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Weekend Statistical Programmer Jobs in Raleigh, NC

UCB

Statistical Methodologist, Raleigh, NC

Raleigh, NC · On-site

Experience with R, SAS, or similar statistical programming languages * Ability to explain complex statistical concepts to non-statistical audiences * Strong written and verbal communication skills in ...

UCB

Statistical Methodologist, Raleigh, NC

Raleigh, NC · Hybrid

Proficiency in statistical programming, including R and/or SAS. * Knowledge of global regulatory frameworks, including FDA and EMA guidance. * Ability to communicate complex statistics to technical ...

Fortrea

Senior Programmer Analyst- Remote, US

Durham, NC · On-site

$90K - $120K/yr

Serve as Lead Statistical Programmer providing programming support for development and maintenance of SDTM/Client standards datasets. * Develop/validate Custom/Complex SDTM domains and efficiently ...

GILERO

Manufacturing Engineer

Pittsboro, NC · On-site

$50K - $65K/yr

Characterize and optimize processes using statistical techniques, engineering knowledge and ... Must be willing to work shifts, additional hours and weekend/ holidays as required by business ...

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All JobsStatistical Programmer JobsWeekend Statistical Programmer JobsWeekend Statistical Programmer Jobs in Raleigh, NC

Weekend Statistical Programmer information

See Raleigh, NC salary details

$82.1K

$143.2K

$242K

How much do weekend statistical programmer jobs pay per year?

As of Sep 1, 2026, the average yearly pay for weekend statistical programmer in Raleigh, NC is $143,179.00, according to ZipRecruiter salary data. Most workers in this role earn between $121,500.00 and $155,500.00 per year, depending on experience, location, and employer.

What is the difference between Weekend Statistical Programmer vs Full-Time Statistical Programmer?

AspectWeekend Statistical ProgrammerFull-Time Statistical Programmer
CredentialsBachelor's degree in Biostatistics, Statistics, or related field; often requires programming certificationsSame as weekend role, with additional experience preferred
Work EnvironmentPart-time, flexible hours, often remote or in clinical research settingsFull-time, standard office or remote work in pharmaceutical or biotech companies
Employer & Industry UsageUsed in clinical trials, research organizations, and CROs for flexible staffingCommon in pharmaceutical, biotech, and research institutions for ongoing project support

The main difference between a Weekend Statistical Programmer and a Full-Time Statistical Programmer lies in their work hours and commitment. Weekend roles typically involve part-time, flexible schedules focused on specific project needs, while full-time roles require consistent, ongoing work. Both roles require similar skills and credentials, but the work environment and hours differ to accommodate project demands and work-life balance.

What are the most commonly searched types of Statistical Programmer jobs in Raleigh, NC?

The most popular types of Statistical Programmer jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Weekend Statistical Programmer jobs?

Cities near Raleigh, NC with the most Weekend Statistical Programmer job openings:

Weekend Statistical Programmer jobs near you

FSP Principal Biostatistician, Study Powering and Design

Durham, NC • On-site

IQVIA, Inc.
Health Care and Social Assistance • 10K+ employees

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

63rd of 226 rated it services

People enjoy working here

Good employer

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Learn more about IQVIA, Inc.external

$115K - $243K/yr

Full-time

Re-posted 11 days ago

Job description

Job Level: FSP Principal Biostatistician, Study Powering and Design
Location: Home-based in the U.S. or Canada
Why DSSS?
Data Sciences Staffing Solutions, DSSS, is a unit within IQVIA that provides our sponsors with fully embedded resources through a Functional Service Provider (FSP) partnership. This yields all the benefits of working for an industry leading global CRO and collaborating directly with cross-functional sponsor teams. Sponsor clients include world class pharmaceutical and biotech companies offering you unique opportunities to influence the future of medicine and advance therapies to market.
Job Summary:
The Principal Biostatistician is responsible for providing statistical support for pharmaceutical clinical trials in patients.
Additional Benefits:
  • Home-based remote working opportunities.
  • Work/life balance as well as flexible schedules.
  • Collaborating with motivated, high-performance, statistical and research teams.
  • Technical training and tailored development curriculum.
  • Research opportunities that match your unique skillset.
  • Promising career trajectory.
  • Job stability: long-term engagements and re-deployment opportunities.
  • Focus on bringing new therapies to market rather than project budgets and change orders.
  • Experience with regulatory submissions.
  • Engaging, fast-paced environment.
  • Good work-life balance.

Job Responsibilities:
  • Collaborate with multi-disciplinary project teams to establish project objectives and timelines.
  • Perform samples size and power calculations for optimizing study design
  • Author statistical analysis plans.
  • Collaborate with Data Management, Clinical Development, and Clinical Operations with statistical expertise.
  • Author or review analysis dataset and TLF specifications
  • Validation programming of efficacy analysis datasets plus tables, listings, and figures (TLF)
  • Provide guidance and supervision to programmers in authoring analysis dataset specifications and programming/validation of tables, listings, and figures for safety, etc.
  • Interpret study results and review reports of study results for accuracy.
  • Support exploratory analyses.
  • Participate in IND or NDA activities.
  • Monitor internal and CRO project activities including timelines, deliverables, and availability of resources.
  • Contribute to clinical study reports and other regulatory documents, e.g. NDA, DSURs, Briefing Documents, ISS, ISE, SCE (Summary of Clinical Efficacy), SCS (Summary of clinical Safety).

Qualifications (Required)
  • PhD in Statistics, Biostatistics, or related field with 3+ years of industry experience.
  • MS in Statistics, Biostatistics, or related field with 5+ years of industry experience.
  • At least 2 years in Phase 2/3 clinical trial experience.
  • At least 3 years of experience in supporting simulations, sample size and power calculations
  • Demonstrated ability to work pro-actively and independently.
  • Able to effectively communicate statistical ideas and collaborate with cross-functional teams
  • Ability to efficiently use R or SAS to perform analyses.
  • Support of various regulatory submissions
  • Understanding of relevant FDA guidance, ICH GCP, ICH E9 plus general knowledge of industry practices and standards.
  • Experience in validation/programming of ADAM and TLF
  • Experience with CDISC, including SDTM, ADAM, CDASH
  • Solid understanding of estimands and multiple imputation methods.

Desired Experience:
  • Supporting written communications with regulators.
  • 1+ years of experience with immunology therapeutic area.
  • Bayesian methods

#LI-Remote
#LI-NITINMAHAJAN
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $115,900.00 - $243,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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