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Coord,Clinical Research Ii - 100% Remote
Company | Talentify.io |
Address | United States |
Employment type | FULL_TIME |
Salary | |
Category | Staffing and Recruiting |
Expires | 2023-09-25 |
Posted at | 8 months ago |
Overview
- Comply with safety and infection control standards
- Schedule and conduct participant study visits, tests, interviews, and telephone follow-up calls
- Ensure adherence to study protocols and regulatory requirements
- Adhere to Good Clinical Practice guidelines and human subject protection practices
- Provide detailed written summaries from literature searches and related sources
- Monitor inventory of research-related supplies
- Document and collect data/samples for research procedures during participant study visits
- Contribute to the design, development, and documentation of study-related data and collection tools
- Obtain consent of research participants in accordance with IRB approved protocols and regulations, including HIPAA
- Assist with financial and operational aspects of grants and contracts, including clinical research billing review
- Present study status reports and contribute to data presentations and IRB processes
- Track and maintain study-related information in the data management system
- Ensure accuracy and completion of all regulatory documentation, including IRB and study data
- Conduct preliminary quality assurance reviews of study data
- Bachelor's degree in a scientific or health-related field, or equivalent experience
- 1-3 years of related experience
- Ability to travel to off-site locations
- May supervise research support staff
- Receives supervision from the Principal Investigator or designee
- Our mission at the DeafYES! Center for Deaf Empowerment and Recovery is to partner with the Deaf community to develop addiction and mental health resources tailored for Deaf signing people. Preference will be given to candidates who are Deaf or fluent in American Sign Language.
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