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Manager Statistical Programming Jobs in Frederick, MD

Emmes

Senior Biostatistician

Rockville, MD · On-site +1

Manages statistical activities for a clinical study or platform of clinical studies ... May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and ...

VENESCO, LLC

SAS Programmer

Fort Detrick, MD · On-site

$135K - $148K/yr

Collaborate with Clinical Data Management and Biostatistics teams. * Maintain programming documentation and standards. Minimum Qualifications * Bachelor's degree in Statistics, Computer Science ...

VENESCO LLC

SAS Programmer

Frederick, MD · On-site

$135K - $148K/yr

Collaborate with Clinical Data Management and Biostatistics teams. * Maintain programming documentation and standards. Minimum Qualifications * Bachelor's degree in Statistics, Computer Science ...

BullFrog AI

Staff AI Engineer

Gaithersburg, MD · On-site

... management. Responsibilities : • Advance the core algorithms by improving ranking quality ... Computer-science-with-statistics or statistics-with-computer-science backgrounds are welcome. • ...

VB Spine

Sr. Quality Engineer

Leesburg, VA · On-site

$100K - $110K/yr

Apply statistical tools and process control methods to support quality system processes and management reviews * Collaborate with Regulatory on Instructions for Use (IFUs) and review/approve quality ...

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

Manager Statistical Programming information

See Frederick, MD salary details

$84K

$146.4K

$247.6K

How much do manager statistical programming jobs pay per year?

As of Aug 16, 2026, the average yearly pay for manager statistical programming in Frederick, MD is $146,448.00, according to ZipRecruiter salary data. Most workers in this role earn between $124,300.00 and $159,100.00 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 Frederick, MD?

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

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

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

Manager Statistical Programming jobs near you
Infographic showing various Manager Statistical Programming job openings in Frederick, MD as of August 2026, with employment types broken down into 100% Full Time. Highlights an 72% In-person, and 28% Remote job distribution, with an average salary of $146,448 per year, or $70.4 per hour.

Senior Biostatistician

Emmes

Rockville, MD • On-site, Remote

Full-time

Medical, Retirement

Re-posted 10 days ago

Job description

Overview

Senior Biostatistician

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

Leads collaborations with clinical investigators to determine study design, contributes to protocol development, authors statistical analysis plans, performs statistical analysis, makes statistical inference and writes and presents reports summarizing findings including publications in peer reviewed journals. Manages statistical activities for a clinical study or platform of clinical studies.

Responsibilities
  • Provides sound strategic, scientific and statistical input to support client's research projects.
  • Serves as the lead Biostatistician on one or more study projects.
  • May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies.
  • Leads the project team's development of study analysis plans and statistical programs to perform analyses and display study data.
  • Keeps abreast with current statistical and medical literature to ensure that sound methodologies are adopted.
  • Fosters innovation in Biostatistics that will continuously enhance current statistical knowledge and practices.
  • Ensures the scientific integrity of the research project and the accuracy of the reported results.
  • Performs sample size calculation and provides leadership in the statistical design of research projects.
  • Reviews protocols and case report forms to ensure that protocol objectives are met, and standards are maintained.
  • Develops study assignment allocation schemas along with appropriate documentation.
  • Leads the development of the methods and results sections of clinical study reports and scientific publications.
  • Represents EMMES on behalf of clients at regulatory meetings.
  • Participate in the development and updating of Standard Operating Procedures.
  • Performs other duties as assigned
  • Complies with all policies and standards
Qualifications
  • PhD Biostatistics, statistics, epidemiology or related field required
  • 4-6 years of related experience is expected but not required for the position.
  • 1-3 years Demonstrated proficiency with statistical methods and applications in clinical research required.
  • 1-3 years Strong programming skills in SAS and/or R required.

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 

Employment Type: FULL_TIME
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About Emmes

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

201 - 500 Employees

Headquarters location

Rockville, MD, US

Year founded

1977

Social media

Twitter

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