ZipRecruiter

Log In

1

Director Statistical Programming Jobs in Silver Spring, MD

Beyond SOF

CPPM Test Engineer (TE3)

Linthicum, MD · On-site

$135 - $165/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 ...

previous pagenext page

Showing results 21-40

All JobsStatistical Programming JobsDirector Statistical Programming JobsDirector Statistical Programming Jobs in Silver Spring, MD

Director Statistical Programming information

See Silver Spring, MD salary details

$158.7K

$289.6K

$355.6K

How much do director statistical programming jobs pay per year?

As of Sep 4, 2026, the average yearly pay for director statistical programming in Silver Spring, MD is $289,610.00, according to ZipRecruiter salary data. Most workers in this role earn between $269,300.00 and $333,400.00 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.
More about Director Statistical Programming jobs

What are popular job titles related to Director Statistical Programming jobs in Silver Spring, MD?

For Director Statistical Programming jobs in Silver Spring, MD, the most frequently searched job titles are:

What job categories do people searching Director Statistical Programming jobs in Silver Spring, MD look for?

The top searched job categories for Director Statistical Programming jobs in Silver Spring, MD are:

What cities near Silver Spring, MD are hiring for Director Statistical Programming jobs?

Cities near Silver Spring, MD with the most Director Statistical Programming job openings:

Director Statistical Programming jobs near you
Infographic showing various Director Statistical Programming job openings in Silver Spring, MD as of August 2026, with employment types broken down into 100% Full Time. Highlights an 69% In-person, 8% Hybrid, and 23% Remote job distribution, with an average salary of $290,165 per year, or $139.5 per hour.

Associate Director Biostatistics

Emmes Group

Rockville, MD • On-site

Full-time

Medical, Retirement

Posted 22 days ago

Job description

Overview
Associate Director, Biostatistics
US Remote
Emmes Group: Building a better future for us all.
Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.
We believe the work we do will have a direct impact on patients' lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We're looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!
Primary Purpose
The Associate Director, Biostatistics provides leadership and subject matter expertise for the statistical design, analysis, and interpretation of clinical trial data. This role works closely with cross functional teams including clinical operations, data management, medical writing, and regulatory affairs to ensure the integrity, accuracy, and scientific rigor of statistical analyses across multiple studies and therapeutic areas. The Associate Director contributes to the strategic planning of study design and provides guidance on statistical methodology, data analysis, and reporting to support clinical development programs.
Responsibilities
  • Lead and oversee the statistical analysis plan SAP development, study design, and protocol development in collaboration with cross functional teams.
  • Supervise and mentor biostatisticians, providing technical guidance, training, and performance management.
  • Provide statistical input for study protocols, case report form CRF design, and data collection strategies.
  • Ensure high quality statistical deliverables, including tables, listings, figures, and clinical study reports.
  • Conduct complex statistical analyses using appropriate methodologies for clinical trials.
  • Review and approve statistical outputs, results, and programming code generated by team members.
  • Collaborate with medical writing, regulatory, and clinical teams to ensure accuracy and clarity of statistical content in submissions.
  • Support regulatory submissions and respond to queries from health authorities regarding statistical analyses.
  • Provide strategic input for study design, sample size calculations, and adaptive trial methodologies.
  • Drive process improvements and implementation of best practices in biostatistics.
  • Participate in department and corporate initiatives, including SOP development, quality assurance, and methodological advancements.
  • Performs other duties as assigned.
  • Complies with all policies and standards.

Qualifications
  • Master's Degree in Biostatistics, Statistics or a related scientific discipline or PhD in Biostatistics, Statistics, Mathematics, Epidemiology, or a related scientific discipline.
  • 7-9 years experience in biostatistics within the pharmaceutical, biotechnology, or clinical research environment.
  • 4-6 years Proven experience in clinical trial design, statistical programming, and data analysis.
  • 4-6 years Experience supervising or leading a team of biostatisticians.
  • 4-6 years Strong knowledge of statistical software such as SAS, R, or Python
  • 4-6 years Familiarity with regulatory requirements and guidance from FDA, EMA, or other health authorities.
  • 4-6 years Experience with global clinical trials and multi-center studies.

Why work at Emmes?
At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including:
  • Flexible Approved Time Off

  • Tuition Reimbursement

  • 401k Retirement Plan
  • Work From Home Anywhere in the US

  • Maternal/Paternal Leave

  • Casual Dress Code & Work Environment

CONNECT WITH US!
Follow us on Twitter - @EmmesCRO
Find us on LinkedIn - Emmes
The Emmes Company, LLC is an equal opportunity employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability or protected veteran status.
#LI-Remote

Apply