1

Associate Statistical Programmer Jobs in Clayton, NC

Perform in-depth data analysis using advanced statistical and bioinformatics tools, and draw ... Collaborate effectively with research scientists, engineers, and other team members to achieve ...

Perform in-depth data analysis using advanced statistical and bioinformatics tools, and draw ... Collaborate effectively with research scientists, engineers, and other team members to achieve ...

... apply statistical tools to evaluate process performance, including but not limited to process ... Mentor junior validation associates in Process Validation, cGMP regulations, and principles of ...

... apply statistical tools to evaluate process performance, including but not limited to process ... Mentor junior validation associates in Process Validation, cGMP regulations, and principles of ...

Staying on top of market statistics and trends * Consult and advise clients on their real estate ... Manage progression of escrow process working with photographers, engineers, environmental surveyors ...

New

... Associate, you will play a pivotal role in designing and implementing seamless integration ... Engineering, Mathematics/Statistics, Operations/Supply Chain - Demonstrating proficiency in Agile ...

Engineer 3, DPFG MSAT

Holly Springs, NC

$63K - $81K/yr

Contributes to the management of manufacturing data (i.e., databasing) and the statistical analysis ... Associate's degree in Engineering, Life Science or Chemical Engineering with 7 years of applicable ...

Engineer 3, DPFG MSAT

Holly Springs, NC · On-site

$63K - $81K/yr

Contributes to the management of manufacturing data (i.e., databasing) and the statistical analysis ... Associate's degree in Engineering, Life Science or Chemical Engineering with 7 years of applicable ...

Engineer 3, DPFG MSAT

Holly Springs, NC

$63K - $81K/yr

Contributes to the management of manufacturing data (i.e., databasing) and the statistical analysis ... Associate's degree in Engineering, Life Science or Chemical Engineering with 7 years of applicable ...

Sr. Controls Engineer

Middlesex, NC · On-site

$97K - $143K/yr

Support and provide production associates with the tools required to perform the job in a manner to ... Required Basic Qualifications: • Bachelor degree in an Engineering discipline from an accredited ...

Principal Data Scientist

Raleigh, NC · On-site +1

$147K - $243K/yr

... including Python; feature engineering using statistical techniques; data querying and ... Spread across 40+ countries, our associates work flexibly across work environments, from in-office ...

CAD TECHNICIAN II

Raleigh, NC · On-site

$45K - $60K/yr

Reasonable ability to perform mathematical and statistical computations. * Intermediate knowledge ... Possess an associate degree in Engineering, Architecture, Planning, Surveying, or a closely related ...

CAD TECHNICIAN II

Raleigh, NC · On-site

$45K - $60K/yr

Reasonable ability to perform mathematical and statistical computations. * Intermediate knowledge ... Possess an associate degree in Engineering, Architecture, Planning, Surveying, or a closely related ...

Showing results 41-60

Associate Statistical Programmer information

See Clayton, NC salary details

$71.9K

$125.3K

$211.8K

How much do associate statistical programmer jobs pay per year?

As of Aug 12, 2026, the average yearly pay for associate statistical programmer in Clayton, NC is $125,277.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,300.00 and $136,100.00 per year, depending on experience, location, and employer.

What is an associate statistical programmer?

An Associate Statistical Programmer is an entry-level professional who assists in the programming and analysis of clinical trial data, primarily within the pharmaceutical or biotechnology industries. They use statistical software, such as SAS or R, to create, validate, and maintain datasets, tables, listings, and figures required for clinical study reports. Their work supports biostatisticians and clinical teams in ensuring data accuracy and regulatory compliance. This role is ideal for those with a background in statistics, mathematics, or computer science, looking to start a career in clinical data analysis.

How does an associate statistical programmer typically collaborate with biostatisticians and data managers in clinical research projects?

As an Associate Statistical Programmer, you will frequently collaborate with biostatisticians to understand statistical analysis plans and translate them into clear programming specifications. You’ll also work closely with data managers to ensure data integrity and resolve any data discrepancies before analysis. Effective communication and teamwork are essential, as you’ll often participate in project meetings, provide programming support, and help deliver high-quality datasets and reports under tight timelines. This collaborative environment is key to ensuring accurate and timely clinical trial results.

What is the difference between Associate Statistical Programmer vs Statistical Programmer?

AspectAssociate Statistical ProgrammerStatistical Programmer
Required CredentialsBachelor's degree in statistics, mathematics, or related field; some roles may require basic programming skillsBachelor's or master's degree; more experience in programming and statistical analysis
Work EnvironmentEntry-level, supporting senior programmers; often in clinical research or pharmaceutical companiesMore independent, handling complex analyses; similar industry settings
Employer & Industry UsageCommon in clinical trials, pharmaceutical, and biotech companiesUsed across similar industries, often as a step up from associate roles

The main difference between an Associate Statistical Programmer and a Statistical Programmer lies in experience and responsibility level. Associate roles are typically entry-level, focusing on supporting tasks under supervision, while Statistical Programmers handle more complex analyses independently. Both roles are vital in clinical research and biotech industries, with the associate position serving as a stepping stone to more advanced programming roles.

What are the key skills and qualifications needed to thrive as an associate statistical programmer, and why are they important?

