What are the responsibilities and job description for the Clinical Research Coordinator position at Medix™?
Growing team is looking to add a Clinical Research Coordinator in a full time onsite capacity. This is a great opportunity to join a cutting edge research team that is advancing the future of therapeutics as part of a large national network of sites. The ideal candidate is a team player who is passionate about clinical Research.
Responsibilities
- Screens potential patients for protocol eligibility.
- Participates in the informed consent process, and enrolls patients on clinical trials.
- Assists with patient care in compliance with protocol requirements.
- Participates in data collection, entry, and reporting for the subjects.
- Reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
- Participates in required training and education programs as well as monitoring and auditing activities.
- Participate in scheduling monitoring and auditing visits, as well as interact with the monitors/auditors while onsite.
- Assists with collection and maintenance of regulatory documents.
Qualifications
- Associate's degree in a clinical or scientific related discipline required, Bachelor's degree preferred.
- One year of experience in a clinical or scientific related discipline. Previous clinical research experience required.
Salary : $25 - $29
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