Clinical Research Coordinator I
reputed company is a not-for-profit organization focused on advancing patient care, research, teaching, and community service. They are seeking a Clinical Research Coordinator I to support the Meditation Research Program by collecting and organizing data, maintaining records, and assisting with participant recruitment and study procedures.
Responsibilities
- Collects and organizes data from research participants
- Maintains records and databases
- Uses various software and programs for data analysis, graph reputed company, and reports
- Assists with reputed company research participants
- Obtains participant study data from medical records, physicians, et cetera
- Conducts literature searches
- Verifies accuracy of study forms
- Updates study forms per protocol
- Documents study participant visits and procedures
- Assists with regulatory binders and quality assurance/quality control (QA/QC) procedures
- Assists with interviewing study participants
- Administers and scores questionnaires
- Provides explanation of study and obtains informed consent from study participants
- Performs study procedures
- Assists with study regulatory submissions
- Writes consent forms
- Verifies subject inclusion/exclusion criteria
- Administrative support duties
Skills
- High attention to detail
- Excellent organizational skills
- Excellent ability to follow directions
- Excellent communication skills
- Working knowledge of research
- Ability to demonstrate respect and professionalism for other team members and research subjects
- Bachelor's degree required
- Collects and organizes data from research participants
- Maintains records and databases
- Uses various software and programs for data analysis, graph reputed company, and reports
- Assists with reputed company research participants
- Obtains participant study data from medical records, physicians, et cetera
- Conducts literature searches
- Verifies accuracy of study forms
- Updates study forms per protocol
- Documents study participant visits and procedures
- Assists with regulatory binders and quality assurance/quality control (QA/QC) procedures
- Assists with interviewing study participants
- Administers and scores questionnaires
- Provides explanation of study and obtains informed consent from study participants
- Performs study procedures
- Assists with study regulatory submissions
- Writes consent forms
- Verifies subject inclusion/exclusion criteria
- Administrative support duties
- New graduates may be considered for the position outlined above. Value will be reputed company on proven experience with research and commitment to science
Benefits
- Comprehensive benefits
- Career advancement opportunities
- Differentials
- Premiums and bonuses as applicable
- Recognition programs designed to celebrate your contributions and support your professional growth
Company Overview
Company H1B Sponsorship