1

Clinical R Programmer Jobs in Cordova, TN (NOW HIRING)

Biostatistician

Memphis, TN · On-site

$86.32 - $154.96/hr

... faculty, clinicians, population scientists, and/or laboratory scientists to develop study ... Strong foundation in statistical and data science methods, with experience in programming (e.g., R ...

New

Lead-Biostatistician

Memphis, TN · On-site

$114 - $216/hr

The successful candidate will work closely with Biostatistics faculty, collaborating clinical ... Strong foundation in statistical and data science methods, with experience in programming (e.g., R ...

New

next page

Showing results 1-20

Clinical R Programmer information

See Cordova, TN salary details

$21

$56

$89

How much do clinical r programmer jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical r programmer in Cordova, TN is $56.61, according to ZipRecruiter salary data. Most workers in this role earn between $46.83 and $64.09 per hour, depending on experience, location, and employer.

What is a Clinical R programmer?

Clinical R Programmers are professionals who use the R programming language to manage, analyze, and visualize clinical trial data in the pharmaceutical, biotech, or healthcare industries. They play a key role in preparing statistical reports, generating tables, listings, and figures (TLFs), and ensuring data integrity for regulatory submissions. Clinical R Programmers collaborate with statisticians, data managers, and clinical teams to ensure the accuracy and compliance of clinical trial results with industry standards and regulatory requirements.

What skills and qualifications are needed to be a Clinical R programmer?

To thrive as a Clinical R Programmer, you need a solid background in statistics, R programming, and clinical trial data analysis, often supported by a degree in statistics, biostatistics, or a related field. Expertise in SAS, CDISC standards (SDTM/ADaM), and familiarity with clinical data management systems are commonly required. Attention to detail, problem-solving skills, and effective communication enable you to interpret data accurately and collaborate with cross-functional teams. These skills are vital for ensuring reliable statistical outputs that support regulatory submissions and data-driven decisions in clinical research.

What are common challenges faced by Clinical R programmers when working with clinical trial data?

Clinical R Programmers often encounter challenges such as handling large and complex datasets, ensuring strict compliance with regulatory standards (like CDISC SDTM and ADaM), and maintaining data integrity throughout the analysis process. Collaboration can be demanding, as programmers must frequently coordinate with biostatisticians, data managers, and clinical teams to interpret data requirements and resolve discrepancies. Staying updated with evolving industry guidelines and managing tight project timelines are also common aspects of the role.

What is the difference between Clinical R Programmer vs Clinical SAS Programmer?

AspectClinical R ProgrammerClinical SAS Programmer
Required CredentialsTypically requires a degree in statistics, biostatistics, or related field; proficiency in R programmingUsually requires a degree in statistics, biostatistics, or related field; proficiency in SAS programming
Work EnvironmentOften works in research-focused settings, academia, or biotech companies using open-source toolsCommonly employed in pharmaceutical companies, CROs, and clinical trial data analysis using SAS
Industry UsageGrowing in popularity for data analysis and visualization in clinical researchStandard in clinical trial data management and regulatory submissions

While both roles involve programming for clinical data analysis, Clinical R Programmers focus on using R for statistical analysis and visualization, whereas Clinical SAS Programmers primarily use SAS for data management and reporting. The choice depends on the company's preferred tools and project requirements.

What are popular job titles related to Clinical R Programmer jobs in Cordova, TN?

For Clinical R Programmer jobs in Cordova, TN, the most frequently searched job titles are:

What cities near Cordova, TN are hiring for Clinical R Programmer jobs?

Cities near Cordova, TN with the most Clinical R Programmer job openings:

Postdoctoral Research Associate - Statistical Methods for Pediatric Oncology Clinical Trials

St. Jude Children's Research Hospital

Memphis, TN • On-site

$65 - $85/hr

Other

Posted 2 days ago

New


Key responsibilities

  • Develop innovative statistical methods for pediatric oncology clinical trials.

  • Analyze clinical trial, registry, and real-world datasets related to pediatric oncology.

  • Collaborate with pediatric oncologists, clinical investigators, statisticians, and data scientists on trial design and analysis.


