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HomeCompaniesIblyjb Fa Ocs Oraclecloud Com CX 2001Senior Clinical Programmer

Senior Clinical Programmer

Iblyjb Fa Ocs Oraclecloud Com CX 2001 · United States; United States - Remote - Eastern Time, Cambridge, MA, US · Remote · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyIblyjb Fa Ocs Oraclecloud Com CX 2001
TitleSenior Clinical Programmer
Normalized title-
Department / teamClinical Programming
LocationUnited States
Work modelRemote / Remote
Employment typeFull Time
Salary-
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-04-23 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

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PageWhat it containsOpen
Company jobsActive postings from Iblyjb Fa Ocs Oraclecloud Com CX 2001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Oracle Recruiting Cloud / Fusion HCM.Open
Provider filtered searchThe same provider as a filtered job collection.Open
Department jobsActive postings in Clinical Programming.Open
Work model jobsActive Remote postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyIblyjb Fa Ocs Oraclecloud Com CX 2001
Source118dd8bd-c51f-43c2-93a6-817304220200
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description We are seeking an experienced and skilled Clinical Programmer with a strong background within clinical programming. The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position requires a solid understanding of clinical trials, data integration, and programming techniques to support the creation, validation, and execution of clinical study data in a fast-paced environment. Responsibilities Key Responsibilities: Programming and Development: Write and maintain code for clinical trial data processes, including data extraction, transformation, and analysis using the multiple programming environment. Data Management and Quality: Ensure accurate and timely delivery of clinical trial data by performing data checks, validation, testing, and reconciliation in line with clinical trial timelines and regulatory requirements. Collaboration: Work closely with clinical data managers, statisticians, and other stakeholders to design and implement clinical data flow, ensuring compliance with all regulatory requirements. Troubleshooting and Issue Resolution: Identify, investigate, and resolve any issues that arise within the platform or clinical data programming processes. Documentation: Maintain comprehensive documentation of programming processes, code, and data management workflows for audit and regulatory purposes. Continuous Improvement: Contribute to the improvement of programming practices, tools, and templates to streamline clinical programming workflows and enhance efficiency. Training and Mentorship: Provide guidance and mentorship to junior programmers, ensuring adherence to best practices and facilitating knowledge sharing within the team. Qualifications Experience: 4-6 years of experience in clinical programming. Technical Skills: Proficient in clinical data programming languages (e.g., SAS, R, SQL, etc.). Expertise in clinical programming platforms, including experience with clinical data workflows, data integration, and programming solutions. Strong knowledge of clinical trial data structures, data standards (e.g., CDISC, SDTM), and regulatory requirements (e.g., FDA, EMEA). Problem-Solving: Excellent troubleshooting and problem-solving skills with the ability to work under pressure to meet deadlines. Communication: Strong communication skills with the ability to collaborate effectively with cross-functional teams and communicate technical concepts to non-technical stakeholders. Education: Bachelor’s degree or higher in Computer Science, Life Sciences, Engineering, or related field (or equivalent work experience).

Full job record

Job ID78f673056a96c0e6f3e699d2d20e566ee687a75b
Org ID1db7e607-b344-4109-abb0-4cfac49e25b6
Source ID118dd8bd-c51f-43c2-93a6-817304220200
Board ID118dd8bd-c51f-43c2-93a6-817304220200
Provideroracle_hcm
Provider Job Key1482
TitleSenior Clinical Programmer
Normalized Title
Statusactive
Activeyes
Location TextUnited States; United States - Remote - Eastern Time, Cambridge, MA, US
DepartmentClinical Programming
Team
Employment Typefull_time
Workplace Typeremote
Remote Policyremote
CountryUnited States
Region
City
Salary RawDescription We are seeking an experienced and skilled Clinical Programmer with a strong background within clinical programming. The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position requires a solid understanding of clinical trials, data integration, and programming techniques to support the creation, validation, and execution of clinical study data in a fast-paced environment. Responsibilities Key Responsibilities: Programming and Development: Write and maintain code for clinical trial data processes, including data extraction, transformation, and analysis using the multiple programming environment. Data Management and Quality: Ensure accurate and timely delivery of clinical trial data by performing data checks, validation, testing, and reconciliation in line with clinical trial timelines and regulatory requirements. Collaboration: Work closely with clinical data managers, statisticians, and other stakeholders to design and implement clinical data flow, ensuring compliance with all regulatory requirements. Troubleshooting and Issue Resolution: Identify, investigate, and resolve any issues that arise within the platform or clinical data programming processes. Documentation: Maintain comprehensive documentation of programming processes, code, and data management workflows for audit and regulatory purposes. Continuous Improvement: Contribute to the improvement of programming practices, tools, and templates to streamline clinical programming workflows and enhance efficiency. Training and Mentorship: Provide guidance and mentorship to junior programmers, ensuring adherence to best practices and facilitating knowledge sharing within the team. Qualifications Experience: 4-6 years of experience in clinical programming. Technical Skills: Proficient in clinical data programming languages (e.g., SAS, R, SQL, etc.). Expertise in clinical programming platforms, including experience with clinical data workflows, data integration, and programming solutions. Strong knowledge of clinical trial data structures, data standards (e.g., CDISC, SDTM), and regulatory requirements (e.g., FDA, EMEA). Problem-Solving: Excellent troubleshooting and problem-solving skills with the ability to work under pressure to meet deadlines. Communication: Strong communication skills with the ability to collaborate effectively with cross-functional teams and communicate technical concepts to non-technical stakeholders. Education: Bachelor’s degree or higher in Computer Science, Life Sciences, Engineering, or related field (or equivalent work experience).
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://iblyjb.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/1482
Apply URLhttps://iblyjb.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/1482
First Seen At2026-05-31 17:57:23Z
Last Seen At2026-06-06 19:15:54Z
Last Checked At2026-06-06 19:15:54Z
Last Changed At2026-06-06 11:13:47Z
Inactive At
Source Posted At2026-04-23 11:13:39Z
Source Updated At
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