... statistical summaries. Oversee the efficient, accurate, and timely execution of all programming ... Ensure compliance of the programming group in accordance with Good Clinical Practice (GCP) and ...
... statistical summaries. Oversee the efficient, accurate, and timely execution of all programming ... Ensure compliance of the programming group in accordance with Good Clinical Practice (GCP) and ...
... statistical summaries. Oversee the efficient, accurate, and timely execution of all programming ... Ensure compliance of the programming group in accordance with Good Clinical Practice (GCP) and ...
... statistical summaries. Oversee the efficient, accurate, and timely execution of all programming ... Ensure compliance of the programming group in accordance with Good Clinical Practice (GCP) and ...
... statistical summaries. Oversee the efficient, accurate, and timely execution of all programming ... Ensure compliance of the programming group in accordance with Good Clinical Practice (GCP) and ...
Quick apply
... statistical summaries. Oversee the efficient, accurate, and timely execution of all programming ... Ensure compliance of the programming group in accordance with Good Clinical Practice (GCP) and ...
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 ...
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 ...
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 ...
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 ...
Senior Clinical Scientist
Raleigh, NC · On-site
Work closely with Quantitative Clinical Pharmacology, Translational Sciences and Statistics to develop protocols and summarize analysis * Contribute to the development of program strategy for ...
Senior Clinical Scientist
Raleigh, NC · On-site
Work closely with Quantitative Clinical Pharmacology, Translational Sciences and Statistics to develop protocols and summarize analysis * Contribute to the development of program strategy for ...
Principal Statistical Programmer
Durham, NC · On-site
$140 - $180/hr
The Senior Medical Director, in partnership with the Principal Statistical Programmer, will play a pivotal role in advancing our mission to leave no patient behind by ensuring clinical excellence in ...
Principal Statistical Programmer
Durham, NC · On-site
$140 - $180/hr
The Senior Medical Director, in partnership with the Principal Statistical Programmer, will play a pivotal role in advancing our mission to leave no patient behind by ensuring clinical excellence in ...
Who you will work with You will be working in a team that provides statistical consultancy across therapy areas and development stages, partnering closely with colleagues in clinical development ...
Who you will work with You will be working in a team that provides statistical consultancy across therapy areas and development stages, partnering closely with colleagues in clinical development ...
Who you will work with You will be working in a team that provides statistical consultancy across therapy areas and development stages, partnering closely with colleagues in clinical development ...
Who you will work with You will be working in a team that provides statistical consultancy across therapy areas and development stages, partnering closely with colleagues in clinical development ...
Work closely with Quantitative Clinical Pharmacology, Translational Sciences and Statistics to develop protocols and summarize analysis * Contribute to the development of program strategy for ...
Quick apply
Work closely with Quantitative Clinical Pharmacology, Translational Sciences and Statistics to develop protocols and summarize analysis * Contribute to the development of program strategy for ...
Senior Clinical Scientist
Raleigh, NC · On-site +1
Work closely with Quantitative Clinical Pharmacology, Translational Sciences and Statistics to develop protocols and summarize analysis * Contribute to the development of program strategy for ...
Senior Clinical Scientist
Raleigh, NC · On-site +1
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 ...
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 ...
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 ...
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 ...
Overview Maintains expert knowledge of clinical performance data and advanced statistical and analytic knowledge to convert data into actionable clinical insight. Provides data analysis in an ...
Overview Maintains expert knowledge of clinical performance data and advanced statistical and analytic knowledge to convert data into actionable clinical insight. Provides data analysis in an ...
Principal Statistical Programmer
Durham, NC · On-site
$130 - $180/hr
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 ...
New
Principal Statistical Programmer
Durham, NC · On-site
$130 - $180/hr
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 ...
New
Sr Statistical Programmer (NA Only)
Morrisville, NC · On-site
$80.60 - $145/hr
Develop specifications for datasets and outputs of any complexity according to statistical and ... Extensive programming experience in SAS or other required software, preferably in a clinical trial ...
Sr Statistical Programmer (NA Only)
Morrisville, NC · On-site
$80.60 - $145/hr
Develop specifications for datasets and outputs of any complexity according to statistical and ... Extensive programming experience in SAS or other required software, preferably in a clinical trial ...
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 +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 ...
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 ...
Senior Manager, Statistical Programming
Raleigh, NC · On-site
$169K - $219K/yr
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 ...
Senior Manager, Statistical Programming
Raleigh, NC · On-site
$169K - $219K/yr
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 ...
Senior Manager, Statistical Programming
Raleigh, NC · On-site
$169K - $219K/yr
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 ...
Senior Manager, Statistical Programming
Raleigh, NC · On-site
$169K - $219K/yr
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 ...
Clinical Statistician information
See Raleigh, NC salary details
$49.1K - $54.9K
5% of jobs
$59.1K is the 25th percentile. Wages below this are outliers.
$54.9K - $60.8K
27% of jobs
$60.8K - $66.6K
1% of jobs
$66.6K - $72.4K
6% of jobs
$72.4K - $78.2K
1% of jobs
$78.2K - $84.1K
0% of jobs
$84.1K - $89.9K
0% of jobs
The median wage is $92.8K / yr.
$89.9K - $95.7K
18% of jobs
$99.6K is the 75th percentile. Wages above this are outliers.
$95.7K - $101.6K
24% of jobs
$101.6K - $107.4K
0% of jobs
$107.4K - $113.2K
17% of jobs
$49.1K
$84.5K
$113.2K
How much do clinical statistician jobs pay per year?
What is a clinical statistician?
How does a clinical statistician typically collaborate with clinical research teams during a study?
What are the key skills and qualifications needed to thrive as a clinical statistician, and why are they important?
What is the difference between Clinical Statistician vs Biostatistician?
| Aspect | Clinical Statistician | Biostatistician |
|---|---|---|
| Required Credentials | Master's or PhD in Statistics, Biostatistics, or related field | Master's or PhD in Biostatistics, Statistics, or related field |
| Work Environment | Pharmaceutical companies, clinical research organizations, healthcare settings | Public health agencies, research institutions, healthcare organizations |
| Industry Usage | Primarily in clinical trials and drug development | Broader 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.
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Full-time
Re-posted 20 days ago
Job description
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.
About PharPoint Research
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
51 - 200 Employees
Headquarters location
Durham, NC, US
Year founded
2007