Clinical ink
Clinical Programmer
Skills
2 months ago
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Important information
Contract type:
Permanent
Location:
United States
Work mode:
Onsite
Published on:
4 September 2026
What they need
Company Information Clinical Ink is the global life science company that brings data, technology, and patient science together to unlock clinical discovery. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancement, drive the industry standard for data precision and usher in a new generation of clinical trials. With offices in the United States and Denmark, Clinical Ink is rewriting the clinical development experience.
Job Description Clinical Ink is seeking a Clinical Programmer to join our Data Management team based remotely across the United States! This individual will develop, configure, and quality-check data integrations, exports, custom reports, and database scripts to ensure accurate and reliable customer data transfers. The role also troubleshoots data issues, communicates progress to stakeholders, and contributes to technical and process improvements throughout the project lifecycle. This role's responsibilities include:
Review and apply data mappings for customer specific data exports
Perform peer review / QC of data export programming
Produce data transfers via data export files and/or web services
Work with customers to specify data transfer standards and develop/implement software code to automate data transfer activities
Provide database programming support for custom reports
Perform peer review / QC of custom report programming
Create and implement database scripts to correct issues
Participate in departmental discussions regarding technical, functional and process improvement
Ensure that all project-related programming tasks are completed in accordance with standard practices throughout the lifecycle of the project including, but not limited to:
Perform data integration configuration, programming, and documentation
Process Data Clarification Forms (DCFs)
Manage and program targeted rules
Oversee data outputs for integrity and accuracy
Triage, research and provide solutions for identified data issues
Communicate progress and roadblocks on programming efforts to internal and external stakeholders
Assist junior staff to troubleshoot programming issues
Contribute to department knowledge share for common issues, standard processes, guides, etc.
Qualifications
- Bachelor’s degree in computer science, software engineering, information technology, informatics, or closely related field (or equivalent experience)
- 5+ years of experience as a software developer, database analyst/programmer, or clinical software tester
- Experience with Snowflake
- Experience building reports in SSRS, Tableau, or other reporting tools
- 2+ years’ experience with programming in Microsoft SQL and/or MySQL
- 3+ years of experience programming in SAS
- 5+ years of experience with Clinical Data Management and clinical development technology solutions
- Understanding of the clinical trial processes, including common data standards (CDISC) and Study Data Tabulation Model (SDTM)
- Ability to manage competing priorities and can work in a dynamic environment
- Comfortable writing and troubleshooting complex SQL queries that include PIVOT, Indexing, CTE’s, Subqueries, etc.
Additional Information Clinical Ink is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.
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