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Clinical R Programmer Jobs in Pennsylvania (NOW HIRING)

Atorus Research

Sr R & SAS Programmer

Chesterbrook, PA · On-site

Knowledge of R programming in clinical trials Familiarity of the drug development process. Knowledge of CDISC standards and electronic submission requirements. Strong SAS and SAS Macro language ...

Geisinger

Biostatistician

Danville, PA · On-site +1

Possesses the critical thinking skills needed to provide statistical support to clinical investigators. * Experienced SAS or R programmer for both data manipulation and statistical analysis. * Detail ...

Geisinger Health

Biostatistician

Danville, PA · On-site

Possesses the critical thinking skills needed to provide statistical support to clinical investigators. * Experienced SAS or R programmer for both data manipulation and statistical analysis. * Detail ...

Certara USA, Inc.

Senior SAS Developer

Wayne, PA · On-site

Responsibilities As a Statistical Programming Consultant, you will use your SAS and R programming ... At least 6 years of Clinical trials related work experience in SAS programming, analysis and ...

Atorus Research

Principal Biostatistician

Malvern, PA · On-site

... clinical studies -Solid background of statistics -Experience of SAS, R and other statistical programming packages to validate key endpoint analysis. -Possess extensive knowledge of the Drug ...

Globusmedical

Manufacturing Engineer

Eagleville, PA · On-site

$72K - $93K/yr

Our passion, combined with Globus' world-class engineering, transforms clinical insights into ... Utilize statistical and quality tools such as Gage R&R, Cp/Cpk, and SPC to assess and improve ...

Globus Medical

Manufacturing Engineer

Eagleville, PA · On-site

$72K - $93K/yr

Our passion, combined with Globus' world-class engineering, transforms clinical insights into ... Utilize statistical and quality tools such as Gage R&R, Cp/Cpk, and SPC to assess and improve ...

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Clinical R Programmer information

What are the key skills and qualifications needed to thrive as a Clinical R Programmer, and why are they important?

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 Clinical R Programmers?

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 are some 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 Pennsylvania? For Clinical R Programmer jobs in Pennsylvania, the most frequently searched job titles are:
What job categories do people searching Clinical R Programmer jobs in Pennsylvania look for? The top searched job categories for Clinical R Programmer jobs in Pennsylvania are:
What cities in Pennsylvania are hiring for Clinical R Programmer jobs? Cities in Pennsylvania with the most Clinical R Programmer job openings:
Clinical R Programmer jobs near you

Sr R & SAS Programmer

Atorus Research

Chesterbrook, PA • On-site

Contractor

Re-posted 21 days ago

Job description

Sr SAS & R Programmer
onsite in the Chesterbrook, PA area 3 days/week
SUMMARY
The contract Senior Statistical Programmer is a member of the Biometrics Department within the Research and Development (R&D) organization who supports Statistical programming work in accordance with corporate standard operating procedures (SOPs), GCP, 21 CFR and ICH guidance.
RESPONSIBILITIES
Program and validate derived datasets, tables, figures, listings. Process data from the external sources.
Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other organizations.
Oversee programing work/deliverables from CROs.
Contribute to the design/implementation/review of Case Report Form, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages.
Program and validate CDISC compliant deliveries for the electronic submissions.
Support in the creation of supporting documentation for submissions.
Ensure programming deliverables are on time and of high quality.
Help managing internal contractors and external vendors.
Participate in development of departmental working instructions and guidelines.
Help in creation of enhanced functions/macros and utilities.
REQUIREMENTS
Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline.
BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry.
Working knowledge of SAS and its various components.
Knowledge of R programming in clinical trials
Familiarity of the drug development process.
Knowledge of CDISC standards and electronic submission requirements.
Strong SAS and SAS Macro language skills.
R programming skills in clinical trials
Strong knowledge of industry standards.
Ability to work on data integrations (ISS and ISE).
Strong oral and written communication skills. Ability to communicate details of the analysis to other team members with less technical experience.
Ability to manage the timeline well and work in multi-project environment.

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