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Clinical R Programmer Jobs in New York (NOW HIRING)

By teaming up with clinicians, operations, and administrative teams, the individual will develop ... Proficiency in at least one programming language (Python, R) and machine learning tools ...

About Sanofi: We're an R&D-driven, AI-powered biopharma company committed to improving people ... Engineering, Pharmacy, Chemistry, Biology, etc.) ​ Experience & Technical Skills: * Experience in ...

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About Sanofi: We're an R&D-driven, AI-powered biopharma company committed to improving people ... Engineering, Pharmacy, Chemistry, Biology, etc.) ​ Experience & Technical Skills: * Experience in ...

New

About Sanofi: We're an R&D-driven, AI-powered biopharma company committed to improving people ... Engineering, Pharmacy, Chemistry, Biology, etc.) ​ Experience & Technical Skills: * Experience in ...

New

About Sanofi: We're an R&D-driven, AI-powered biopharma company committed to improving people ... Engineering, Pharmacy, Chemistry, Biology, etc.) ​ Experience & Technical Skills: * Experience in ...

New

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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 job categories do people searching Clinical R Programmer jobs in New York look for? The top searched job categories for Clinical R Programmer jobs in New York are:
What cities in New York are hiring for Clinical R Programmer jobs? Cities in New York with the most Clinical R Programmer job openings:
Principal Scientist, DDT-Lab Automation, Digital Lab and Automation Strategy

Principal Scientist, DDT-Lab Automation, Digital Lab and Automation Strategy

MSD

Rahway, NJ • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago


Job description

Job Description

Job Description: Principal Scientist, DSCS Digital Technologies-Laboratory Automation, Digital Lab and Automation Strategy

We are seeking a Principal Scientist to join our DSCS Digital Technologies (DDT) organization, within Development Sciences and Clinical Supply (DSCS), located in Rahway, NJ.

Primary Responsibilities:

We are a global biopharmaceutical leader with a portfolio of prescription medicines, oncology,vaccinesand animal health products. We are driven by our purpose to develop and deliver innovative products that save and improve lives. With 69,000 employeesoperatingin more than 140 countries, we offerstate-of-the-artlaboratories, plants and offices that are designed to inspire our employees as we learn,developand grow in our careers. We are proud of our over 125 years of service to humanity and continue to be one of the world's biggest investors in Research & Development.

In the Development Sciences and Clinical Supply (DSCS) organization, we believe digital is the force multiplier that enables faster experiments, smarter decisions, more robust supply chains, and isultimately redefininghow we bring medicines to patients.

Within DSCS, theDSCSDigital Technologies(DDT)teamis building the next generation of data-rich, connected lab environments-where hardware, software, and AI-driven tools work together to accelerate pharmaceutical development. Our goal is simple but ambitious: embed advanced digital capabilities into the DNA of how we work. We believe this future starts witha strong foundationof laboratory tools: innovative robotics,process analytical technology (PAT), high-throughput technologies,reliable instrumentation, and integrated systems that seamlessly transition data from the physical labs to the digital world. We believe innovation is fueled by teams that come together to buildtechnologiesthat trulyimpacthow our scientists conduct research.We'relooking for aPrincipal Scientistto help make this vision real.

In this role,the chosen candidatewill work with a team of scientists tasked withidentifying, developing, and deployingdigital and data-richtechnologiesaimed at improving themanner in whichprocess, product, and analyticalunderstanding is gathered. Thetoolsthatwe develop are as the team developing them, and in thisPrincipal Scientistrole,the chosen candidatewillleveragedigitaltechnologiestoenablechemistry, manufacturing, and controls (CMC)activitiesacrossour company's small molecule, biologics, and vaccines portfolio.This includes, but is not limited to, leading lab automation and high throughput technology initiativesvia the design, build, and maintenance of lab automation platforms and developing next-generation digitally integrated lab automation solutions to support current and future DSCS development.

HowYou'llMake an Impact

  • Design the lab of the futureby leading high throughputlab automation initiatives that integrate robotics,analyticalinstrumentation, and software into cohesive, high-performing solutions- leveraging digital tools (e.g. Agentic AI) where possible to enable rapid development cycles
  • Deliver world-renownedscienceby partnering with researchers to understand experimental needs and convert them into scalabledigitalworkflows
  • Work at the intersection ofmultipledisciplines, collaborating with experts in automation, data science, modeling, IT, andthe CMC community at large
  • Lead high-impact projectsfrom concept through deployment, working across teams and stakeholders to deliver meaningful outcomes
  • Continuously improveexistingdigital technologies and automation platformsto enhance performance, usability, and reliability
  • Empower othersby providing hands-onpartnership,support, troubleshooting, and training to scientists using thesetechnologies

Education Minimum Requirement:

  • Ph.D. in Chemical/Biochemical/Biomedical Engineering, Chemistry, Biology, Pharmaceutical Sciences, or a closely-related field with at least 6 years of industrial/pharmaceutical or relevant experience
  • M.S. in Chemical/Biochemical/Biomedical Engineering, Chemistry, Biology, Pharmaceutical Sciences, or a closely-related field with at least 8 years of industrial/pharmaceutical or relevant experience
  • B.S. in Chemical/Biochemical/Biomedical Engineering, Chemistry, Biology, Pharmaceutical Sciences, or a closely-related field with at least 10 years of industrial/pharmaceutical or relevant experience

Required Experience and Skills:

  • Demonstrated leadership experience in a lab-based setting, working with lab automation and equipment integration
  • Demonstrated leadership in designing, validating, optimizing, and operating robotic liquid handlers, robotic workcells, and other automation platforms
  • Experience with scripting/programming in one or more of the following: Python, C#, VBA, JavaScript, R, following accepted best practices (version control, design patterns, clean code)
  • Significant experience with one or more commercial lab automation platforms, specifically front-end software, such as: Tecan, Biomek, Formulatrix, Hamilton, or HighRes Biosolution liquid handlers
  • Experience integrating laboratory instruments with custom or commercial software solutions
  • Demonstrated ability to work in an entrepreneurial and independent manner while being a team player
  • Collaboration and communication skills with the ability to navigate conversations with technicians and vendors
  • Experience leading technical projects with cross-functional teams

Preferred Experience and Skills:

  • Experience with (bio)pharmaceutical process research and development (e.g. drug substance development, drug product development, and/ or analytical development)
  • Experience with Benchling, Signals, or other commercial laboratory notebook software
  • Experience with ThermoFisher Momentum, Biosero Green Button Go, or HighRes Biosolutions Cellario robotic scheduling software
  • Deep knowledge about laboratory automation software, firmware, hardware, and their integration into end-to-end solutions
  • Ability to recognize, prototype, and deploy innovative technologies in laboratory automation
  • Understanding of data science and AI/ML concepts and their application to laboratory automation


Required Skills:

Biomedical Engineering, Chemical Engineering, Computer Programming, Data Analysis, Innovative Thinking, Laboratory Automation, Manufacturing, Pharmaceutical Sciences, Professional Collaboration, Programming Languages, Robotic Liquid Handlers, Robotics Design

Preferred Skills:

C Sharp (Programming Language), Project Leadership, Python (Programming Language), R Programming

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is

$173,200.00 - $272,600.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

Domestic/International

VISA Sponsorship:

Yes

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

07/21/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.