Clinical Research Coordinator I

reputed company is a not-for-profit organization reputed company 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 reputed company
• Conducts literature searches
• Verifies accuracy of study forms
• Updates study forms per protocol
• Documents study participant reputed company and procedures
• Assists with regulatory binders and reputed company assurance/reputed company 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 reputed company
• 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 reputed company
• Conducts literature searches
• Verifies accuracy of study forms
• Updates study forms per protocol
• Documents study participant reputed company and procedures
• Assists with regulatory binders and reputed company assurance/reputed company 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 reputed company
• 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 reputed company reputed company

reputed company

Company H1B Sponsorship