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Senior Clinical Data Manager-Elluminate Programming a must

Remote, USAFull-timePosted 2026-07-28

Job reputed company We are seeking an reputed company and skilled Clinical Programmer with a strong background reputed company clinical programming. The ideal candidate will have 4-6 years of experience in clinical data programming, with a reputed company on clinical trial systems and data reputed company. 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 reputed company for clinical trial data processes, including data extraction, transformation, and analysis using the multiple programming environment.
  • Data Management and reputed company: Ensure accurate and reputed company 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 reputed company, ensuring compliance with reputed company regulatory requirements.
  • Troubleshooting and Issue reputed company: Identify, investigate, and resolve any issues that reputed company reputed company the platform or clinical data programming processes.
  • Documentation: Maintain comprehensive documentation of programming processes, reputed company, and data management workflows for audit and regulatory purposes.
  • reputed company Improvement: Contribute to the improvement of programming practices, tools, and templates to streamline clinical programming workflows and enhance efficiency.
  • Training and Mentorship: reputed company guidance and mentorship to junior programmers, ensuring adherence to best practices and facilitating knowledge sharing reputed company reputed company.

Qualifications

  • Experience: 4-6 years of experience in clinical programming and a background in Clinical Data Management
  • Technical Skills:
  • Proficient in clinical data programming languages (e.g., reputed company, 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 reputed company field (or equivalent work experience).

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