Clinical Programmer II
Palo Alto, CA ยท On-site
Position Summary The Clinical Programmer II at Recor Medical develops and maintains advanced programming solutions for clinical trial data management, analysis, and reporting. This role requires ...
Palo Alto, CA ยท On-site
Position Summary The Clinical Programmer II at Recor Medical develops and maintains advanced programming solutions for clinical trial data management, analysis, and reporting. This role requires ...
Palo Alto, CA ยท On-site
Position Summary The Clinical Programmer II at Recor Medical develops and maintains advanced programming solutions for clinical trial data management, analysis, and reporting. This role requires ...
Palo Alto, CA ยท On-site
Position Summary The Clinical Programmer II at Recor Medical develops and maintains advanced programming solutions for clinical trial data management, analysis, and reporting. This role requires ...
Palo Alto, CA ยท On-site
Position Summary The Clinical Programmer II at Recor Medical develops and maintains advanced programming solutions for clinical trial data management, analysis, and reporting. This role requires ...
Boston, MA ยท On-site
... non-statistical clinical reporting and implement these reports with high quality and on time. This position is responsible for taking a lead role in SAS programming support of centralized ...
Boston, MA ยท On-site
... non-statistical clinical reporting and implement these reports with high quality and on time. This position is responsible for taking a lead role in SAS programming support of centralized ...
Raleigh, NC ยท On-site +1
Principal Clinical Programmer Job Code: CDM0016 Department Name: Clinical Data Management Reports to Title: Manager or above Job Summary: The Principal Clinical Programmer is a member of the Data ...
Raleigh, NC ยท On-site +1
Principal Clinical Programmer Job Code: CDM0016 Department Name: Clinical Data Management Reports to Title: Manager or above Job Summary: The Principal Clinical Programmer is a member of the Data ...
Possesses expert knowledge in SAS programming and can mentor, train, develop clinical programmers in using SAS to perform complex data handling and non-statistical clinical data reporting Possesses ...
Possesses expert knowledge in SAS programming and can mentor, train, develop clinical programmers in using SAS to perform complex data handling and non-statistical clinical data reporting Possesses ...
$60K - $70K/yr
Clinical Applications Programmer II Salary Range : $60,000-70,000 Location : Baltimore, MD About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping ...
$60K - $70K/yr
Clinical Applications Programmer II Salary Range : $60,000-70,000 Location : Baltimore, MD About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping ...
Baltimore, MD ยท On-site
$60K - $70K/yr
Clinical Applications Programmer II Salary Range : $60,000-70,000 Location : Baltimore, MD About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping ...
Baltimore, MD ยท On-site
$60K - $70K/yr
Clinical Applications Programmer II Salary Range : $60,000-70,000 Location : Baltimore, MD About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping ...
Be Seen First
King Of Prussia, PA ยท Remote
$90K - $150K/yr
Qualifications: * 5+ years of EDC database build experience for clinical trial. * Experience with Medidata Rave with Medidata certification; Minimum two to three years current database programming ...
Quick apply
Be Seen First
King Of Prussia, PA ยท Remote
$90K - $150K/yr
Qualifications: * 5+ years of EDC database build experience for clinical trial. * Experience with Medidata Rave with Medidata certification; Minimum two to three years current database programming ...
Clinical Applications Programmer IISalary Range: $60,000-70,000Location: Baltimore, MDAbout PharmaronPharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma ...
Clinical Applications Programmer IISalary Range: $60,000-70,000Location: Baltimore, MDAbout PharmaronPharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma ...
Chantilly, VA ยท Remote
Clinical SAS Programmer No of positions- 2 Location- Remote Experience Required:6+ Years Education: Bachelor's degree in Computer Science, Computer Engineering, or related technical field Job Summary ...
Quick apply
Chantilly, VA ยท Remote
Clinical SAS Programmer No of positions- 2 Location- Remote Experience Required:6+ Years Education: Bachelor's degree in Computer Science, Computer Engineering, or related technical field Job Summary ...
SAS Programmer II / Clinical Trials / Remote Work Duration: 21 months contract, extendable up to 24 Months Location: Remote Worker Client Location: Memphis, TN Note: The client has the right-to-hire ...
Quick apply
SAS Programmer II / Clinical Trials / Remote Work Duration: 21 months contract, extendable up to 24 Months Location: Remote Worker Client Location: Memphis, TN Note: The client has the right-to-hire ...
Provides input in the design and development of case report forms and clinical databases. * Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers ...
Provides input in the design and development of case report forms and clinical databases. * Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers ...
