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Manager Statistical Programming Jobs in Gaithersburg, MD

Root//Source

Software Test Engineer I

Annapolis Junction, MD · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

Bachelor's degree in Math, Science, Engineering, Statistics, Engineering Management, or related discipline (or four additional years of related experience may be substituted for Bachelor's degree)

Otsuka

Associate Director, Biostatistics

Rockville, MD · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Partner closely with Clinical Development, Clinical Pharmacology, Clinical Management, Regulatory Affairs, Data Management, and Statistical Programming. * Drive evidence-based decision-making through ...

Otsuka

Associate Director, Real World Data Science

Rockville, MD

$60K - $60K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... 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 ...

Red Drum

Test Engineers

Annapolis Junction, MD · On-site

... Science, Engineering, Statistics, Engineering Management, or related discipline • Current TS clearance plus Polygraph • 0 - 20 + years of experience Company : Red Drum provides software ...

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Showing results 41-60

All JobsStatistical Programming JobsManager Statistical Programming JobsManager Statistical Programming Jobs in Gaithersburg, MD

Manager Statistical Programming information

See Gaithersburg, MD salary details

$91.3K

$159.1K

$269K

How much do manager statistical programming jobs pay per year?

As of Aug 19, 2026, the average yearly pay for manager statistical programming in Gaithersburg, MD is $159,141.00, according to ZipRecruiter salary data. Most workers in this role earn between $135,100.00 and $172,900.00 per year, depending on experience, location, and employer.

What is a manager statistical programming?

A Manager Statistical Programming oversees a team of statistical programmers who support clinical trials and research by developing, validating, and maintaining statistical programs. They ensure compliance with regulatory requirements, manage project timelines, and collaborate with statisticians, data managers, and other stakeholders. This role requires strong programming skills in SAS or other statistical software, leadership abilities, and expertise in clinical data standards such as CDISC.

What are the typical daily responsibilities of a manager statistical programming?

As a Manager Statistical Programming, your daily responsibilities usually include overseeing a team of statistical programmers, coordinating the development and validation of statistical programs for clinical trial data analysis, and ensuring deliverables meet regulatory and company quality standards. You will often interact with biostatisticians, data managers, and clinical teams to align programming outputs with study goals. Additionally, you may review project timelines, allocate resources, mentor junior programmers, and contribute to process improvement initiatives. This multifaceted role requires balancing technical oversight with leadership and interdepartmental communication.

What are the key skills and qualifications needed to thrive in the manager statistical programming position, and why are they important?

To excel as a Manager Statistical Programming, you need a solid background in statistics, programming (such as SAS, R, or Python), and experience with clinical trial data management, often supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory guidelines (e.g., FDA, ICH), data standards such as CDISC, and certifications in relevant programming languages or clinical data processes are highly beneficial. Strong leadership, project management, and effective communication skills are essential for guiding teams and collaborating with cross-functional departments. These skills enable the manager to deliver high-quality statistical programming deliverables, ensure regulatory compliance, and drive team performance in a deadline-driven environment.

What are the most commonly searched types of Statistical Programming jobs in Gaithersburg, MD?

The most popular types of Statistical Programming jobs in Gaithersburg, MD are:

What are popular job titles related to Manager Statistical Programming jobs in Gaithersburg, MD?

For Manager Statistical Programming jobs in Gaithersburg, MD, the most frequently searched job titles are:

What job categories do people searching Manager Statistical Programming jobs in Gaithersburg, MD look for?

The top searched job categories for Manager Statistical Programming jobs in Gaithersburg, MD are:

What cities near Gaithersburg, MD are hiring for Manager Statistical Programming jobs?

Cities near Gaithersburg, MD with the most Manager Statistical Programming job openings:

Manager Statistical Programming jobs near you
Infographic showing various Manager Statistical Programming job openings in Gaithersburg, MD as of August 2026, with employment types broken down into 100% Full Time. Highlights an 58% In-person, and 42% Remote job distribution, with an average salary of $159,141 per year, or $76.5 per hour.

Senior Director, Biostatistics

Supernus Pharmaceuticals, Inc.

Rockville, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 20 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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