Clinical Programmer evaluates, develops, and maintains clinical database and analyzes clinical data. Codes, tests and documents databases. Being a Clinical Programmer performs data validation and develops algorithms for data management, typically using SAS programming language. May require a bachelor's degree. Additionally, Clinical Programmer typically reports to a supervisor or manager. The Clinical Programmer works on projects/matters of limited complexity in a support role. Work is closely managed. To be a Clinical Programmer typically requires 0-2 years of related experience. (Copyright 2024 Salary.com)
About us
Comprehensive Clinical Research is a small business in West Palm Beach, FL. We are professional, agile and our goal is to help develop trials of today and cures of tomorrrow. .
Job Summary:
We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team. As a Clinical Research Coordinator, you will be responsible for assisting with the coordination and management of clinical research studies. This is a vital role in ensuring the successful execution of clinical trials and the advancement of medical research.
Responsibilities:
- Coordinate and manage all aspects of the clinical research site, clinical research studies, including patient care, enrollment, and follow-up
- Audit patient data, ensuring accuracy and adherence to protocols
- Perform patient monitoring
- Assist with the development and implementation of study protocols and procedures
- Collaborate with healthcare professionals to ensure compliance with medical standards and regulations
- Conduct documentation review to ensure completeness and accuracy
- Manage data entry and data management activities
- Assist with statistical analysis using appropriate software
- Maintain study records and ensure compliance with regulatory requirements
- Participate in study meetings and provide updates on study progress
Skills:
- Strong knowledge of medical terminology, systems, and standards
- Proficiency in data management and documentation review
- Familiarity with clinical research processes and regulations
- Experience in patient monitoring, including vital signs assessments
- Ability to collaborate effectively with healthcare professionals and study participants
- Excellent organizational skills and attention to detail
- Proficiency in statistical software for data analysis
We offer competitive compensation packages and opportunities for professional growth within our organization. If you are passionate about clinical research and making a difference in the field of medicine, we encourage you to apply.
Note: All positions at our organization are paid, including internship positions.
Job Type: Full-time
Benefits:
Healthcare setting:
Schedule:
Ability to Relocate:
Work Location: In person
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