Senior Clinical Programmer – Elluminate

Job not on LinkedIn

🔥 0 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

🖥 Software Engineer

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 24%

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Clinical Outcomes Solutions

WebsiteLinkedInAll Job Openings

51 - 200 employees

💼 Consulting

🏥 Healthcare

🧬 Biotechnology

Consulting • Healthcare • Biotechnology

Clinical Outcomes Solutions is a global clinical outcomes consultancy that provides comprehensive support and services in all aspects of Clinical Outcome Assessment (COA) research. The company helps inform patient care by capturing the patient voice through innovative scientific methods. It guides organizations in navigating the complexities of clinical outcomes research by crafting strategies and solutions to capture accurate data. Trusted by pharmaceutical and biotechnology companies, the firm ensures regulatory compliance and optimized patient outcomes.

📋 Description

• Write and maintain code for clinical trial data processes, including data extraction, transformation, and analysis using the multiple programming environment • Ensure accurate and timely delivery of clinical trial data through data checks, validation, testing, and reconciliation • Design and implement clinical data flows with clinical data managers, statisticians, and other stakeholders • Ensure compliance with regulatory requirements • Identify, investigate, and resolve issues within the platform or clinical data programming processes • Maintain comprehensive documentation of programming processes, code, and data management workflows for audit and regulatory purposes • Improve programming practices, tools, and templates to streamline workflows and enhance efficiency • Provide guidance and mentorship to junior programmers

🎯 Requirements

• 4-6 years of experience in clinical programming • Proficient in clinical data programming languages, such as SAS, R, and SQL • Expertise in clinical programming platforms • Experience with clinical data workflows, data integration, and programming solutions • Strong knowledge of clinical trial data structures and data standards, including CDISC and SDTM • Knowledge of regulatory requirements, including FDA and EMEA • Excellent troubleshooting and problem-solving skills • Ability to work under pressure to meet deadlines • Strong communication skills • Ability to collaborate effectively with cross-functional teams and communicate technical concepts to non-technical stakeholders • Bachelor’s degree or higher in Computer Science, Life Sciences, Engineering, or related field, or equivalent work experience