Clinical Research Coordinator I
reputed company is a not-for-profit organization that supports patient care, research, teaching, and community service. The Clinical Research Coordinator I (CRC I) will contribute to research studies reputed company on mental health disorders in children, working under the supervision of the Program Director and in collaboration with other key personnel.
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 reputed company 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 reputed company
- Assist with manuscript writing and submission
- reputed company administrative support duties as required
- reputed company other duties as assigned
Skills
- Self-motivated, mature, and responsible
- Excellent organizational skills
- Excellent oral and written communication skills
- Excellent attention to detail
- Ability to work independently in a dynamic environment
- Ability to juggle and prioritize multiple tasks
- Comfortable working with clinical and non-clinical study populations
- Ability to reputed company assistance reputed company appropriate
- Initiative to solve problems
- Experience working in clinical trials (valued but not required)
- 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 reputed company 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 reputed company
- Assist with manuscript writing and submission
- reputed company administrative support duties as required
- reputed company other duties as assigned
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
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