St. Jude Children's Research Hospital rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

42nd of 1,065 rated hospitals


Job description

Postdoctoral Research Associate - Statistical Methods for Pediatric Oncology Clinical Trials

Location

Memphis, TN

Category

Postdoc

Department

Shift

Weekday Day

Position Type

Full Time

Scheduled Weekly Hours

40

JR7572

Job Description

We are seeking a highly motivated Postdoctoral Researcher to develop innovative statistical methods for pediatric oncology clinical trials.

The research program focuses on methodological challenges arising in pediatric and rare-disease settings, where patient populations are often small, outcomes may be delayed or complex, and conventional randomized trial approaches may not always be feasible. The successful candidate will work at the intersection of innovative clinical trial design, causal inference, external controls and real-world evidence, digital twins and counterfactual prediction, and statistical methods for survival, longitudinal, and other complex outcomes.

Clinical applications will focus primarily on pediatric solid tumors, including neuroblastoma and sarcoma, as well as emerging cellular and immunotherapy studies such as CAR-T therapy.

The position provides substantial flexibility for the postdoctoral researcher to develop an independent methodological research program based on the candidate’s background and interests, emerging scientific opportunities, and important problems arising from ongoing pediatric oncology research.

Research Areas

Potential areas of methodological research include:

Innovative Clinical Trial Design

Development of efficient and rigorous statistical methods for early- and mid-phase pediatric oncology trials, particularly in settings involving small populations, rare diseases, heterogeneous treatment response, or delayed outcomes.

Causal Inference, External Controls, and Real-World Evidence

Development of principled approaches for incorporating external information into clinical trials when concurrent randomized control groups are limited or infeasible.

Digital Twins and Counterfactual Prediction

An emerging research direction is the development and evaluation of digital twins and counterfactual prediction methods for clinical trials.

Rather than viewing a digital twin solely as a prediction model, we are interested in understanding when model-based predictions can provide clinically and statistically credible information about outcomes under alternative treatment strategies.

Survival, Longitudinal, and Complex Clinical Outcomes

Many pediatric oncology trials involve delayed, longitudinal, multistate, or otherwise complex outcomes that motivate new statistical methodology.

Your Role

The postdoctoral researcher will have opportunities to:

  • Develop new statistical methodology motivated by important pediatric oncology problems
  • Conduct simulation studies to evaluate statistical operating characteristics
  • Analyze clinical trial, registry, and real-world datasets
  • Develop statistical software in R and/or Python
  • Collaborate closely with pediatric oncologists, clinical investigators, statisticians, and data scientists
  • Participate in the design and analysis of innovative pediatric oncology clinical trials
  • Publish methodological and applied research in leading statistical, clinical trial, and medical journals
  • Present research at national and international scientific meetings
  • Develop independent research ideas and a coherent methodological research program
  • Contribute to collaborative grant proposals and future independent funding applications
  • Participate in mentoring and research activities within the Department of Biostatistics

The balance between methodological development and applied collaboration can be tailored to the candidate’s background, interests, and career goals.

Requirements

We are looking for a candidate with strong quantitative training who is interested in developing statistical methodology motivated by challenging clinical problems.

Ideal candidates will have:

  • A PhD in biostatistics, statistics, epidemiology, data science, or a closely related quantitative discipline
  • Strong training in statistical methodology
  • Experience with statistical programming, preferably in R and/or Python
  • Strong written and oral communication skills
  • Ability to work effectively in multidisciplinary research teams
  • Interest in clinical trials and biomedical research

Experience in one or more of the following areas would be particularly valuable:

  • Clinical trial design
  • Survival analysis
  • Bayesian statistics
  • Causal inference
  • External controls or real-world evidence
  • Target trial emulation
  • Longitudinal data analysis
  • Machine learning or causal prediction
  • Pediatric oncology

Prior experience in pediatric oncology is not required. Candidates with strong methodological training who are interested in developing expertise in pediatric cancer research are encouraged to apply.

St. Jude is an Equal Opportunity Employer

No Search Firms

St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.

#J-18808-Ljbffr

What St. Jude Children's Research Hospital employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom