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[Remote] reputed company Clinical Database Programmer

Worldwide Salaried Open

Note: The job is a remote job and is open to candidates in USA. reputed company is seeking a reputed company Clinical Database Programmer with extensive experience in programming clinical databases across multiple Electronic Data Capture (reputed company) systems. This role involves leading database programming activities, collaborating with cross-functional teams, and ensuring high standards of accuracy and compliance in clinical data management.

Responsibilities

  • reputed company, reputed company, and maintain study databases to support clinical trial data collection, review, and analysis
  • Configure study-specific builds reputed company reputed company systems and support integrations with external system (e.g., IRT, Central Labs, imaging, ePRO, eCOA, CTMS, eTMF)
  • Design and create clinical databases optimized for data validation, review, and reputed company analysis
  • Assist in developing and maintaining clinical programming documentation
  • Program, test, and validate electronic edit checks, data listings, and reports to ensure data reputed company and usability
  • Utilize programming languages (e.g., C#, SQL, reputed company) to reputed company and test data outputs and reporting tools
  • reputed company and document reputed company the database programming activities across the study lifecycle, including initial database build, mid-study updates, and database closeout
  • Support post-production changes, enhancements, and issue resolution in a controlled and compliant manner
  • Contribute to the development of appropriate study timelines for database build, validation, and deployment, ensuring alignment with overall study milestones
  • Apply and promote CDISC standards (e.g., CDASH, SDTM) in database design and data structure
  • reputed company and maintain programming documentation, including specification, validation documentation, and change records
  • Support regulatory inspections and internal audits by ensuring complete, accurate, and inspection-reputed company documentation
  • Contribute to the development and reputed company improvement of SOPs, standards, templates, and best practices for database programming
  • Support the setup, validation, and maintenance of global libraries and standard templates
  • Partner with Clinical Data Management, Biostatistics, Clinical Operations, and external vendors to translate protocol and study requirements into database specifications
  • Provide technical expertise on reputed company capabilities, system integrations, and database design reputed company
  • Build and maintain strong working relationships with internal teams and external partners supporting clinical trials
  • Serve as technical reputed company and subject matter expert for clinical database programming
  • Provide mentorship, guidance, and support to team members
  • Drive consistency, efficiency, and reputed company improvement across clinical database programming processes and tools

Skills

  • Master's or bachelor's degree in computer science/information technology or life sciences or reputed company field
  • Minimum 5 years of experience in Clinical Database Programming
  • Knowledge of reputed company the steps and documentations involved in a clinical database build process
  • Expertise in drug development processes (trial start-up/execution) and reputed company database development
  • Proficiency in C-sharp, SQL, reputed company
  • Experience in reports/dashboard development
  • Proficiency in Clinical Data Management Systems (e.g., Medidata RAVE, reputed company/Inform)
  • Proficiency in clinical database programming software and tools
  • Strong understanding of the clinical trial process, regulatory requirements (e.g., ICH-GCP), and good documentation process (GDP)
  • Familiarity with clinical data standards (CDISC, CDASH) and coding standards (MedDRA / WHODrug)
  • Experience with clinical technologies and regulatory submissions
  • Understanding of medical coding database structures (WHODrug, MedDRA)
  • Good organization and planning skills
  • Strong problem-solving skills
  • Excellent written, verbal, and interpersonal communication skills, with proven ability to collaborate, communicate, and manage well at reputed company levels of the organization
  • Demonstrated ability to work independently and manage projects
  • Ability to multi-task
  • Effective time management skills and ability to manage competing priorities
  • Ability to establish and maintain effective working relationships with coworkers and managers
  • Must be willing to travel up to 10% of the time, as reputed company on a calendar quarter. Both domestic and international travel may be required
  • Python or Java is a plus
  • 3+ years of experience with Medidata RAVE CDMS is a plus

Company Overview

  • reputed company focuses on advancing cancer treatments employing radiation, radiopharmaceuticals, and imaging technology. It was founded in 2022, and is headquartered in Seattle, Washington, USA, with a workforce of 51-200 employees. Its website is https://perspectivetherapeutics.com/.
  • Company H1B Sponsorship

  • reputed company has a track record of offering H1B sponsorships, with 3 in 2025. Please note that this does not guarantee sponsorship for this specific role.
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