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Clinical Trial Statistician Jobs (NOW HIRING)

ICON

Clinical Trial Manager

Raleigh, NC · On-site +1

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... statistical analysis plans * Participate in or lead set-up and implementation of effective ...

Icon plc

Clinical Trial Manager

Raleigh, NC · On-site

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... statistical analysis plans * Participate in or lead set-up and implementation of effective ...

Icon plc

Clinical Trial Manager

Houston, TX · On-site

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... statistical analysis plans * Participate in or lead set-up and implementation of effective ...

Icon plc

Clinical Trial Manager

Philadelphia, PA · On-site

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... statistical analysis plans * Participate in or lead set-up and implementation of effective ...

Icon plc

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... statistical analysis plans * Participate in or lead set-up and implementation of effective ...

Parexel

Clinical Trial Leader

Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring) * Verifies and ... Maintains oversight during clinical trial conduct including adherence to GCP and all global and ...

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

Lead interdisciplinary core trial teams (e.g., data management, statistics, pharmacokinetics, clinical operations) and facilitate Trial Oversight Meetings. Collaborate cross-functionally to support ...

IQVIA, Inc.

Clinical Trial Lead

Durham, NC · On-site

... statistics, pharmacokinetics, clinical operations) and facilitate Trial Oversight Meetings. • Collaborate cross-functionally to support milestone achievement and proactively manage study risks and ...

Spyglass Pharma

Clinical Trial Associate

Irvine, CA · On-site

$35.75 - $48.75/hr

Knowledge of GCP and industry best practices with clinical trial management, monitoring, regulatory compliance, data management and statistical reporting. * Knowledge of US clinical and regulatory ...

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

Lead interdisciplinary core trial teams (e.g., data management, statistics, pharmacokinetics, clinical operations) and facilitate Trial Oversight Meetings. Collaborate cross-functionally to support ...

Spyglass Pharma

Clinical Trial Associate

Irvine, CA · On-site

$90K - $110K/yr

Knowledge of GCP and industry best practices with clinical trial management, monitoring, regulatory compliance, data management and statistical reporting. * Knowledge of US clinical and regulatory ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

Knowledge of GCP and industry best practices with clinical trial management, monitoring, regulatory compliance, data management and statistical reporting. * Knowledge of US clinical and regulatory ...

Parexel

Global Clinical Trial Leader - FSP

Seeking Clinical Trial Leaders in the US with Oncology and/or Inflammation Experience The Clinical ... Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring) * Verifies and ...

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Clinical Trial Statistician information

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$50.5K

$86.9K

$116.5K

How much do clinical trial statistician jobs pay per year?

As of Aug 21, 2026, the average yearly pay for clinical trial statistician in the United States is $86,921.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $98,500.00 per year, depending on experience, location, and employer.

What is a clinical trial statistician?

Clinical Trial Statisticians are professionals who design, analyze, and interpret data from clinical trials in the healthcare and pharmaceutical industries. They ensure that clinical studies are scientifically sound and that the results are statistically valid. Their work helps determine whether new treatments or medications are effective and safe. Clinical Trial Statisticians collaborate closely with researchers, clinicians, and regulatory agencies throughout the clinical trial process.

How do clinical trial statisticians typically collaborate with clinical research teams throughout a study?

Clinical Trial Statisticians play a key collaborative role by working closely with clinical researchers, data managers, and regulatory specialists. They are involved from the study design phase, providing input on statistical methodologies and sample size calculations, to ongoing data monitoring and final analysis. Regular meetings and clear communication are essential, as statisticians must translate complex statistical concepts for non-technical team members and ensure data integrity. This teamwork helps ensure the study's scientific validity and regulatory compliance.

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

To thrive as a Clinical Trial Statistician, you need a strong background in statistics or biostatistics, experience with clinical research, and typically a master's or PhD in a relevant field. Proficiency in statistical software such as SAS, R, or Python, and familiarity with regulatory guidelines like ICH-GCP are essential. Outstanding analytical thinking, attention to detail, and effective communication skills help in interpreting data and collaborating with cross-functional teams. These skills ensure accurate data analysis, regulatory compliance, and impactful contributions to the development of safe and effective medical treatments.

What is the difference between Clinical Trial Statistician vs Data Analyst in the clinical research industry?

AspectClinical Trial StatisticianData Analyst
Required CredentialsTypically requires a degree in statistics, biostatistics, or related field; often with certification in clinical researchUsually needs a degree in statistics, data science, or related field; certification is optional
Work EnvironmentWorks primarily in clinical research settings, hospitals, or pharmaceutical companies on clinical trial dataWorks across various industries, including healthcare, finance, or tech, often in office or remote settings
Employer & Industry UsageCommonly employed by pharmaceutical companies, CROs, and research institutionsEmployed across multiple sectors, including healthcare, finance, and technology

While both roles involve data analysis, a Clinical Trial Statistician specializes in designing and analyzing clinical trial data within the pharmaceutical and healthcare industry, whereas a Data Analyst has a broader scope across various industries. The Clinical Trial Statistician's focus on clinical research makes their skills and certifications more specialized for this field.

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What states have the most Clinical Trial Statistician jobs?

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What job categories do people searching Clinical Trial Statistician jobs look for?

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Clinical Trial Statistician jobs near you
Infographic showing various Clinical Trial Statistician job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $86,921 per year, or $41.8 per hour.

Expert Clinical Manager

Artech Information System LLC

East Hanover, NJ • On-site

Full-time

Re-posted 3 days ago

Job description

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

Job Description:
In collaboration with Trial Statistician, support of Reporting and Analysis Planning (RAP) modules in line with program standards.
Responsible to support development of and implementation of relevant data capture tools in collaboration with CSD, GTL and AQS as documented in data handling plan or equivalent document (e.g. CRFs protocol deviations, questionnaires, diaries, translation, edit checks)
Responsible for performing the ongoing review of clinical trial data as outlined in the data handling plan or equivalent , supports GTL to prepare database lock; and performing data reconciliation along the whole trila duration in collaboration with management.
Collaborate with Medical Lead/BSL to identify and safety trends; and as needed, reports on trial data to safety and clinical boards (e.g. SMT,GCT and GPT)
In collaboration with Medical Lead/BSL or CSD/CSAD, responsible for final analysis and interpretation of results including the development and drafting of clinical trial reports, publications and internal/external presentations.
Provide Support for biomarkers planning and or execution
May serve on or lead global process improvement work streams or act as Subject Matter Experts for training or SOP
May support CSD in limited program level activities

Qualifications
Skills:
Basic knowledge in planning, executing, reporting and publishing global clinical studies in a pharmaceutical company or contract research organization. Work experience in clinical operations preferable.
Strong interpersonal skills
Ability to work under pressure
Excellent negotiation and conflict resolution skills
Collaborates across boundaries for shared success
Resolve issues with minimal supervision and understand when to escalate
Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and clinical development process
Strong analytical / computational background
Demonstrates excellent Medical / scientific writing skills
Demonstrates knowledge and application of statistical analysis methodology and can identify trends and analyze / interpret / report data effectively
Education:
Advanced degree in life sciences/healthcare (or clinically relevant degree) is required.
PharmD, PhD or MD preferable.


Additional Information

Neha Sharma
Lead Recruiter
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960
Office: 973.967.3437 | Fax:  973.998.2599
Website: www.artechinfo.com



Artech logo

About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992

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