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Associate Director Statistical Programming Jobs in Washington

The Research Methodologist reports to the Associate Director for U.S. Survey Methods and works ... Strong proficiency programming in the R statistical programming language is required. (Beginner ...

DC News Now is seeking a skilled Associate Director / Director to join our production team. This ... Direct live newscasts, breaking news, and special programming using broadcast automation systems ...

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Associate Director Statistical Programming information

See Washington salary details

$173.9K

$317.3K

$389.6K

How much do associate director statistical programming jobs pay per year?

As of May 30, 2026, the average yearly pay for associate director statistical programming in Washington is $317,294.00, according to ZipRecruiter salary data. Most workers in this role earn between $295,000.00 and $365,300.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Associate Director Statistical Programming, and why are they important?

To thrive as an Associate Director Statistical Programming, you need expertise in statistical programming, clinical trial data standards, and a degree in statistics, mathematics, or a related field, often with several years of experience in the pharmaceutical or biotechnology industry. Proficiency in programming languages such as SAS and R, knowledge of CDISC standards (SDTM, ADaM), and familiarity with regulatory submission requirements are typically required. Strong leadership, project management, and communication skills are vital for guiding teams and collaborating with cross-functional partners. These skills and qualities ensure the delivery of high-quality, compliant statistical outputs that support clinical development and regulatory approval.

How does an Associate Director of Statistical Programming typically collaborate with cross-functional teams in a pharmaceutical or biotech setting?

As an Associate Director of Statistical Programming, you will work closely with biostatisticians, clinical data managers, and regulatory affairs professionals to ensure that statistical analyses and data outputs meet project and regulatory requirements. You’ll often lead programming teams, coordinate timelines, and help translate statistical analysis plans into executable code. Regular meetings and clear communication are key, as you’ll be expected to provide technical guidance and ensure data integrity across multiple studies or programs. This role often requires balancing hands-on programming with strategic leadership and mentorship responsibilities.

What does an Associate Director of Statistical Programming do?

An Associate Director of Statistical Programming leads teams responsible for the design, development, and validation of statistical programs used in the analysis of clinical trial data. They oversee the creation of datasets, tables, listings, and figures that support regulatory submissions and scientific publications. In addition to technical expertise, this role involves managing timelines, ensuring compliance with regulatory standards, and collaborating with cross-functional teams such as biostatistics, data management, and clinical operations.

What is the difference between Associate Director Statistical Programming vs Statistical Programmer?

AspectAssociate Director Statistical ProgrammingStatistical Programmer
Required CredentialsBachelor's or Master's in Biostatistics, Statistics, or related field; experience in clinical trial programmingBachelor's or Master's in similar fields; entry to mid-level experience
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms programming tasks, supports project teams, executes statistical analyses
Employer & Industry UsagePharmaceutical and biotech companies, clinical research organizationsPharmaceutical companies, CROs, biotech firms

The Associate Director Statistical Programming typically oversees programming teams and manages project deliverables, requiring leadership skills and extensive experience. In contrast, the Statistical Programmer focuses on executing programming tasks under supervision. Both roles are essential in clinical research, but the Associate Director holds more managerial responsibilities and strategic oversight.

What are popular job titles related to Associate Director Statistical Programming jobs in Washington? For Associate Director Statistical Programming jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Associate Director Statistical Programming jobs in Washington look for? The top searched job categories for Associate Director Statistical Programming jobs in Washington are:
What cities in Washington are hiring for Associate Director Statistical Programming jobs? Cities in Washington with the most Associate Director Statistical Programming job openings:
Associate Director, Real World Data Science

Associate Director, Real World Data Science

Otsuka

Rockville, MD

$60.10K - $60.60K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago


Job description

The Associate Director of Real-World Data Science is an expert in analysis and methods, providing leadership within Otsuka's OPDC, reporting to the Data and Analytics team. This position demands expertise in research design, and data analysis, including traditional and AI/ML methodologies, that can be applied to health economics research. A visionary approach to managing and optimizing research Real World Data, platforms, processes, and data systems is desired. The successful candidate will possess advanced skills in health economics research, programming and data analysis, focusing on leveraging large healthcare datasets, including claims, electronic health records (EHR), and clinical trial data, data linking/ tokenization, to support value evidence generation.

The responsibilities for this role include collaborating closely with Value Evidence (VE) team and across therapeutic areas to execute HEOR projects and strategies, encompassing pharmaceuticals, devices, and digital health solutions using traditional as well as novel data sources and methodologies. The Associate Director will support successful execution through robust data analyses, project management, and dissemination of HEOR and real-world evidence, late-stage studies to stakeholders. Additionally, the role is critical in producing high-quality research and data to enhance the scientific understanding and the potential value and real-world impact of Otsuka products for payers, healthcare providers, patients, and caregivers.

