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Senior Manager Statistical Programming Jobs in Reston, VA

Ra

Marketing Analytics Senior Manager

Washington, DC · On-site

Marketing Analytics Senior Manager Job Level: Senior Level This is what you will do.. You will be ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

Ra

Marketing Analytics Manager

Arlington, VA · On-site

Mid - Senior Level This is what you will do.. You will be using quantitative methods to assess the ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

Ra

Marketing Analytics Manager

Washington, DC · On-site

Mid - Senior Level This is what you will do.. You will be using quantitative methods to assess the ... Who is proficient in Applied Statistics/Econometrics, Statistical Programming, Database Marketing ...

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All JobsStatistical Programming JobsSenior Manager Statistical Programming JobsSenior Manager Statistical Programming Jobs in Reston, VA

Senior Manager Statistical Programming information

See Reston, VA salary details

$25K

$103K

$173.7K

How much do senior manager statistical programming jobs pay per year?

As of Sep 8, 2026, the average yearly pay for senior manager statistical programming in Reston, VA is $103,004.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,500.00 and $111,300.00 per year, depending on experience, location, and employer.

How does a senior manager statistical programming typically collaborate with cross-functional teams in clinical research projects?

A Senior Manager Statistical Programming plays a pivotal role in coordinating with biostatisticians, clinical data managers, and medical writers to ensure seamless data flow and analysis throughout clinical trials. They oversee programming teams to deliver statistical outputs, such as tables, listings, and figures, while maintaining compliance with regulatory standards. Regular meetings and clear communication are essential, as the Senior Manager must interpret project requirements and translate them into actionable programming tasks, ensuring timelines and quality standards are met. This collaborative environment fosters continuous learning and problem-solving, as cross-functional input is vital for addressing complex data challenges.

What are the key skills and qualifications needed to thrive as a senior manager statistical programming, and why are they important?

To thrive as a Senior Manager Statistical Programming, you need expertise in biostatistics, programming languages like SAS or R, and experience with clinical trial data, typically supported by an advanced degree in a quantitative field. Familiarity with regulatory requirements (e.g., CDISC standards), clinical data management systems, and project management tools is essential. Strong leadership, communication, and problem-solving skills help you lead teams and liaise with cross-functional stakeholders. These skills ensure accurate, compliant data analyses and effective team management for successful clinical trial outcomes.

What is the difference between Senior Manager Statistical Programming vs Statistical Programmer?

AspectSenior Manager Statistical ProgrammingStatistical Programmer
CredentialsBachelor's/Master's in Biostatistics, Computer Science, or related field; often with management experienceBachelor's or Master's in Biostatistics, Statistics, or related field
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms data analysis, programming, and validation tasks under supervision
Employer & Industry UsagePharmaceutical, biotech companies, CROs, clinical researchPharmaceutical, biotech, clinical research organizations

The main difference is that Senior Manager Statistical Programming oversees teams and manages projects, while Statistical Programmers focus on executing data analysis and programming tasks. The senior role involves leadership responsibilities, whereas the programmer role is more technical and task-oriented.

What are popular job titles related to Senior Manager Statistical Programming jobs in Reston, VA?

For Senior Manager Statistical Programming jobs in Reston, VA, the most frequently searched job titles are:

What job categories do people searching Senior Manager Statistical Programming jobs in Reston, VA look for?

The top searched job categories for Senior Manager Statistical Programming jobs in Reston, VA are:

Senior Manager Statistical Programming jobs near you
Infographic showing various Senior Manager Statistical Programming job openings in Reston, VA as of June 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $103,004 per year, or $49.5 per hour.

