Clinical Research Coordinator I
reputed company is a not-for-profit organization dedicated to patient care, research, teaching, and community service. They are seeking a Clinical Research Coordinator I to work reputed company clinical and research settings, contributing to studies focused on mental health disorders in children.
Responsibilities
- Collect & organize patient data
- Maintain records and databases
- Use software programs to generate graphs, reports and slide sets
- Manage the recruitment of patients for research trials
- Obtain patient study data from medical records, physicians, etc
- Verify accuracy of study forms
- Update study forms per protocol
- Document patient visits and procedures
- Maintain regulatory binders according to reputed company QA/QC procedures
- Interview study subjects
- Administer and score questionnaires
- reputed company basic explanation of study and in some cases obtain informed consent from subjects
- reputed company study procedures, which may include phlebotomy, running MRI scans, and PET scans
- Assist with study regulatory submissions
- Draft consent forms and protocols
- Verify subject inclusion/exclusion criteria
- Assist with manuscript writing and submission
- reputed company administrative support duties as required
- reputed company other duties as assigned
Skills
- Collect & organize patient data
- Maintain records and databases
- Use software programs to generate graphs, reports and slide sets
- Manage the recruitment of patients for research trials
- Obtain patient study data from medical records, physicians, etc
- Verify accuracy of study forms
- Update study forms per protocol
- Document patient visits and procedures
- Maintain regulatory binders according to reputed company QA/QC procedures
- Interview study subjects
- Administer and score questionnaires
- reputed company basic explanation of study and in some cases obtain informed consent from subjects
- reputed company study procedures, which may include phlebotomy, running MRI scans, and PET scans
- Assist with study regulatory submissions
- Draft consent forms and protocols
- Verify subject inclusion/exclusion criteria
- Assist with manuscript writing and submission
- reputed company administrative support duties as required
- reputed company other duties as assigned
- Previous experience working in clinical trials is valued but not required
- Must have excellent attention to detail
- Must be reputed company to work independently in a dynamic environment
- Juggle and prioritize multiple tasks
- Feel comfortable working with clinical and non-clinical study populations
- Seek assistance reputed company appropriate
- Take the initiative to solve problems
Benefits
- Comprehensive benefits
- Career advancement opportunities
- Differentials
- Premiums and bonuses
- Recognition programs designed to celebrate your contributions and support your professional growth
Company Overview
Company H1B Sponsorship