ZipRecruiter

Log In

1

Senior Manager Statistical Programming Jobs in Raleigh, NC

TIBCO

Senior Manager, Software Engineering

Raleigh, NC · On-site

The Senior Manager of Security will play a pivotal role in ensuring the security, compliance, and ... Cloud Security Engineering: Oversee the design, implementation, and maintenance of effective ...

Actalent

Senior Manager, Project Engineer

Oxford, NC · On-site

Job Title: Sr. Manager, Project Engineer The Sr. Project Engineering Manager leads capital equipment, automation, packaging, and manufacturing improvement projects that support high-volume production ...

previous page

Showing results 41-60

All JobsStatistical Programming JobsSenior Manager Statistical Programming JobsSenior Manager Statistical Programming Jobs in Raleigh, NC

Senior Manager Statistical Programming information

See Raleigh, NC salary details

$23.3K

$96.2K

$162.3K

How much do senior manager statistical programming jobs pay per year?

As of Sep 10, 2026, the average yearly pay for senior manager statistical programming in Raleigh, NC is $96,244.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,600.00 and $104,000.00 per year, depending on experience, location, and employer.

How does a senior manager statistical programming typically collaborate with cross-functional teams in clinical research projects?

A Senior Manager Statistical Programming plays a pivotal role in coordinating with biostatisticians, clinical data managers, and medical writers to ensure seamless data flow and analysis throughout clinical trials. They oversee programming teams to deliver statistical outputs, such as tables, listings, and figures, while maintaining compliance with regulatory standards. Regular meetings and clear communication are essential, as the Senior Manager must interpret project requirements and translate them into actionable programming tasks, ensuring timelines and quality standards are met. This collaborative environment fosters continuous learning and problem-solving, as cross-functional input is vital for addressing complex data challenges.

What are the key skills and qualifications needed to thrive as a senior manager statistical programming, and why are they important?

To thrive as a Senior Manager Statistical Programming, you need expertise in biostatistics, programming languages like SAS or R, and experience with clinical trial data, typically supported by an advanced degree in a quantitative field. Familiarity with regulatory requirements (e.g., CDISC standards), clinical data management systems, and project management tools is essential. Strong leadership, communication, and problem-solving skills help you lead teams and liaise with cross-functional stakeholders. These skills ensure accurate, compliant data analyses and effective team management for successful clinical trial outcomes.

What is the difference between Senior Manager Statistical Programming vs Statistical Programmer?

AspectSenior Manager Statistical ProgrammingStatistical Programmer
CredentialsBachelor's/Master's in Biostatistics, Computer Science, or related field; often with management experienceBachelor's or Master's in Biostatistics, Statistics, or related field
Work EnvironmentLeads teams, manages projects, collaborates with cross-functional teamsPerforms data analysis, programming, and validation tasks under supervision
Employer & Industry UsagePharmaceutical, biotech companies, CROs, clinical researchPharmaceutical, biotech, clinical research organizations

The main difference is that Senior Manager Statistical Programming oversees teams and manages projects, while Statistical Programmers focus on executing data analysis and programming tasks. The senior role involves leadership responsibilities, whereas the programmer role is more technical and task-oriented.

What are popular job titles related to Senior Manager Statistical Programming jobs in Raleigh, NC?

For Senior Manager Statistical Programming jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Senior Manager Statistical Programming jobs in Raleigh, NC look for?

The top searched job categories for Senior Manager Statistical Programming jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Senior Manager Statistical Programming jobs?

Cities near Raleigh, NC with the most Senior Manager Statistical Programming job openings:

Senior Manager Statistical Programming jobs near you
Infographic showing various Senior Manager Statistical Programming job openings in Raleigh, NC as of September 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $96,244 per year, or $46.3 per hour.

Senior Statistician

Durham, NC • On-site, Remote

Worldwide Clinical Trials
Scientific Research and Development Services • 10K+ employees
Learn more about Worldwide Clinical Trialsexternal

$84K - $103K/yr

Full-time

Re-posted 6 hours ago

Key responsibilities

  • Manage statistical support for one or more projects, providing expert and timely consultancy.

  • Review study designs, analysis plans, reports, and assist in the design of clinical trials including statistical sections and analysis plans.

  • Develop, evaluate, and run SAS programs for data analysis and reporting, including validation and documentation.

Job description

Who we are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What the Senior Statistician does at Worldwide
Independently manages statistical project support and provides expert statistical consultancy across the stats function.
What you will do
  • Manage the statistics support to one or more projects/sponsor programs of work, ensuring that needs are met by expert and timely statistical consultancy and support
  • Provides expert review of study designs, analysis plans, and reports
  • Assist sponsors in the design of clinical trials, including statistical sections of the study protocol, randomization methodology, and writing statistical analysis plans
  • Consult with internal departments, sponsors, and other third parties regarding statistical issues and reporting requirements
  • Provide project support to the statistics reporting process through the specification/review of tables, figures, and listings shells, writing/review of derived dataset specifications, and the formatting of report documents and tabulations
  • Undertake the preparation of final reports, including the production of tables, listings, and figures, and report writing
  • Develop, evaluate, and run Statistical Analysis System (SAS) programs for the statistical analysis and reporting of clinical study data. This includes programs for derived datasets, Clinical Data Interchange Standards Consortium (CDISC), Study Data Tabulation Model (SDTM), and Analysis Data Model (ADaM) datasets, tables, figures, and listings, and their validation
  • Ensure the maintenance of documentation, e.g., the description of programs and validation
  • Produce ad hoc data summaries when requested during a trial.
    Extract information from the system during a trial, e.g., summaries, data listings, study data sets.
  • Validate software, in the role of system owner or tester, and test SAS Macros, maintaining the required validation and testing documentation
  • Make statistical contributions to manuscripts for publication/presentation
  • Provide support for the bidding process, including contribution to budget review, proposals, and bid defense meetings
  • Lead the identification of system and process improvements, and develop and implement solutions to improve the efficiency and quality of clinical study data processing and reporting
  • Support the development of statistical design and analysis policies
  • Maintain knowledge in design consultancy and analysis methodology, statistical software packages (e.g., SAS and nQuery), and regulatory guidance documents, e.g. International Council for Harmonization (ICH), Food and Drug Administration (FDA), and Committee for Medicinal Products (CPMP) points to consider
  • Assist with Quality Assurance and Audit requirements
  • Assist the Director of Biostatistics with all other aspects of the job as required
  • Perform all activities in compliance with Worldwide Clinical Trials and agreed sponsor quality system standards, relevant ICH standards, and specifically with FDA Quality System Regulation (including 21CFR Part 11)
  • Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

What you bring to the role:
  • Computer literate and numerate with a proven ability to adapt to various computer systems
  • Expert-level project statistician experienced in providing statistical leadership to projects
  • Design and analysis consultancy skills and knowledge across a broad range of applications, together with key competencies in customer focus, delivering on commitments, building strong relationships, communicating, influencing, and embracing innovation and change

Your experience
  • Master's level in mathematics, statistics, or another subject required with a strong statistical component
  • Minimum 3 years of statistical experience leading clinical trial projects and data analysis

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $87,500.00 - $173,500.00
The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Apply