Manager, Statistical Programming

Rockville, MD • On-site

Supernus Pharmaceuticals, Inc.
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees
Learn more about Supernus Pharmaceuticals, Inc.external

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 11 days ago

Job description

Supernus Pharmaceuticals is an award-winning biopharmaceutical company with more than 30 years of experience in developing and commercializing products that treat central nervous system (CNS) diseases. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. We currently have 8 products in the market that are making a real impact on patient outcomes.
Job Summary:
The Manager of Statistical Programming will lead and support statistical programming activities for clinical projects conducted by Supernus Pharmaceuticals. This role ensures the timely delivery of high-quality clinical trials analysis deliverables by adhering to established standards and processes
Essential Duties & Responsibilities:
  • Oversees all statistical programming activities for an in-house clinical study, ensuring compliance with Supernus standards.
  • Reviews and provides input on Statistical Analysis Plans (SAPs) to ensure alignment with study objectives.
  • Develops Study Data Tabulation Models (SDTMs) and Arrangement of variables (ADaM) mapping specifications in accordance with CDISC SDTM Implementation Guides (SDTM IG).
  • Programs and validates SDTM and ADaM datasets using SAS programs.
  • Prepares SDTM and AdAm Submission packages, including, define.xml, Reviews guide, and annotated eCRF.
  • Generates and validates Tables, Figures, and listings (LTFs) according to approved specifications.
  • Validates outsourced datasets provided by vendors and performs ad hoc analyses as needed.
  • Contributes to the development and enhancement of programming standards and workflows.
  • Mentors and guides junior programmers to foster skill development and ensure quality deliverables.
  • Employee management responsibilities assigned as needed.
  • Performs other duties as assigned.

Supervisory Responsibilities:
  • Provides leadership and management in an effective manner consistent with Company Values towards defined Corporate Objectives.
  • Understands Company Policy and procedure to be able to guide direct reports appropriately.

Knowledge & Other Qualifications:
  • Bachelor's degree in Life Sciences, computer science, mathematics, statistics, or a related quantitative/analytical field with a minimum of five years of experience in a pharmaceutical/ Clinical Research organization industry, a master's degree in a related field with a minimum of three years of experience, or a PhD with one year of experience.
  • Proficiency in R is a plus.
  • Demonstrated ability to develop SAS programs and macros to create SDTM, ADaM, and TFLs.
  • Demonstrated ability to identify and solve moderately complex problems.
  • Working knowledge of CDISC standards with hands-on experience in generating define packages.
  • Familiarity with ICH guidelines and FDA guidance related to clinical study conduct and data submission.
  • Familiarity with statistical methods that apply to Phase I-IV clinical trials.
  • Excellent written and oral communication skills including grammatical/technical writing skills.
  • Excellent attention to detail and accuracy.

Other Characteristics:
  • Ability to work independently and as part of a team and maintain high ethical standards of integrity and quality.
  • Ability of having an innovative and dynamic approach to work.
  • A self-starter able to work independently but comfortable working in a team environment.
  • Ability to consistently exhibit Supernus Values in interactions with employees at all levels of the organization, vendors, customers and others.
  • Capable of performing other duties as assigned by Management.
  • Authorized to legally work in the United States without visa sponsorship.

Physical Requirements/Work Environment/Travel Requirements:
  • Sedentary work. Exerting up to 10 pounds of force occasionally and/or carrying objects. Sedentary work involves sitting most of the time.
  • The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer screen, iPad, or other electronic device; and extensive reading.
  • The worker is not substantially exposed to adverse environmental conditions.

Compensation:
At Supernus, we offer a competitive compensation package that reflects your experiences and contributions. The expected salary range for fully qualified candidates applying for this role is $100,000 to $130,000. This range is what the Company reasonably expects to offer for the position and is not reflective of the full compensation scale of the role. This range may be modified in the future. An individual's salary within the range is based on multiple factors, which may include and are not limited to education, relevant experience, knowledge, length of industry experience and organizational needs.
You also will be able to participate in a competitive benefits package, including but not limited to: health, dental, vision, paid time off, 401k company match, company paid life insurance and health and wellness benefits. The total compensation package for this position also includes other compensation elements such as stock equity awards, employee stock purchase programs and participation in our Company's discretionary annual bonus program.
Supernus Pharmaceuticals is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, disability, protected veteran status, age or any other characteristic protected by law.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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