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Biostatistics R Jobs (NOW HIRING)

Formation Bio

Senior Director, Biostatistics

Boston, NY · On-site

$311K - $388K/yr

Lead and develop the Biostatistics team, fostering a high-performance culture aligned with ... Proficiency in SAS, R (S-Plus), and statistical software for sample size calculations (e.g., East ...

Geisinger

Biostatistician

Danville, PA · On-site +1

The Biostatistics Core at Geisinger collaborates closely with researchers across the health system ... Experienced SAS or R programmer for both data manipulation and statistical analysis. * Detail ...

Geisinger Health

Biostatistician

Danville, PA · On-site

The Biostatistics Core at Geisinger collaborates closely with researchers across the health system ... Experienced SAS or R programmer for both data manipulation and statistical analysis. * Detail ...

Verastem

Senior Director Biostatistics

Boston, MA · On-site

$250K - $300K/yr

Serve as a biostatistics leader within the organization, and manage statistical efforts for ... Proficient in statistical programming (SAS is required and R is a plus) * Experience with clinical ...

MSD

Senior Scientist, Biostatistics

North Wales, PA · On-site

SAS and/or R. Strong oral and written communication skills. Able to function effectively in a team ... Biostatistics, Business Decisions, Clinical Trials, Clinical Trials Analysis, Data Management, Data ...

MSD

Senior Scientist, Biostatistics

Rahway, NJ · On-site

SAS and/or R. Strong oral and written communication skills. Able to function effectively in a team ... Biostatistics, Business Decisions, Clinical Trials, Clinical Trials Analysis, Data Management, Data ...

MSD

Sr. Scientist, Biostatistics

North Wales, PA · On-site

SAS and/or R. * Good oral and written communication skills. Able to work effectively with personnel ... Biostatistics, Data Management, Data Science, Drug Discovery Process, Scientific Modeling ...

Spyre Therapeutics

OR · On-site

$290K/yr

Role Summary The Sr. Director of Biostatistics will provide leadership and strategic input for ... Proficiency in statistical software (e.g., SAS, R) and data management systems. * Experience with ...

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How much do biostatistics r jobs pay per hour?

As of Jul 7, 2026, the average hourly pay for biostatistics r in the United States is $49.00, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $61.54 per hour, depending on experience, location, and employer.

Is biostatistics in high demand?

Biostatistics is a growing field with strong demand due to the increasing need for data analysis in healthcare, pharmaceuticals, and research organizations. Biostatisticians with skills in statistical software like R and SAS are particularly sought after, especially in clinical trials and public health projects.

What jobs pay $500,000 a year in the US?

In biostatistics, senior roles such as biostatistics directors or chief statisticians at large pharmaceutical or biotech companies can reach or exceed $500,000 annually, especially with bonuses and stock options. These positions typically require extensive experience, advanced degrees, and expertise in statistical programming, clinical trial design, and regulatory compliance.

What jobs can you get with a biostatistics degree?

A biostatistics degree prepares individuals for roles such as biostatistician, clinical data analyst, epidemiologist, or research scientist. These jobs typically involve analyzing health data, designing studies, and using statistical software like R or SAS in healthcare, pharmaceutical, or public health settings.

What jobs make $1,000,000 a year?

In biostatistics, reaching a $1,000,000 annual salary is rare and typically involves senior roles such as chief data officer, biotech executive, or consultant with extensive experience and a strong reputation. High earnings may also come from consulting, entrepreneurship, or leadership positions in pharmaceutical or healthcare companies, often requiring advanced degrees, specialized skills, and industry connections.

Director, Biostatistics

Summit Therapeutics

Palo Alto, CA

Other

Re-posted 6 days ago

Job description

Overview of Role:

Serves as the project level biostatistician and provides leadership within biostatistics function to develop and execute statistical strategy, study design, statistical analyses, and regulatory submissions for clinical trials in oncology. Partners with clinical science, regulatory and other team members in clinical development plans, authoring key clinical/regulatory/statistical documents, and ensuring exceptional delivery and interpretation of clinical data. Develops and implements biostatistics department policies, standards, procedures, and work-instructions in coordination with department leader and other functions. Represents biostatistics function in interactions with CROs, institutional review boards, and regulatory agencies.

Role and Responsibilities:

  • Provide technical leadership and statistical support to clinical development through the design and conduct of clinical studies in oncology
  • Support/contribute to protocol development to ensure appropriateness of trial design, sample size, and propose the use of meaningful and efficient statistical methodologies
  • Lead development of statistical analysis plans, data presentation plans, clinical development plans, biometrics related submission activities, and post-submission strategies/responses
  • Review the accuracy of clinical data, perform statistical analysis, interpret study results, and collaborate with clinical team and other team members to produce interim reports, final reports, and publications
  • Write/review sections of meeting packages and assist in the development and review of other documents required for regulatory submissions and other regulatory processes
  • Review vendor data transfer specifications and ADaM programming specifications
  • Lead assessment and introduction of novel statistical methodologies to implement solutions
  • Represent biostatistics function or biometrics department in cross function teams
  • Work with department leader to develop and implement department policies, standards and procedures
  • Collaborate with clinical operations, data management and CRO to develop and implement CRFs, database design, and the overall data quality plan
  • Evaluate and manage CROs and other vendors, including scope-of-work, timelines, deliverables and budgets
  • Provide strategic statistical and regulatory guidance to anticipate challenges, mitigate risk, and ensure project success
  • Attend meetings with FDA or other health authorities to ensure ongoing agreement on project development
  • All other duties as assigned

Experience, Education and Specialized Knowledge and Skills:

  • PhD and a minimum of 8+ years of experience or Masters (MS) and a minimum of 11+ years of experience in statistics or biostatistics or related disciplines with clinical trials, pharmaceutical/biotech industry, or healthcare experience
  • Experience in supporting oncology phase II/III clinical studies
  • Experience in organizing and driving regulatory submissions (e.g. NDA, sNDA, BLA)
  • In-depth knowledge of CDISC standards
  • Technical expertise and knowledge of experimental design and analyses using SAS, R, or EAST, and etc.
  • Excellent written and verbal communication skills
  • Good working knowledge of ICH, FDA and GCP regulations and guidelines

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