To thrive as an Associate Statistical Programmer, you need a solid background in statistics, programming (especially SAS or R), and familiarity with clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Proficiency with statistical software (such as SAS, R, or Python), CDISC standards, and data management tools is essential, and certifications in SAS programming can be advantageous. Attention to detail, strong problem-solving abilities, and effective communication skills help you collaborate with clinical teams and ensure data quality. These skills and qualities are vital for delivering accurate statistical analyses that support regulatory submissions and evidence-based decision-making in clinical research.
What are the most commonly searched types of Statistical Programmer jobs in Clayton, NC? The most popular types of Statistical Programmer jobs in Clayton, NC are:
What are popular job titles related to Associate Statistical Programmer jobs in Clayton, NC? For Associate Statistical Programmer jobs in Clayton, NC, the most frequently searched job titles are:
What cities near Clayton, NC are hiring for Associate Statistical Programmer jobs? Cities near Clayton, NC with the most Associate Statistical Programmer job openings:
Infographic showing various Associate Statistical Programmer job openings in Clayton, NC as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $125,277 per year, or $60.2 per hour.

Associate Scientist, Immunology

Asklepios BioPharmaceutical, Inc.

Durham, NC • On-site

Full-time

Posted 11 days ago


Job description

AskBio Inc., a wholly owned and independently operated subsidiary of Bayer AG, is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb-girdle muscular dystrophy, multiple system atrophy, Parkinson's disease, and Pompe disease. AskBio's gene therapy platform includes Pro10, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park, North Carolina, and European headquarters in Edinburgh, Scotland, the company has generated hundreds of proprietary capsids and promoters, several of which have entered pre-clinical and clinical testing.

Our vision: Pioneering science to create transformative molecular medicines.

Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.

Our principles:

  • Advance innovative science by pushing boundaries.

  • Bring transformative therapeutics to patients in need.

  • Provide an environment for employees to reach their fullest potential.

Our values:

  • Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.

  • Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.

  • Embrace Responsibility. We are humbled by the enormity of our mission.We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.

  • Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.

  • Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what's right in every situation. Make clear commitments and follow through.

Position Summary

Seeking a highly motivated and detail-oriented Associate Scientist to join our Bioanalytical Group.

The successful candidate will play a key role in developing and validating binding antibody and neutralizing antibody assays performed on preclinical and clinical samples to support our gene therapy programs. This position requires hands-on experience in immune assay techniques and a basic understanding of gene therapy research. The successful candidate will work closely with cross-functional teams to ensure that assays meet regulatory standards and contribute to the advancement of gene therapy projects. The ideal candidate will have a strong background in binding antibody assays, cell culture, and aseptic techniques. This position offers an opportunity to work in a dynamic, fast-paced environment and contribute to the development of innovative gene therapies for patients in need. Antibody assay development, qualification and validation activities will be performed in compliance with GCLP (Good Clinical Laboratory Practices) laboratories, GLP (Good Laboratory Practices), CLIA (Clinical Laboratory Improvement Act), and national, international, and state regulations.

This position is on site in RTP, NC and reports to an Associate Director, Clinical Immunology.

Job Responsibilities

  • Independently design and execute complex assays related to neutralizing and total antibody development, utilizing strong scientific expertise and knowledge of adeno viral vector and cell-based techniques

  • Optimize and troubleshoot experimental protocols to ensure accuracy, reproducibility, and efficiency. Perform neutralizing and total antibody assay validation to meet FDA and CLIA guidelines

  • Perform clinical sample analysis and prepare comprehensive reports for clinical sites

  • Perform in-depth data analysis using advanced statistical and bioinformatics tools, and draw meaningful conclusions from the results

  • Prepare comprehensive reports, presentations, and manuscripts summarizing research findings for internal and external stakeholders

  • Stay current with the latest advancements in gene therapy research and apply this knowledge to your work

  • Collaborate effectively with research scientists, engineers, and other team members to achieve project goals

  • Develop and implement standard operating procedures (SOPs) for maintaining consistent research quality

  • Assist with the preparation and submission of regulatory filings

  • May supervise and mentor junior research staff

Minimum Requirements

  • Bachelor's degree in Immunology, Biology, Biochemistry, Biotechnology, Virology or related field with 8+ years' relevant work experience; or Master's degree in Immunology, Biology, Biochemistry, Biotechnology, Virology or related field with 4+ years' relevant work experience

  • Prior experience in Pharma or CRO industry

  • Basic lab skills, such as adhering GCLP, biosafety and chemical use guidelines (training provided) and making reagents at desired dilutions or concentrations

  • Demonstrated experience in the performing development and validation of ligand binding and neutralizing antibody assay following GLP compliance

  • Experience with mammalian cell culture and performing analytical assays using MSD platform

  • Knowledge of industry practices for the development, qualification/ validation of immunogenicity assays and FDA guidelines

  • Knowledge of Companion Diagnostics

  • Proficiency with MS Office tools (Word, Excel, and PowerPoint)

  • Self-motivated, organized, and individual capable of working independently as well as an active team contributor

  • Strong oral and written communication skills

  • Excellent interpersonal skills with the ability to interact effectively with teams, internally and externally

Preferred Education, Experience and Skills

  • Experience in performing Western blots and protein purification. and processing/handling primary cells such as PBMCs

AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid jobrelated requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561-6210 or sending us an email at careers@askbio.com.

Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio, through any medium, will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio, no fee or payment of any kind will be paid to the agency.