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Director Statistical Programming Jobs in Maryland

Emmes Group

Associate Biostatistician

Rockville, MD · On-site

Supports development of statistical analysis plans, other study plans and statistical programming ... At Emmes, your actions and hard work will have a direct impact on public health initiatives, both ...

Emmes

Associate Biostatistician

Rockville, MD · On-site +1

Supports development of statistical analysis plans, other study plans and statistical programming ... At Emmes, your actions and hard work will have a direct impact on public health initiatives, both ...

Emmes

Associate Biostatistician

Rockville, MD · On-site

$90 - $120/hr

Supports development of statistical analysis plans, other study plans and statistical programming ... At Emmes, your actions and hard work will have a direct impact on public health initiatives, both ...

New

Captivation Software

Test Engineer 3

Annapolis, MD · On-site

$130K - $270K/yr

Bachelor's degree in Math, Science, Engineering, Statistics, Engineering Management or related ... This position is open for direct hires only. We will not consider candidates from third party ...

Beyond SOF

CPPM Test Engineer (TE3)

Linthicum, MD · On-site

$150 - $200/hr

A Bachelor's degree in in Math, Science, Engineering, Statistics, Engineering Management or related ... directed. * Establish and maintain the Critical Operational Issues table within the RVTM with ...

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Showing results 21-40

All JobsStatistical Programming JobsDirector Statistical Programming JobsDirector Statistical Programming Jobs in Maryland

Director Statistical Programming information

See Maryland salary details

$149K

$271.9K

$333.9K

How much do director statistical programming jobs pay per year?

As of Sep 8, 2026, the average yearly pay for director statistical programming in Maryland is $271,894.00, according to ZipRecruiter salary data. Most workers in this role earn between $252,800.00 and $313,000.00 per year, depending on experience, location, and employer.

What is a director statistical programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

What does a director statistical programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.

What are the key skills and qualifications needed to thrive as a director statistical programming?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

How does a director statistical programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.
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Director Statistical Programming jobs near you
Infographic showing various Director Statistical Programming job openings in Maryland as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $271,894 per year, or $130.7 per hour.

Senior Director, Biostatistics

Supernus Pharmaceuticals, Inc.

Rockville, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 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:
To contribute to the Company's Clinical program by providing direction, insight, and hands-on management & leadership covering the statistical content and requirements for Phase 1 through 4 activities.
Essential Duties & Responsibilities:
  • Provides statistical support and expertise for all necessary activities in Development, specifically design of Phase 1-4 studies and programs.
  • Provides for the statistical content of clinical trials.
  • Provides team leadership for regulatory filings including integrated components.
  • Provides hand-on supports to all statistical deliverables.
  • Provides statistical leadership and insight to team as a senior member of the Clinical Development organization.
  • Interacts with FDA and other regulatory agencies in statistical aspects of study design and data analysis.
  • Works under limited supervision.
  • Assists with other duties as needed by the management.

Supervisory Responsibilities:
  • Builds statistical group (including the hiring of new staff and development of existing staff) in an efficient manner to accomplish corporate objectives and elevate overall statistical group's performance.
  • Leads and/or manages both in-house and CRO activities related to application of statistics to clinical trials data.
  • Leads in the development and review of SOPs related to statistics.
  • 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:
  • PhD (or equivalent) in Statistics or Biostatistics.
  • Excellent presentation, communication and management skills with attention to detail and accuracy.
  • 10+ years of pharmaceutical industry experience (6+ years in a pharmaceutical company or regulatory agency).
  • Major participation as the statistical lead in at least 1 NDA filing.
  • Proven ability to help design successful clinical trials.
  • Proven ability to independently develop and lead statistical components of several ongoing projects in Phase 1-4.
  • Proven ability to lead adaptive design, longitudinal data analysis, missing data handling and sensitivity analysis.
  • Experience with PK and PK/PD methods and clinical trial simulation a plus.
  • Fluent in SAS programming (including SAS macro) and familiarity with other statistical packages (e.g., PASS, nQuery Advisor, R).
  • Expert knowledge of FDA guidance related to statistics and statistical programming.
  • Knowledge of ICH/GCP rules and regulations.
  • Must be able to clearly articulate project needs and status to project team and upper management.
  • Excellent interpersonal and communication skills in English language (writing, speaking, comprehending).
  • Computer literate with proficiency of Microsoft Office package including Word, Outlook, Excel, and Adobe PDF.

Other Characteristics:
  • Ability to work independently and as part of a team and maintain high ethical standards of integrity and quality.
  • Ability to lead and manage direct reports and statistical group.
  • Ability of having an innovative and dynamic approach to work.
  • A self-starter able to work independently and also 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 $257,000 to $294,000. 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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