Institutional Research Director - Assistant assists in directing and overseeing institutional research for a university/college. Designs and leads institutional research studies evaluating the effectiveness of the organization's programs and policies. Being an Institutional Research Director - Assistant manages data collection and analysis and oversees the formulation of research reports. Requires a bachelor's degree. Additionally, Institutional Research Director - Assistant typically reports to Institutional Research Director. The Institutional Research Director - Assistant typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. To be an Institutional Research Director - Assistant typically requires 3+ years of managerial 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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