Clinical Ethicist offers guidance to patients, their families, and professional staff on ethical, legal and policy issues and concerns stemming from clinical interactions between health care professionals and patients. Provides guidance to the institutional ethics committee pertaining to policy formulation and educational and case review activities. Being a Clinical Ethicist develops institutional policies concerning ethical issues such as "do-not-resuscitate" and "withdrawal of life-support". Requires a master's degree or doctorate related to health ethics. Additionally, Clinical Ethicist typically reports to a manager or head of a unit/department. To be a Clinical Ethicist typically requires 4 to 7 years of related experience. Contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. (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
Clear All
0 Clinical Ethicist jobs found in Boca Raton, FL area