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Clinical Statistician Jobs in Raleigh, NC (NOW HIRING)

Work closely with Quantitative Clinical Pharmacology, Translational Sciences and Statistics to develop protocols and summarize analysis * Contribute to the development of program strategy for ...

Work closely with Quantitative Clinical Pharmacology, Translational Sciences and Statistics to develop protocols and summarize analysis * Contribute to the development of program strategy for ...

Strong experience supporting HIV clinical trials and drug development within the pharmaceutical or biotechnology industry. * Advanced degree in Statistics, Computer Science, Data Science, or a ...

Statistical Scientist

Durham, NC · On-site +1

$96K - $241K/yr

Experience in Early Clinical Development phases with Pharmacokinetic/Pharmacodynamic endpoints ... statistics From camaraderie to professional development, working at IQVIA provides unique ...

Statistical Scientist

Durham, NC · On-site

$96K - $241K/yr

Experience in Early Clinical Development phases with Pharmacokinetic/Pharmacodynamic endpoints ... statistics From camaraderie to professional development, working at IQVIA provides unique ...

Works collaboratively with Clinical Development staff to meet project deliverables and timelines for statistical data analysis and reporting. * Generates or oversees the production of programming ...

Works collaboratively with Clinical Development staff to meet project deliverables and timelines for statistical data analysis and reporting. * Generates or oversees the production of programming ...

Showing results 21-40

Clinical Statistician information

See Raleigh, NC salary details

$49.1K

$84.5K

$113.2K

How much do clinical statistician jobs pay per year?

As of Sep 6, 2026, the average yearly pay for clinical statistician in Raleigh, NC is $84,490.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,900.00 and $95,700.00 per year, depending on experience, location, and employer.

What is a clinical statistician?

Clinical statisticians are professionals who apply statistical methods to the design, analysis, and interpretation of data from clinical trials and medical research. They work closely with physicians, researchers, and regulatory agencies to ensure that clinical studies are scientifically valid and meet regulatory requirements. Their work is crucial in determining the safety and effectiveness of new drugs, treatments, and medical devices. Clinical statisticians often contribute to study design, data management, and the communication of results through reports and publications.

How does a clinical statistician typically collaborate with clinical research teams during a study?

Clinical Statisticians work closely with clinical research teams by designing statistical analysis plans, advising on study protocols, and ensuring data quality and integrity throughout the trial. They frequently attend project meetings, interpret data trends, and communicate findings to medical professionals, regulatory staff, and data managers. This collaborative environment ensures that statistical insights are clearly understood and integrated into decision-making, making strong communication and teamwork skills essential in this role.

What are the key skills and qualifications needed to thrive as a clinical statistician, and why are they important?

To thrive as a Clinical Statistician, you need strong statistical analysis skills, a solid background in mathematics or biostatistics, and at least a bachelor's or master's degree in a related field. Familiarity with statistical software such as SAS, R, or SPSS, as well as knowledge of clinical trial protocols and regulatory guidelines, is essential. Excellent problem-solving abilities, teamwork, and clear communication are standout soft skills for collaborating with clinical teams and presenting complex data. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and the successful interpretation of clinical trial outcomes.

What is the difference between Clinical Statistician vs Biostatistician?

AspectClinical StatisticianBiostatistician
Required CredentialsMaster's or PhD in Statistics, Biostatistics, or related fieldMaster's or PhD in Biostatistics, Statistics, or related field
Work EnvironmentPharmaceutical companies, clinical research organizations, healthcare settingsPublic health agencies, research institutions, healthcare organizations
Industry UsagePrimarily in clinical trials and drug developmentBroader public health research, epidemiology, and clinical studies

While both Clinical Statisticians and Biostatisticians analyze health data and require similar educational backgrounds, Clinical Statisticians mainly focus on clinical trials and drug development within pharmaceutical settings. Biostatisticians have a broader scope, including public health and epidemiology research. The roles often overlap, but the specific industry focus distinguishes them.