Performs all SAS programming required for clinical trial analysis and reporting. * Ensures that activities and processes performed are conducted according to sponsor requirements. * Works closely ...
Performs all SAS programming required for clinical trial analysis and reporting. * Ensures that activities and processes performed are conducted according to sponsor requirements. * Works closely ...
Designs and implements global library and study specific setup for clinical trials applications ... Programmers that might assist in building studies to ensure all jobs are carried out and timelines ...
Designs and implements global library and study specific setup for clinical trials applications ... Programmers that might assist in building studies to ensure all jobs are carried out and timelines ...
Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Programmer . You will be responsible for administration of EDC Database including evaluation ...
Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Programmer . You will be responsible for administration of EDC Database including evaluation ...
The Associate Clinical SAS Programmer/Junior Statistician plays a pivotal role in the clinical trial lifecycle by transforming raw clinical trial data into formatted, analysis-ready datasets and ...
The Associate Clinical SAS Programmer/Junior Statistician plays a pivotal role in the clinical trial lifecycle by transforming raw clinical trial data into formatted, analysis-ready datasets and ...
The Associate Clinical SAS Programmer/Junior Statistician plays a pivotal role in the clinical trial lifecycle by transforming raw clinical trial data into formatted, analysis-ready datasets and ...
The Associate Clinical SAS Programmer/Junior Statistician plays a pivotal role in the clinical trial lifecycle by transforming raw clinical trial data into formatted, analysis-ready datasets and ...
Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Programmer . You will be responsible for administration of EDC Database including evaluation ...
Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Programmer . You will be responsible for administration of EDC Database including evaluation ...
OR ยท Remote
Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Programmer . You will be responsible for administration of EDC Database including evaluation ...
Quick apply
OR ยท Remote
Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Programmer . You will be responsible for administration of EDC Database including evaluation ...
Oversees system-wide clinical application projects related to pharmacy services and overviews the interfaces of pharmacy systems integration with other hospital systems * Participates in on-going ...
Oversees system-wide clinical application projects related to pharmacy services and overviews the interfaces of pharmacy systems integration with other hospital systems * Participates in on-going ...
$24.76 - $31.84
3% of jobs
$31.84 - $38.92
4% of jobs
$38.92 - $46
9% of jobs
$46 - $53.08
5% of jobs
$54.30 is the 25th percentile. Wages below this are outliers.
$53.08 - $60.16
17% of jobs
The median wage is $63.26 / hr.
$60.16 - $67.24
25% of jobs
$71.78 is the 75th percentile. Wages above this are outliers.
$67.24 - $74.32
17% of jobs
$74.32 - $81.40
9% of jobs
$81.40 - $88.48
6% of jobs
$88.48 - $95.56
2% of jobs
$95.56 - $102.64
1% of jobs
$24
$64
$102
| Aspect | Clinical Programmer | Data Manager |
|---|---|---|
| Required Credentials | Bachelor's degree in life sciences, computer science, or related field; programming skills in SAS, R, or SQL | Bachelor's degree in health sciences, statistics, or related field; experience with data management software |
| Work Environment | Collaborates with statisticians, data managers, and clinical teams to develop and validate data reports | Oversees data collection, validation, and database management for clinical trials |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Pharmaceutical companies, CROs, clinical research organizations |
While both Clinical Programmers and Data Managers work within clinical research, Clinical Programmers primarily focus on developing data reports and programming analysis datasets, whereas Data Managers handle data collection, validation, and database management. Both roles require strong analytical skills and familiarity with clinical data standards, often working closely together to ensure data quality and integrity in clinical trials.
Cities with the most Clinical Programmer job openings:
States with the most job openings for Clinical Programmer jobs include:
The top searched job categories for Clinical Programmer jobs are:
For Clinical Programmer jobs, the most frequently searched job titles are:

Palo Alto, CA โข On-site
Full-time
Posted 15 days ago
At Recor Medical, we are pioneering Ultrasound Renal Denervation (uRDN) therapy to treat hypertension, the leading cardiovascular risk factor in the world. With our Paradise uRDN System, we're on a mission to provide the millions of people who suffer from hypertension with a non-drug and minimally invasive option to lower their blood pressure. Join us on our journey and make a meaningful impact on the lives of people around the globe.
Position Summary
The Clinical Programmer II at Recor Medical develops and maintains advanced programming solutions for clinical trial data management, analysis, and reporting. This role requires strong proficiency in R and/or SAS and understanding of clinical trial processes and operational metrics. Key responsibilities include performing complex data analysis, generating reports, and creating tools to support both clinical research and operational decision-making. The ideal candidate will collaborate with cross-functional teams, mentor junior programmers, and contribute to process improvements. They will demonstrate technical expertise, problem-solving skills, and the ability to work independently and collaboratively, while staying current with industry trends and maintaining high standards of quality and compliance.