Responsiblities include:

  • Strategic Leadership: Partner with Value Evidence Strategy to design and lead analytical studies and programming for RWE analysis plans to support value and scientific evidence generation.
  • Cross-Functional Collaboration: Work closely with Value Evidence and Global Medical Affairs teams to support value and scientific evidence generation across Otsuka's product portfolio.
  • Data Analysis and Innovation: Apply fit for purpose traditional or novel methodologies, including AI/ML methodologies, in data and statistical techniques, stay current with new analytical approaches, and collaborate with subject matter experts to design and deliver medically relevant and scientifically valid projects.
  • Protocol Development: Co-lead study protocol development and database query guidelines for internal dataset, overseeing internal analyses to support studies.
  • Pharmacoeconomic Support: Serve as the interface to support pharmacoeconomic and real-world data needs across various departments.
  • Study Management: Co-lead in the preparation and review of study protocols and reports for internal datasets, including statistical analysis plans, and manage associated vendors as appropriate.
  • Data Licensing and Vendor Oversight: Manage department-specific data licensing and platform needs, overseeing vendors and ensuring compliance with licensing terms.
  • Database Identification: Identify appropriate databases (US and ex-US) for licensing to address research questions and align with therapeutic area strategy.
  • External Partnerships: Participate in establishing external partnerships and work on all scientific aspects of projects involving these partnerships.
  • Presentation and Communication: Present analytics for health outcomes projects and information to internal and external groups, including regulatory authorities, key opinion leaders, and at medical and outcomes research conferences.
  • Publications: Participate in publication planning and execution, coordinating with Otsuka Scientific Communications personnel and VES.
  • Advisory Meetings: Support preparation of medical or payer advisory meetings to solicit feedback on Otsuka products and therapeutic areas.
  • Project Execution: Identify and support projects that directly support the economic and quality strategy for Otsuka products.
  • Formulary Submissions: Support in the development of product dossiers and other projects to support different aspects of formulary submissions.
  • Budget Management: Manage budget resources allocated to assigned projects.
  • Education and Awareness: When appropriate, assist in developing educational material for internal and external audience including payer communication field tools.
  • Compliance and Best Practices: Maintain awareness of current strategies, issues, and new data sources, ensuring compliance with all guidelines and best practices for scientific research.

Qualifications/ Required

Knowledge/ Experience and Skills:

  • Experience and Expertise:3-5 years of experience in outcomes research methods and analysis, with strong expertise in non-interventional study designs and statistical analyses.
  • Industry Knowledge:Comprehensive understanding of the healthcare industry, including pharmaceutical R&D, clinical research, commercialization, health technology assessment bodies, managed care marketplace, hospital systems, and integrated systems of care.
  • Technical Skills:Proficiency in statistical programming (SAS and AWS environment required; R preferred), with experience in ML/AI applications.
  • Research and Analytical Skills:Ability to independently develop research hypotheses, study protocols, and statistical analysis plans, with knowledge of epidemiology, economics, psychometrics, and medical writing.
  • Data Utilization:Strong understanding of administrative claims data, electronic medical records, hospital inpatient data, and survey data, including their applications and limitations.
  • Project Management:Proven ability to manage complex projects involving multiple external vendors, with excellent project management skills.
  • Interpersonal and Communication Skills:Excellent interpersonal skills, superior presentation skills, and the ability to manage conflict constructively with minimal supervision.
  • Stakeholder Engagement:Experience working with and overseeing external contractors and vendors, with the ability to understand and respond to customer/payer requests and develop value dossier
  • Travel Requirements:Willingness to travel approximately 10%, including international travel, for conferences, corporate locations, and stakeholder meetings.

Educational Qualifications:

  • PhD or Masters in Health Economics, Outcomes Research, Health Services Research, Public Health or related discipline
  • Three (PhD) to five (Masters) years of relevant experience

Competencies
Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
Strategic Thinking & Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the business.
Patient & Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
Impactful Communication -Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
Respectful Collaboration - Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals.
Empowered Development - Play an active role in professional development as a business imperative.

Minimum $169,222.00 - Maximum $253,000.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate's job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.

Application Deadline: This will be posted for a minimum of 5 business days.

Company benefits: Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.

Come discover more about Otsuka and our benefit offerings;https://www.otsuka-us.com/careers-join-otsuka.

Disclaimer:

This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.

Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.

If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request.

Statement Regarding Job Recruiting Fraud Scams

At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.

Please understand, Otsuka will never ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.

Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.

To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website https://vhr-otsuka.wd1.myworkdayjobs.com/en-US/External.

Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka's call center at: 800-363-5670. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: https://www.ic3.gov, or your local authorities.

Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. ("Otsuka") does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka's application portal without a valid written search agreement in place for the position will be considered Otsuka's sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.