What are popular job titles related to Clinical Statistician jobs in Raleigh, NC?

For Clinical Statistician jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Statistician jobs in Raleigh, NC look for?

The top searched job categories for Clinical Statistician jobs in Raleigh, NC are:

Infographic showing various Clinical Statistician job openings in Raleigh, NC as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $84,490 per year, or $40.6 per hour.

Principal Statistical Programmer

PharPoint Research, Inc

Durham, NC • On-site

Full-time

Re-posted 20 days ago


Job description

Job Type
Full-time
Description
BASIC SUMMARY:
Provide overall technical, administrative and functional oversight for the programming activities supporting biostatistics which include the development of analysis datasets, and statistical summaries. Oversee the efficient, accurate, and timely execution of all programming activities within biostatistics. Ensure compliance of the programming group in accordance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs) set forth by PharPoint Research, Inc. and its sponsor clients.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
  • Efficiently and effectively coordinate statistical programming activities for at least 4 projects simultaneously which could be satisfied by 4 separate protocols, a program consisting of at least 2 separate compounds with multiple studies per compound, or NDA submission.
  • Plan and coordinate processes to ensure quality and efficient programming, verification, and documentation of programs for use in creating clinical databases, analysis datasets, tables, listings, and figures.
  • Provide senior level oversight for departmental teams.
  • Ensure the efficiency, quality, and integrity of analyses, data reporting, project, and supervisory activities executed.
  • Successfully represent the department and the company in client meetings/presentations and maintain a positive working relationship with sponsors, regulatory agencies, collaborating associates, vendor personnel and subcontract personnel.
  • Facilitate advanced technical expertise, in conjunction with internal and external team members, to design, implement, validate, and maintain project reporting applications that are supported by the department.
  • Identify project priorities and project timeline goals and communicate priority-related issues and timelines to programming teams.
  • Recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
  • Efficiently manage project budgets to identify resourcing or scope of work changes.
  • Provide accurate and timely project status updates to other team members, colleagues, and senior management.
  • Serve as a model to departmental subordinates as it relates to effective time management, communication, and utilization of resources. Provide leadership and motivation to departmental personnel.
  • Contribute to ongoing improvement of programming processes and methodology.
  • Provide senior leadership and guidance to departmental employees to ensure accuracy and adherence to pertinent departmental policies, practices, and procedures.
  • Manage activities of assigned project team(s) to ensure effective performance of a clinical trial program. Provide direction to team members working toward a common goal and successfully coordinate multiple priorities.
  • Interact collaboratively with staff across departments to ensure that project and departmental activities are successfully completed.
  • May participate in the interview and selection of qualified personnel.
  • Assist in the development, implementation, and delivery of departmental training programs; server as a mentor to junior level programmers.
  • May attend related continuing education programs, professional meetings, and/or company career development activities sponsored or approved by the company.
  • Assist in the development, maintenance, and communication of departmental systems and SOPs.
  • Perform all other related duties as assigned.

Requirements
QUALIFICATIONS:
  • Education: Bachelor's degree (B.A./B.S.) or equivalent in Statistics, Computer Science or related field.
  • Experience: 9 years relevant experience in clinical research. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • Certification/Licensure: None
  • Other: Effective team player: willingness to go the extra distance to get results, meet deadlines, etc. Able to manage many projects simultaneously, to manage conflicting priorities, and to be flexible when priorities change. Strong ability to motivate staff within project teams and ensure productivity and smooth operation in conditions with ambiguity. Leadership skills in priority evaluations, adapting to changes, conflicts resolutions, and effective partnership. Knowledge of one or more statistical software packages used to conduct statistical analyses required. Ability to read, write, speak, and understand English required.

PHYSICAL DEMANDS:
  • While performing the duties of this job, the employee is regularly required to talk, hear, and type at a computer.
  • Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:
  • General office working conditions, the noise level in the work environment is usually quiet.

COMMENTS:
  • This position may require occasional domestic/international travel.
  • Must have a valid driver's license with no limitations on driving availability.