Clinical Research Coordinator
Job
ASHA CLINICAL RESEARCH -MUNSTER,LLC
Hammond, IN (In Person)
Full-Time
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Job Description
Clinical Research Coordinator Duties:
- Coordinate and oversee clinical research studies from start to finish
- Collect and analyze data, including vital signs,medical histories, meds and laboratory results
- Ensure compliance with study protocols and regulatory requirements, such as FDA regulations
- Manage participant recruitment and enrollment
- Schedule and conduct study visits, including blood sampling,processing and other procedures
- adherence to protocols
- Maintain accurate and complete study documentation
- Collaborate with investigators, sponsors, and other stakeholders to ensure smooth study operations
- computer skills must
- spirometry testing
Experience:
- Bachelor's degree in a related field (e.g., biology, nursing, or healthcare administration)
- Previous experience in clinical research coordination or related role preferred
- Knowledge of clinical trials management and FDA regulations
- Proficiency in clinical laboratory procedures, including phlebotomy
- Strong analytical skills for data collection and analysis
- Excellent organizational and time management abilities
- Ability to work independently as well as part of a team
Note:
This job description is intended to provide a general overview of the position. It is not an exhaustive list of all responsibilities, duties, skills, or qualifications required.Job Type:
Full-time Pay:
$24.00- $26.
Benefits:
Health insurance Paid time off Application Question(s): we do not sponsor H1 or any other visasEducation:
Bachelor's (Required)Experience:
Clinical research: 1 year (Required)Work Location:
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