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Clinical R Programmer Jobs in Oregon (NOW HIRING)

Cytel

Senior Clinical Programmer

Salem, OR · On-site

Proficient in clinical data programming languages (e.g., SAS, R, SQL, etc.). * Expertise in clinical programming platforms, including experience with clinical data workflows, data integration, and ...

Kite Pharma

OR

$107K - $138K/yr

Kite Pharma, a Gilead company, is a clinical-stage biopharmaceutical company focused on the ... Extensive experience with statistical programming using the SAS and R software including ...

Exactsciences

Clinical Biostatistician I

OR · On-site +1

$71/hr

Position Overview The Clinical Biostatistician collaborates with interdisciplinary, cross ... Strong statistical programming skills (SAS, R, or Python). * Basic computer skills to include ...

Amgen

OR

... R programming for clinical trial analyses, data manipulation, reporting and visualization preferred Familiarity with additional programming languages and tools such as Python preferred Hands-on ...

Natera

OR · On-site

This is an exciting opportunity to lead Natera's Statistical Programming team, specifically focused ... Expert working knowledge of R for clinical trial reporting; experience maintaining statistical ...

Arcus Biosciences

$245K - $260K/yr

An advanced degree in Pharmaceutics/Pharmacy/Engineering/Statistics with demonstrated expertise in ... Expertise with standard modelling and simulation software (NONMEM, S-Plus/R, etc) is required.

Amgen

OR · On-site

Career Category Clinical Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're ... Match programmer abilities to tasks. Efficiently and optimally monitor and utilize assigned staff

Syneoshealth

OR

Our Clinical Solutions team members act with a drug development mindset, applying their years of ... R packages in the OHDSI/DARWIN ecosystem (for cohort execution, characterization, estimation, and ...

Syneoshealth

OR · On-site

Our Clinical Solutions team members act with a drug development mindset, applying their years of ... SAS or R, Must have SQL experience. * Programmatic Cohort derivation experience * Index date ...

Exactsciences

OR · On-site

$102K - $153K/yr

The Clinical Biostatistician II with general guidance from more experienced Statisticians, works ... Strong statistical programming skills (SAS, R, or Python). * Strong verbal, written, and graphical ...

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

Senior Clinical Programmer

Cytel

Salem, OR • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

We are seeking an experienced and skilled Clinical Programmer with a strong background within clinical programming. The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position requires a solid understanding of clinical trials, data integration, and programming techniques to support the creation, validation, and execution of clinical study data in a fast-paced environment.

Key Responsibilities:

  • Programming and Development: Write and maintain code for clinical trial data processes, including data extraction, transformation, and analysis using the multiple programming environment.
  • Data Management and Quality: Ensure accurate and timely delivery of clinical trial data by performing data checks, validation, testing, and reconciliation in line with clinical trial timelines and regulatory requirements.
  • Collaboration: Work closely with clinical data managers, statisticians, and other stakeholders to design and implement clinical data flow, ensuring compliance with all regulatory requirements.
  • Troubleshooting and Issue Resolution: Identify, investigate, and resolve any issues that arise within the platform or clinical data programming processes.
  • Documentation: Maintain comprehensive documentation of programming processes, code, and data management workflows for audit and regulatory purposes.
  • Continuous Improvement: Contribute to the improvement of programming practices, tools, and templates to streamline clinical programming workflows and enhance efficiency.
  • Training and Mentorship: Provide guidance and mentorship to junior programmers, ensuring adherence to best practices and facilitating knowledge sharing within the team.
  • Experience: 4-6 years of experience in clinical programming.
  • Technical Skills:
  • Proficient in clinical data programming languages (e.g., SAS, R, SQL, etc.).
  • Expertise in clinical programming platforms, including experience with clinical data workflows, data integration, and programming solutions.
  • Strong knowledge of clinical trial data structures, data standards (e.g., CDISC, SDTM), and regulatory requirements (e.g., FDA, EMEA).
  • Problem-Solving: Excellent troubleshooting and problem-solving skills with the ability to work under pressure to meet deadlines.
  • Communication: Strong communication skills with the ability to collaborate effectively with cross-functional teams and communicate technical concepts to non-technical stakeholders.
  • Education: Bachelor's degree or higher in Computer Science, Life Sciences, Engineering, or related field (or equivalent work experience).

Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.

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