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Clinical Research Coordinator

Job

ASHA CLINICAL RESEARCH -MUNSTER,LLC

Hammond, IN (In Person)

Full-Time

Posted 1 week ago (Updated 1 week ago) • Actively hiring

Expires 6/15/2026

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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.
00 per hour
Benefits:
Health insurance Paid time off Application Question(s): we do not sponsor H1 or any other visas
Education:
Bachelor's (Required)
Experience:
Clinical research: 1 year (Required)
Work Location:
In person

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