RN / Registered Nurse- CRC / Clinical Research Coordinator - Neurology/Stroke - Sponsored Research at ProMedica Toledo, OH
Behavioral Health Market Context
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Job Description
largest board-certified medical staff, which is made up of more than 1,000 primary care and specialty physicians. Excellent customer service skills and the ability to work in a fast paced environment are a must. In addition, for 15 consecutive years, residents of Greater Toledo have named us the Consumer Choice Award winner in our market. In fact, we're the only hospital in northwest Ohio to receive this honor.
The CRC / Clinical Research Coordinator coordinates neurology/stroke-focused study protocols for the research department. Clinical trials involve enrolling patients in fast-paced, cutting-edge, acute care stroke and traumatic brain injury studies in collaboration with physician leaders in stroke, neurology and neurosurgery. Performs necessary patient procedures and data collection to ensure compliance with Federal and local research regulations. Maintains all documents in regulatory binder. Maintains patient-specific documentation and enters data into case report forms. Maintains through knowledge of all protocols. Ensures all documentation is complete.
• RN with valid license
• Prefer 5 years year's experience in coordinating clinical trials.
• Experience in neurology preferred
• Due to complex nature of tasks and extent of written and verbal communication, Science degree or degree in Health related field preferred
• Desire to work as part of a team with leaders in the field of Stroke Research
ProMedica is a mission-based, not-for-profit integrated healthcare organization headquartered in Toledo, Ohio. For more information, please visit
Qualified applicants will receive consideration for employmentwithout regard to race, color, national origin, ancestry, religion,sex/gender (including pregnancy),sexual orientation, gender identity or gender expression, age, physical or mental disability, military or protected veteran status, citizenship, familial or marital status, genetics, or any other legally protected category. In compliance with the Americans with Disabilities Act Amendment Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a job with ProMedica, please [email protected]
Equal Opportunity Employer/Drug-Free Workplace
The CRC / Clinical Research Coordinator coordinates neurology/stroke-focused study protocols for the research department. Clinical trials involve enrolling patients in fast-paced, cutting-edge, acute care stroke and traumatic brain injury studies in collaboration with physician leaders in stroke, neurology and neurosurgery. Performs necessary patient procedures and data collection to ensure compliance with Federal and local research regulations. Maintains all documents in regulatory binder. Maintains patient-specific documentation and enters data into case report forms. Maintains through knowledge of all protocols. Ensures all documentation is complete.
• RN with valid license
• Prefer 5 years year's experience in coordinating clinical trials.
• Experience in neurology preferred
• Due to complex nature of tasks and extent of written and verbal communication, Science degree or degree in Health related field preferred
• Desire to work as part of a team with leaders in the field of Stroke Research
ProMedica is a mission-based, not-for-profit integrated healthcare organization headquartered in Toledo, Ohio. For more information, please visit
Qualified applicants will receive consideration for employmentwithout regard to race, color, national origin, ancestry, religion,sex/gender (including pregnancy),sexual orientation, gender identity or gender expression, age, physical or mental disability, military or protected veteran status, citizenship, familial or marital status, genetics, or any other legally protected category. In compliance with the Americans with Disabilities Act Amendment Act (ADAAA), if you have a disability and would like to request an accommodation in order to apply for a job with ProMedica, please [email protected]
Equal Opportunity Employer/Drug-Free Workplace
Qualifications
- •Excellent customer service skills and the ability to work in a fast paced environment are a must
- •RN with valid license
- •Prefer 5 years year's experience in coordinating clinical trials
- •Desire to work as part of a team with leaders in the field of Stroke Research
Benefits
Responsibilities
- •Clinical trials involve enrolling patients in fast-paced, cutting-edge, acute care stroke and traumatic brain injury studies in collaboration with physician leaders in stroke, neurology and neurosurgery
- •Performs necessary patient procedures and data collection to ensure compliance with Federal and local research regulations
- •Maintains all documents in regulatory binder
- •Maintains patient-specific documentation and enters data into case report forms
- •Maintains through knowledge of all protocols
- •Ensures all documentation is complete
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