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Clinical R Programmer Jobs in Tennessee (NOW HIRING)

Patient Care Specialist

Clarksville, TN · On-site

$15.75 - $20/hr

Fior & Gentz, an innovative developer of neuro orthotics; and College Park, creators of custom ... Maintains professional relationships with patients, referral sources, clinical and non-clinical ...

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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 does a clinical programmer do?

A clinical programmer develops and maintains software for clinical trials, including programming data collection, validation, and analysis tools. They work with statistical teams to generate reports and ensure data accuracy, often using programming languages like SAS or R in a regulated environment.

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.

Is clinical SAS programmer a good career?

A clinical SAS programmer is a specialized role in the healthcare and pharmaceutical industries, focusing on data analysis and reporting using SAS software. It offers stable employment, competitive salaries, and opportunities for advancement, especially with certifications and experience. The role typically requires strong analytical skills and knowledge of clinical trial processes.

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 is the salary of a clinical data programmer?

The salary of a clinical data programmer typically ranges from $70,000 to $100,000 annually, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced professionals with advanced skills in SAS, R, or SQL can earn higher salaries. Many roles also offer benefits such as health insurance and flexible schedules.

Which is better, CDM or SAS?

For a Clinical R Programmer, SAS is a widely used statistical software in clinical trials and regulatory submissions, offering robust data management and analysis capabilities. CDM (Clinical Data Management) refers to the process of handling clinical data, often using tools like SAS or dedicated CDM systems; the choice depends on project needs, but SAS proficiency is highly valued in the field.
What cities in Tennessee are hiring for Clinical R Programmer jobs? Cities in Tennessee with the most Clinical R Programmer job openings:
R&D Technician - Nonwoven (4533)

R&D Technician - Nonwoven (4533)

NICE-PAK PRODUCTS LLC

Smyrna, TN

Full-time

Posted 15 days ago


Job description

Summary:

The Laboratory Technician position is an integral role within the Nice Pak R&D organization, providing technical testing and laboratory support for private label and branded wet wipe projects. The responsibilities of the role include, but are not limited to, conducting laboratory experiments, batching of formulations, technical and stability testing of products, raw material and competitive product analyses, sample preparation for consumer and clinical tests, and general laboratory supply and housekeeping duties. This role will have the opportunity to work on a variety of product types including baby, toddler, facial, personal care, hand and surface wipes.

Essential Duties and Responsibilities:

· Performance Measurements:

o Achievement: Ability to deliver technical work on time, without issue and in a quality manner.

o Ownership: Ability to demonstrate strong ownership of assigned projects and project work – ability to work independently.

o Partnership Skills: Ability to work well cross-functionally, communicate effectively and work as part of a team to achieve objectives.

o Entrepreneurial Skills: Ability to problem solve if issues arise and propose potential solutions

· Technical testing of wet and dry wipes to ensure product performance, efficacy, quality and stability

· Laboratory batching of prototype and final formulations (liquid formula, nonwoven, packaging) for clinical and consumer studies, testing and customer review

· Perform dispersibility testing of Moist Toilet Tissue (MTT) products to evaluate flushable performance

· Conduct and contribute to the development of new test methods; record, summarize and report data accurately to supervisor and project teams

· Evaluate and analyze competitive products

· Prepare samples and conduct employee panel evaluations of wet wipe prototypes and products

· Support Scientists and Engineers with manufacturing line trial and production scale-up activities

· Maintain and calibrate laboratory equipment including balances, pH meters, viscometers, etc.

· Order and maintain chemicals and laboratory supplies ensuring proper storage, labeling and disposal as needed

· Ensure a clean laboratory and working environment, following all corporate Health and Safety protocols

· Manage time independently, ensure proper documentation in laboratory notebook and comply with all corporate safety and quality standards

· Supervise any assigned temporary personnel

Education Requirements:

Minimum high school diploma required; 2-year associate degree in a technical/science field preferred

Experience Requirements:

· Relevant experience in R&D and Science fields

Competencies:

· Computer literate, Outlook, Word, Excel

· Strong written and verbal communication skills

· Team player with strong interpersonal skills

· Ability to display flexibility and adapt to changes

· Good time management skills with the ability to work on multiple projects of various scope, size and complexity

· Ability to understand and generate statistical data, graphs, and tables

· Strong problem-solving skills with root-cause analysis

· Ability to quantify test results and analyze them to create meaningful reports

· Ability to read and write technical documents

· Able to work in a fast-paced environment and manage multiple simultaneous experiments or tasks across projects

Certificates, Licenses, Registrations:

None

Travel:

Limited

Work Environment:

This job operates in a professional laboratory and office environment. This role routinely uses standard laboratory equipment and standard office equipment such as hot plates, pH meter, viscometer, Ross miles foam height apparatus, mixers, balances, computers, phones, photocopiers, filing cabinets and fax machines.

Physical Demands:

Occasionally lift boxes of product 5-50 lbs. Frequently lift samples 1-5 lbs. Walking, talking, hearing, climbing, reaching, grasping, and standing. Clarity of vision at 20 inches or less, with the ability to distinguish colors and adjust eye to bring objects into sharper focus.