Responsibilities and Duties
Design, develop, validate, and maintain complex programs to support clinical trial data management processes, including data integration, transformation, and analysis using R, SAS, or other relevant programming languages.
Perform advanced data analysis and generate complex reports, tables, listings, and figures to support clinical trial data review, statistical analysis, regulatory submissions, and operational decision-making.
Support clinical operational activities by developing and maintaining tools for tracking study progress, site performance, and other key operational metrics, including generating regular reports and dashboards to provide insights into clinical trial operations.
Collaborate with cross-functional teams to implement statistical analysis plans and design programming solutions that address specific project requirements.
Troubleshoot complex data issues and propose solutions to ensure data integrity and quality throughout the clinical development process.
Conduct programming peer reviews, provide technical guidance, and mentor junior programmers to ensure code quality and adherence to standards.
Participate in version control using Git and maintain comprehensive documentation for scripts, packages, and applications.
Contribute to the development of study documentation, including programming specifications and data management plans.
Lead process improvement initiatives to enhance efficiency and quality in clinical programming activities.
Stay abreast of emerging trends, technologies, and industry standards (e.g., CDISC) in clinical programming and data management, implementing improvements as appropriate and assisting in preparing for regulatory audits and inspections.
Other duties as assigned
Requirements
Master's degree in computer science, data science, statistics, life sciences, or related field with 1+ years of experience; or a Bachelor's degree in these fields with 2+ years of professional experience in Clinical Programming, data visualization, business intelligence, or analytics roles.
Strong proficiency in R and/or SAS, with experience in other relevant programming languages and tools (e.g., Python, SQL).
Demonstrated ability to identify and resolve performance bottlenecks and optimize code for efficiency and scalability.
Experience in extracting, cleaning, transforming, and loading data from diverse sources, managing datasets, and ensuring data quality and integrity.
Understanding of clinical trial processes and data flow from study setup to database lock.
Working knowledge of clinical trial data standards (e.g., CDISC SDTM, ADaM) is strongly preferred.
Experience with or understanding of clinical trial operations and associated metrics is highly desirable.
Excellent problem-solving and analytical skills, with the ability to translate complex requirements into efficient programming solutions.
Experience with version control systems (e.g., Git) and collaborative development practices.
Familiarity with tools and techniques for visualizing operational data and creating interactive dashboards (e.g., Tableau, Power BI) is a plus.
Ability to mentor junior team members, including conducting code reviews and providing technical guidance.
Strong written and verbal communication skills, with the ability to explain technical concepts to non-technical stakeholders.
Demonstrated ability to work independently and collaboratively in a fast-paced environment.
Commitment to continuous learning and staying updated with emerging trends in clinical programming and data analysis.
Preferred Skills
Experience with data visualization tools (e.g., Power BI, Tableau)
Proficiency in version control systems (e.g., Git) and collaborative development practices
Experience mentoring junior programmers and conducting code reviews
Familiarity with cloud-based data platforms and integration technologies
Experience with software validation per FDA guidelines
Knowledge of machine learning or advanced analytics techniques applicable to clinical data
Salary range: $122,857 - $132,796 (Annual Base Salary)
The successful candidate's starting base pay will be determined based on job-related skills, experience, qualifications, work location and market conditions. The expected base pay range for this role may be modified based on market conditions.
Equal Employment Opportunity
At Recor Medical, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.
Pre-Employment Requirements
At Recor Medical, patient safety, integrity, and regulatory compliance are foundational to everything we do. To support these standards,employmentis contingent upon meeting the following requirements:
Radiation Safety Requirement
Certain field-based roles at Recor Medical require work in environments where radiation sources (e.g., x-ray equipment) are in use. Employees in these roles will be issued a personal dosimetry badge to monitor occupational exposure and are required to wear it in accordance with company policy and applicable regulatory standards. This program is designed to ensure compliance with federal and state regulations and to maintain radiation exposure at levels that are As Low As Reasonably Achievable (ALARA). Additional guidance and protective equipment, as necessary, will be provided as part of onboarding and ongoing safety training.
Respecting your privacy is an essential part of the Company's privacy program and we are committed to the proper handling of Personal Information collected or processed in connection with an Applicant's application for employment, a Contract Worker's work, or a Former Employee's employment at Recor. Refer to our Applicant, Contract Worker & Former Employee Privacy Policy for more detail information.
Sourced by ZipRecruiter
Medical equipment and supplies manufacturing
11 - 50 Employees
Palo Alto, CA, US
2009