ZipRecruiter

Log In

1

Contract Biostatistics Jobs (NOW HIRING)

Sumitomo Pharma

Associate Director, Biostatistics

$165K - $207K/yr

Serve as the biostatistics lead for one or more studies within a project team, offering expertise ... Plan, manage, and supervise the statistical activities conducted by Contract Research Organizations ...

Cherokee Federal

Biostatistician

Aberdeen, MD · On-site

A government contract requires that this position be restricted to U.S. citizens or legal permanent ... Master's preferred in Biostatistics or related field. * Minimum of 3 years of research-related ...

Actalent

Biostatistician

Seattle, WA · On-site +1

$140K - $170K/yr

... grants and contracts. * Contribute to research in statistical methods and represent the ... PhD in Statistics, Biostatistics, or a related field. * Minimum of two years of relevant experience ...

Unicon Pharma Inc.

Biostatistician II

Basking Ridge, NJ · On-site

... oversee contract research organization (CRO) programmers and statisticians for analysis file ... PhD or Master's in statistics or biostatistics. - Essential skills: Clinical research, clinical ...

Apply Early

CICONIX, LLC

Biostatistician I

San Antonio, TX · On-site

Master's in Biostatistics or related field. * Experience: * Minimum 1 year using SAS or statistical ... This opportunity is contingent and will begin upon contract award. CICONIX LLC is an Equal ...

CICONIX, LLC

Biostatistician I

Bexar, TX

Master's in Biostatistics or related field. * Experience: * Minimum 1 year using SAS or statistical ... This opportunity is contingent and will begin upon contract award. CICONIX LLC is an Equal ...

Apply Early

next page

Showing results 1-20

All JobsContract Biostatistics Jobs

Contract Biostatistics information

See salary details

$12

$57

$107

How much do contract biostatistics jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for contract biostatistics in the United States is $57.79, according to ZipRecruiter salary data. Most workers in this role earn between $29.57 and $80.05 per hour, depending on experience, location, and employer.

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

To thrive as a Contract Biostatistician, you need a solid background in statistics or biostatistics, often backed by an advanced degree and experience with clinical trial data analysis. Proficiency in statistical programming languages like SAS or R, as well as familiarity with regulatory requirements and data management systems, is essential. Strong analytical thinking, attention to detail, and effective communication skills help you interpret complex data and collaborate with multidisciplinary teams. These skills are crucial for ensuring the accuracy of study results and supporting critical decision-making in clinical research.

What is the difference between Contract Biostatistics vs Clinical Data Management?

AspectContract BiostatisticsClinical Data Management
Required CredentialsBiostatistics degree, statistical certificationsHealth sciences, data management certifications
Work EnvironmentCollaborates with statisticians, research teamsData entry, database management teams
Employer & Industry UsagePharmaceuticals, biotech, research organizationsClinical trial sites, CROs, pharma companies

Contract Biostatistics focuses on analyzing clinical trial data and statistical reporting, while Clinical Data Management involves collecting, cleaning, and maintaining trial data. Both roles are essential in clinical research but differ in their core responsibilities and skill sets.

What are some common challenges faced by contract biostatisticians, and how can they be managed?

Contract biostatisticians often navigate challenges such as quickly adapting to diverse projects, working with varying data standards, and integrating into new teams remotely or on short notice. Managing these challenges requires strong communication skills, adaptability, and a solid understanding of regulatory guidelines. Building a robust professional network and staying updated on industry best practices can also help contract biostatisticians excel and deliver high-quality results in dynamic environments.

What are Contract Biostatistics?

Contract biostatistics refers to statistical analysis and consulting services provided by professionals or firms on a contract basis, typically for pharmaceutical, biotechnology, or medical research organizations. These biostatisticians are responsible for designing studies, analyzing clinical trial data, and ensuring compliance with regulatory standards. Companies often outsource these roles to gain specialized expertise, flexibility, and cost-effectiveness for specific projects without hiring full-time staff.
What cities are hiring for Contract Biostatistics jobs? Cities with the most Contract Biostatistics job openings:
What are the most commonly searched types of Biostatistics jobs? The most popular types of Biostatistics jobs are:
What states have the most Contract Biostatistics jobs? States with the most job openings for Contract Biostatistics jobs include:
What job categories do people searching Contract Biostatistics jobs look for? The top searched job categories for Contract Biostatistics jobs are:
Contract Biostatistics jobs near you
Infographic showing various Contract Biostatistics job openings in the United States as of June 2026, with employment types broken down into 4% Temporary, and 96% Contract. Highlights an 58% Physical, 3% Hybrid, and 39% Remote job distribution, with an average salary of $120,211 per year, or $57.8 per hour.
Director Biostatistics - Oncology

Director Biostatistics - Oncology

Penfield Search Partners

San Francisco, CA • On-site

Other

Posted 23 days ago

Job description

Job Description Our client is a clinical-stage biopharma company focusing in the Oncology space. They are currently seeking a highly skilled and experienced Director of Biostatistics to provide leadership to develop and execute statistical strategy, design and analyses for clinical trials in all phases. As Director you will apply sound statistical methodology to meet project objectives, health authority guidelines, and regulatory requirements.

This is onsite role based in the Bay Area. About the Role: Provide leadership within biostatistics function to develop and execute statistical strategy, design and analyses for clinical trials in all phases. Apply sound statistical methodology to meet project objectives, health authority guidelines, and regulatory requirements.

Develop and/or applies statistical theories, methods and software. Partner in clinical development program, study design, establishing standards for clinical conduct, and the collection, management and/or reporting of data. Provide strategic statistical and regulatory guidance to anticipate challenges, mitigate risk, and ensure project success.

Represent biostatistics function in interactions with institutional review boards, ethics committees, and health agencies. Work with department head to develop and implement department standards and practices. Direct the statistical design, conduct, and analysis of clinical trials in all phases.

Review protocols and case report forms for soundness of trial design. Review and or author statistical analysis plans for all phases of a trial. Perform analysis, interpret study results, and collaborate with clinical team to produce interim reports, final reports, and publications.

Direct the development, validation and summary of integrated safety and efficacy summaries. Interact with FDA or EU Authority staff to ensure clinical studies meet regulatory requirements. Attend meetings with FDA or EU Authority to ensure ongoing agreement on project development.

Contribute to the development of Requests-for-Proposals. Evaluate and manage contract research organizations and other vendors, including scope-of-work, timelines, deliverables and budgets. Responsible for all statistical oversight within a therapeutic area.

Please have: MS/MS degree in Statistics/Biostatistics and 10 years' industry experience or PhD and 7 years. Comprehensive and detailed knowledge of: statistical experimental designs, analyses and clinical trial requirements, particularly pertaining to Oncology trials. Developed/reviewed SDTM/ADaM specifications.

Excellent knowledge of FDA/EU statistical guidelines. Experience in state-of-the-art data organization and statistical analyses using statistical software such as: R and SAS. Understanding of other disciplines such as data management, clinical operations, clinical science, regulatory affairs and drug safety.

Project management and contract negotiation with outside vendors.

Apply