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Clinical R Programmer Jobs in Troy, OH (NOW HIRING)

... clinical notes, patient feedback, and medical literature, to extract meaningful insights ... Lead development from prototype through production in partnership with engineering/architecture.

Calibration Technician

Vandalia, OH · On-site

$20.75 - $28.25/hr

Our clients range from growing biotech firms advancing groundbreaking clinical trials to ... We offer a variety of fields to embark in, including manufacturing, engineering, quality, chemistry ...

Calibration Technician

Vandalia, OH

$20.75 - $28.25/hr

Our clients range from growing biotech firms advancing groundbreaking clinical trials to ... We offer a variety of fields to embark in, including manufacturing, engineering, quality, chemistry ...

Our clients range from growing biotech firms advancing groundbreaking clinical trials to ... We offer a variety of fields to embark in, including manufacturing, engineering, quality, chemistry ...

Our clients range from growing biotech firms advancing groundbreaking clinical trials to ... We offer a variety of fields to embark in, including manufacturing, engineering, quality, chemistry ...

Clinical R Programmer information

See Troy, OH salary details

$22

$59

$94

How much do clinical r programmer jobs pay per hour?

As of May 30, 2026, the average hourly pay for clinical r programmer in Troy, OH is $59.47, according to ZipRecruiter salary data. Most workers in this role earn between $49.23 and $67.31 per hour, depending on experience, location, and employer.

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 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 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 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 cities near Troy, OH are hiring for Clinical R Programmer jobs? Cities near Troy, OH with the most Clinical R Programmer job openings:

Manager, Chemistry Group, R&D

Xylem

Yellow Springs, OH

Full-time

Posted 18 days ago


Xylem rating

7.3

Company rating: 7.3 out of 10

Based on 83 frontline employees who took The Breakroom Quiz

298th of 511 rated manufacturers


Job description

Xylem is a Fortune 500 global water solutions company dedicated to advancing sustainable impact and empowering the people who make water work every day. As a leading water technology company with 23,000 employees operating in over 150 countries, Xylem is at the forefront of addressing the world's most critical water challenges. We invite passionate individuals to join our team, dedicated to exceeding customer expectations through innovative and sustainable solutions.

We're Hiring a Manager for our Chemistry Group, R& D in Yellow Springs!

This position will serve as the manager of the chemistry group within R&D. The position contributes technical oversight of all group activities and embraces a hands-on approach to laboratory analytical chemistry. As our Chemistry interface between R&D and other departments, the position will provide visibility and accountability into R&D efforts towards new product release or sustainment of multiple major product lines and systems. This individual works in tandem with assigned new product Project Managers and our Sustainment Manager. Products/Projects include Life Science Biochemical Analyzers, enzyme/membrane-based sensing technology, and environmental monitoring systems. This role reports directly to the Director, R&D - YSI.

Job Specifications and Work Performed:

Provide oversight for a small team of analytical chemists by:

Working closely with team members by taking a hands-on approach to lead the execution of technology development into innovative products.

Assure all laboratory operations comply with regulatory and Xylem safety standards.

Managing day-to-day performance of direct reports.

Providing mentorship and constructive feedback to direct reports on completion of goals.

  • Authority to sign Engineer Change Orders and Engineering Drawings for all chemistry releases.
  • Participate as a peer on the R&D Staff Management Team to provide transparency and accountability of group efforts, and communicate needs and dependencies to other development groups, sustainment groups, and project managers within R&D.
  • Determine theoretical and practical limitations to sensing specifications through laboratory experimentation and R&D prototype builds.
  • Proper design of experiment methodology to support proof of concept and sensor validation including FDA regulated validation practices and relevant consensus standard guidelines for In Vitro Diagnostic Devices.
  • Responsible for driving efficiencies into and expanding Chemistry team involvement in new product development or sustaining projects.
  • Responsible for chemistry derived documentation and deliverables satisfying the Xylem New Product Development stage/gate process.
  • Collection, analysis and publication of Chemistry Group Key Performance Indicators (KPI) and Metrics. Provide monthly results of KPIs to the Director.
  • Achieving new product development plan objectives, including meeting required technical specifications, meeting cost targets and delivering on schedule.
  • Assure the accuracy, clarity, internal integrity, consistency, and timeliness of all technical information submitted.
  • Drive continuous improvements into scientific/engineering/manufacturing processes and policies.
  • Provide interpretation, guidance and strategies on technologies and methodologies affecting product approvals, development and continued product compliance.
  • Assessing and evaluating new and existing technologies that are opportunities or threats.
  • Work closely with relevant cross-functional areas to achieve overall product development success as needed (operations/manufacturing and quality, marketing and sales, customer service, finance, and technical support).
  • Assume other activities and responsibilities as directed.

Experience & Academic Requirements

  • Graduate degree in biochemistry, biotechnology or biochemical engineering or related scientific discipline.
  • 7+ years of hands on engineering or science work experience in a multidiscipline R&D environment.
  • 2+ years supervisory experience
  • Proven ability to deliver new technology/products to the market.

Key Skills and Attributes

  • Excellent written and oral communication skills.
  • Ability to develop and deliver effective presentations.
  • Ability to multi-task effectively.
  • Participative management style that advocates team concept.
  • Process & resource planning, with particular consideration to the challenges of creativity and innovation.
  • Strong analytical, reasoning, leadership and team interaction skills.
  • Capable of using computer-based tools to collect and document project work and facilitate responsibilities.
  • Ability to recruit, train and motivate personnel to balance staffing strength with profitability and growth.
  • Familiarity with FDA 510(k) clinical validation studies and prior experience with human blood product handling.
  • Knowledge of Investigational Review Boards and the ethics of human subject involvement.
  • Poise, good judgment and confidence to represent the Company.
  • Ability to work with a diverse workforce and customer base.
  • Ensures compliance with Company's and regulatory policies and procedures.

Working Condition:

  • Minimum 8 hours/day
  • 5-10% travel
  • General office/laboratory environment. This role is local and on-site at our offices in Yellow Springs, Ohio, however some work may be able to be carried out in Hybrid fashion with Director approval.

Join the global Xylem team to be a part of innovative technology solutions transforming water usage, conservation, and re-use. Our products impact public utilities, industrial sectors, residential areas, and commercial buildings, with a commitment to providing smart metering, network technologies, and advanced analytics for water, electric, and gas utilities. Partner with us in creating a world where water challenges are met with ingenuity and dedication; where we recognize the power of inclusion and belonging in driving innovation and allowing us to compete more effectively around the world.

At Xylem, you'll not only contribute to solving water issues but also have the chance to make a difference through our paid Volunteer Program, Xylem Watermark. We prioritize our employees' well-being through inclusion and belonging as well as our Employee Resource Groups (ERG). Proud to be an Equal Employment Opportunity (including disability and veterans) and Affirmative Action workplace, Xylem fosters an inclusive environment free from discrimination or harassment.

Please note that the information in this job description outlines the general nature of the position and is not an exhaustive list of duties. Xylem is dedicated to providing reasonable accommodations to enable all employees to perform their essential job functions. We reserve the right to modify this job description and assign additional duties as needed. Embrace the opportunity to be part of Xylem's transformative journey in shaping the future of water technology! #XylemCareers #GlobalImpact #WaterInnovation


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