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Clinical R Programmer Jobs in Los Angeles, CA (NOW HIRING)

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Summary The Clinical Program Manager shall oversee comprehensive programming for a housing unit based in the Hollywood section of Los Angeles with a focus on co-occurring populations. Primary duties ...

BCBA Clinical Supervisor

South Gate, CA · On-site

$75K - $91K/yr

Conduct developmental skills assessments, such as (not limited to) the ABLLS-R, AFLS, and/or VB ... programming and/or behavioral recommendations, implementing training as necessary, and providing ...

BCBA Clinical Supervisor

Downey, CA · On-site

$77K - $94K/yr

Conduct developmental skills assessments (e.g., ABLLS-R, AFLS, VB-MAPP) to create and evaluate ... programming and behavioral recommendations, implementing necessary training, and offering ongoing ...

Conduct developmental skills assessments, such as ABLLS-R, AFLS, and/or VB-MAPP, to develop and ... programming and behavioral recommendations, implementing necessary training, and offering regular ...

BCBA Clinical Supervisor

Culver City, CA · On-site

$81K - $99K/yr

Conduct developmental skills assessments, such as ABLLS-R, AFLS, and/or VB-MAPP, to create and ... Collaborate with school personnel by conducting student observations, providing written programming ...

BCBA Clinical Supervisor

Santa Ana, CA · On-site

$77K - $94K/yr

Conduct developmental skills assessments, such as ABLLS-R, AFLS, and/or VB-MAPP, to create and ... programming and behavioral recommendations, implementing necessary training, and offering regular ...

BCBA Clinical Supervisor

Los Angeles, CA · On-site

$79K - $97K/yr

Conduct developmental assessments, such as ABLLS-R, AFLS, and/or VB-MAPP, to create and evaluate ... Collaborate with school staff by observing students, providing written programming and behavioral ...

Showing results 21-40

Clinical R Programmer information

See Los Angeles, CA salary details

$26

$69

$110

How much do clinical r programmer jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for clinical r programmer in Los Angeles, CA is $69.80, according to ZipRecruiter salary data. Most workers in this role earn between $57.74 and $78.99 per hour, depending on experience, location, and employer.

What skills and qualifications are needed to be a Clinical R programmer?

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 is a Clinical R programmer?

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

Senior Field Clinical Engineer - NMPH - Remote within USA

Medtronic

Northridge, CA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago


Medtronic rating

7.9

Company rating: 7.9 out of 10

Based on 175 frontline employees who took The Breakroom Quiz

159th of 536 rated manufacturers


Job description

We anticipate the application window for this opening will close on - 8 Aug 2026
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the Life
Join a diverse team of innovators who bring their worldview, their unique backgrounds and their individual life experiences to work every day. It's no accident - we work hard to cultivate a workforce that reflects our patients and partners. We believe it's the only way to drive healthcare forward and remain a global leader in medical technology and solutions. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work.
As a Senior Field Clinical Engineer (FCE), you will play a critical role in supporting clinical studies and advancing neuromodulation technologies. This position serves as a technical bridge between engineering, clinical research teams, and physicians to ensure successful study implementation, high-quality data collection, and effective use of investigational and commercial devices. The primary focus of the role is supporting clinical trials while providing clinical insights that help improve existing products and guide development of new technologies.
Responsibilities may include the following and other duties may be assigned.
  • Support all phases of clinical research studies, including investigator identification, site nomination, activation, training, enrollment support, and study close-out.
  • Provide on-site technical support during clinical procedures and initial product implants, evaluating device performance in the clinical setting.
  • Serve as a liaison between engineering, clinical research teams, and physicians to ensure proper device use and protocol adherence.
  • Monitor study progress and support sites in maintaining high-quality data collection and documentation.
  • Build and maintain strong relationships with investigators and clinical teams to understand capabilities, research interests, and patient needs.
  • Provide feedback to engineering and R&D teams to support product improvements and development of new technologies.
  • Collaborate with clinical research partners on study protocols, execution, and documentation.
  • Educate internal teams, sales partners, and customers on technology, clinical applications, and best practices, particularly during product launches.

Location: Remote within US
Remote: We are seeking a committed professional to join our team, required to reside within the region and drive or fly to multiple accounts throughout the US. A valid driver's license is essential for this role, which also involves 70% - 75% amount of travel outside the region, presenting opportunities for broader engagement.Occasional work across multiple time zones .
Ability to travel up to: 70-75% domestically with some international travel
Must Have (Minimum Requirements)
To be considered for this role, please ensure the minimum requirements are evident on your resume.
  • Bachelor's degree and 4 years of experience in clinical research/clinical or as a clinical specialist/field clinical engineer/clinical sales rep or
  • Advanced degree and 2 years of experience in clinical research/clinical or as a clinical specialist/field clinical engineer/clinical sales rep

Nice to Have (Preferred Qualifications)
  • Experience at Medtronic or within the medical device industry
  • Experience in the management of clinical devices
  • Neuromodulation or Pelvic Health device training strongly preferred
  • Experience in biomedical engineering, hospital/clinic and/or medical sales
  • 2+ years of experience in clinical research, Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trials

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD):$108,000.00 - $162,000.00
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

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