Senior Clinical Programmer
$145K - $156K/yr
Position Summary The Senior Clinical Programmer at ReCor Medical requires complete knowledge and full understanding of clinical programming principles and practices for medical device clinical trials.
$145K - $156K/yr
Position Summary The Senior Clinical Programmer at ReCor Medical requires complete knowledge and full understanding of clinical programming principles and practices for medical device clinical trials.
$145K - $156K/yr
Position Summary The Senior Clinical Programmer at ReCor Medical requires complete knowledge and full understanding of clinical programming principles and practices for medical device clinical trials.
Boston, MA · On-site
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 ...
Boston, MA · On-site
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 ...
Boston, MA · 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 · 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 ...
We're looking for a Senior Clinical Programmer I who thrives on solving complex challenges and transforming clinical data into high-quality, reliable insights that drive drug development. In this ...
We're looking for a Senior Clinical Programmer I who thrives on solving complex challenges and transforming clinical data into high-quality, reliable insights that drive drug development. In this ...
Raleigh, NC · 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 · 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 ...
Pleasanton, CA · On-site
$139K - $149K/yr
The Position Roche Molecular Systems, Inc. seeks a Senior Clinical Programmer at its Pleasanton, California location. Duties: Develop software solutions for statistical modeling and analysis of ...
Pleasanton, CA · On-site
$139K - $149K/yr
The Position Roche Molecular Systems, Inc. seeks a Senior Clinical Programmer at its Pleasanton, California location. Duties: Develop software solutions for statistical modeling and analysis of ...
Bridgewater, NJ · Remote
$75 - $80/hr
Join a growing clinical programming function within a science-driven biopharmaceutical organization developing therapies for patients with serious and rare diseases. This newly established team is ...
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Bridgewater, NJ · Remote
$75 - $80/hr
Join a growing clinical programming function within a science-driven biopharmaceutical organization developing therapies for patients with serious and rare diseases. This newly established team is ...
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King Of Prussia, PA · 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 ...
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King Of Prussia, PA · 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 ...
Pasadena, CA · On-site
$120K - $140K/yr
... programmer, preferably within a CRO or a similar group. Prior management experience is not needed. They will initially contribute their expertise in the area of data management/clinical or ...
Pasadena, CA · On-site
$120K - $140K/yr
... programmer, preferably within a CRO or a similar group. Prior management experience is not needed. They will initially contribute their expertise in the area of data management/clinical or ...
Los Angeles, CA · On-site
$120K - $140K/yr
... programmer, preferably within a CRO or a similar group. Prior management experience is not needed. They will initially contribute their expertise in the area of data management/clinical or ...
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Los Angeles, CA · On-site
$120K - $140K/yr
... programmer, preferably within a CRO or a similar group. Prior management experience is not needed. They will initially contribute their expertise in the area of data management/clinical or ...
Fairfield, CT · On-site +1
Neisha Camacho/Terra Parsons - No 3rd party candidates Position Summary We are seeking an experienced Senior Clinical Programmer to support clinical development programs by delivering high-quality ...
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Fairfield, CT · On-site +1
Neisha Camacho/Terra Parsons - No 3rd party candidates Position Summary We are seeking an experienced Senior Clinical Programmer to support clinical development programs by delivering high-quality ...
Fairfield, CT · On-site +1
Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.com No 3rd party candidates Position Summary We are seeking an experienced Senior Clinical Programmer to support clinical development programs by ...
Fairfield, CT · On-site +1
Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.com No 3rd party candidates Position Summary We are seeking an experienced Senior Clinical Programmer to support clinical development programs by ...
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 ...
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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 ...
Chantilly, VA · 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 ...
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Chantilly, VA · 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 ...
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 ...
Newark, NJ · On-site
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 ...
Newark, NJ · On-site
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 ...
Redmond, WA · On-site
$100K - $150K/yr
Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer ... The EDC Programmer (EDCP) is a critical technical role responsible for building, configuring, and ...
Redmond, WA · On-site
$100K - $150K/yr
Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer ... The EDC Programmer (EDCP) is a critical technical role responsible for building, configuring, and ...
Redmond, WA · On-site
$100K - $150K/yr
Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer ... The EDC Programmer (EDCP) is a critical technical role responsible for building, configuring, and ...
Quick apply
Redmond, WA · On-site
$100K - $150K/yr
Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer ... The EDC Programmer (EDCP) is a critical technical role responsible for building, configuring, and ...
S. or Canada Contract/Corp to Corp JOB OVERVIEW The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating, deploying and maintaining clinical databases and ...
S. or Canada Contract/Corp to Corp JOB OVERVIEW The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating, deploying and maintaining clinical databases 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 ...
$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.

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 Senior Clinical Programmer at ReCor Medical requires complete knowledge and full understanding of clinical programming principles and practices for medical device clinical trials. Responsible for designing, developing, and maintaining clinical data management systems that support regulatory submissions and ensure data integrity throughout clinical trials. Works independently to solve diverse problems related to clinical data processing, applying sophisticated analytical techniques to identify and resolve complex issues. Collaborates with cross-functional teams while providing technical guidance on clinical data processing methodologies.
Responsibilities and Duties
Design and develop custom applications, scripts, and tools for clinical data collection, processing, and analysis
Establish and enforce data standardization practices (e.g., CDISC, SDTM, ADaM)
Collaborate with cross-functional teams including clinical operations, biostatistics, and regulatory affairs
Assess unusual circumstances and use sophisticated analytical techniques to identify and resolve complex data issues
Generate reports and visualizations for clinical studies
Program, validate, and maintain table listings and figures (TLFs) for clinical study reports and regulatory submissions
Create and maintain data integration pipelines between clinical systems and internal databases
Provide technical guidance to junior programmers on clinical data processing methodologies
Other Duties as assigned.
Requirements
Bachelor's degree in computer science, statistics, life sciences, or a related field with a minimum of 5 years of related experience; or Master's degree with 3 years of experience; or equivalent work experience.
Proficiency in R, with experience in other relevant programming languages (e.g., Python, SQL, SAS).
Comprehensive understanding of clinical trial processes, data flow, and clinical trial data standards (e.g., CDISC SDTM, ADaM).
Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and explain technical concepts to non-technical stakeholders.
Knowledge of regulatory requirements and experience preparing programming deliverables for submissions to regulatory agencies.
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: $145,604- $156,347 (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.
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Medical equipment and supplies manufacturing
11 - 50 Employees
Palo Alto, CA, US
2009