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Manager Statistical Programming Jobs in Ellicott City, MD

Otsuka

Associate Director, Biostatistics

Rockville, MD · On-site +1

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

Emmes Group

Associate Biostatistician

Rockville, MD · On-site

Supports development of statistical analysis plans, other study plans and statistical programming ... Provides project updates to appropriate project or department management staff. * Keeps abreast of ...

New

Emmes

Associate Biostatistician

Rockville, MD · On-site +1

Supports development of statistical analysis plans, other study plans and statistical programming ... Provides project updates to appropriate project or department management staff. * Keeps abreast of ...

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All JobsStatistical Programming JobsManager Statistical Programming JobsManager Statistical Programming Jobs in Ellicott City, MD

Manager Statistical Programming information

See Ellicott City, MD salary details

$84.2K

$146.8K

$248.1K

How much do manager statistical programming jobs pay per year?

As of Sep 7, 2026, the average yearly pay for manager statistical programming in Ellicott City, MD is $146,754.00, according to ZipRecruiter salary data. Most workers in this role earn between $124,500.00 and $159,400.00 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 popular job titles related to Manager Statistical Programming jobs in Ellicott City, MD?

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

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

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

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

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

Manager Statistical Programming jobs near you
Infographic showing various Manager Statistical Programming job openings in Ellicott City, MD as of June 2026, with employment types broken down into 91% Full Time, 2% Temporary, and 7% Contract. Highlights an 96% In-person, 2% Hybrid, and 2% Remote job distribution, with an average salary of $146,754 per year, or $70.6 per hour.

Associate Director Biostatistics

Emmes Group

Rockville, MD • On-site

Full-time

Medical, Retirement

Posted 25 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.
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