverables, managing CRO partnerships, and ensuring...
- ...Director, Technical Solutions – Statistical Programming Location: Cambridge, MA (Local candidates or those willing to relocate) Industry: Pharmaceutical / Biotechnology Employment: Full-Time, Permanent Position Overview We are seeking an experienced Director of Technical...Permanent employmentFull timeLocal areaRelocation
- ...Kymera Therapeutics, Inc. in Boston seeks an experienced Associate Director or Director of Statistical Programming to lead programming for a compound-level program across multiple clinical studies. This role emphasizes strategic leadership, hands-on programming, and collaboration...
$132k - $172k
...common goal of elevating science and service for rare patients. Position Summary: The Senior Manager, Statistical Programming will work closely with the Associate Director, Statistical Programming and other members of the Biometrics team to provide programming support...Temporary workFor contractorsRemote work$128.6k - $210k
.... A Manager provides timely support to the study team on all programming matters according to the project strategies. As an integral part... ...studies. Requirements will be identified according to a Statistical Analysis Plan, programming specification or user requirements...Permanent employmentFor contractorsWork experience placement- ...culture where every voice is heard, and where our shared mission unites us across functions and geographies. Senior Manager, Statistical Programming Position Summary The Senior Manager, Statistical Programming will provide hands‑on statistical programming leadership and...Worldwide
$128.6k - $210k
...use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead...Permanent employmentFor contractorsWork experience placementWorldwideShift work- ...Vor Biopharma seeks a Senior Manager of Statistical Programming to lead SAS programming efforts for clinical studies evaluating an autoimmune disease therapy. The role involves designing and validating statistical programs, managing study datasets, and collaborating across...
$128.6k - $210k
...Regeneron seeks a Manager, Statistical Programming to lead programming deliverables for clinical studies from initiation through regulatory approval and product launch. The role involves managing programming teams, developing analytical outputs, and serving as a programming...- ...Vor Biopharma is seeking a Senior Manager, Statistical Programming to lead and deliver high-quality programming for complex clinical studies. You will drive SDTM/ADaM data development, ensure regulatory-ready outputs, and mentor junior programmers while partnering with...
- ## Sr. Manager, Statistical ProgrammingApplylocations: Paris: Cambridge One Main: Londontime... ...1927**Title:**Sr. Manager, Statistical Programming**Company:**Ipsen Innovation (SAS)**... ...tables, listings, figures, datasets, and associated documentation, e.g. DEFINE.XML. Participate...
- ...Tango Therapeutics, Inc. is seeking an Associate Director, Statistical Programming to lead and manage programming activities for clinical trials. The role develops SDTM/ADaM datasets and TLFs, validates analyses, and supports regulatory submissions under CDISC standards...
$193.1k - $289.7k
Job DescriptionGeneral Summary:The CMC Statistics Director (Scientific Fellow) provides strategic and technical leadership for the application... ...analysisProvide advanced statistical support for stability programs, shelf-life estimation, comparability assessments, and...Full timeSummer workRemote workFlexible hours2 days per week$169.4k - $266.2k
...9,400.00 - $266,200.00Company: Takeda PharmaceuticalsPosted: 2026-10-02Job TitleJob DescriptionObjective/Purpose:Provide strategic program leadership at the asset level for complex Medical priorities, ensuring that TA and asset strategies are translated into executable...Minimum wageTemporary workLocal area
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Associate Director of Statistical Programming. Be the first to apply!
- associate director operations Boston, MA
- associate director Boston, MA
- associate scientific director Boston, MA
- remote associate product manager Boston, MA
- associate director contracts Boston, MA
- associate manager digital marketing Boston, MA
- associate media director Boston, MA
- associate program manager Boston, MA
- associate clinical manager Boston, MA
- associate director communications Boston, MA




