Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)
The Research Coordinator /LPN m anages all aspects of conducting
clinical trials including acting as liaison between the investigators, primary
care providers, the institutional review board (IRB), and the sponsor/CRO.
Along with the investigator, the Research Coordinator/LPN will screen, enroll,
and follow study subjects, ensuring protocol compliance and close monitoring
while the subjects are on study. In addition, the Research Coordinator/LPN is
responsible for all data and source documentation, adverse experience
reporting, and maintenance of complete regulatory files. 1. Will participate and maintain a
culture within The Corvallis Clinic consistent with the content outlined in the
Service and Behavioral Standards Caregiver document. To this end, employee will
be expected to read, have familiarity, and embrace the principles contained
within. 2. Maintains of accurate and complete
documentation, including but not limited to regulatory documents, signed
informed consent forms, relevant IRB approvals, source documentation, drug
dispensing logs, subject logs, and study-related communications. 3. Sound conducts of the clinical trial,
including but not limited to recruitment, screening, enrollment, and follow-up
of eligible subjects according to protocol requirements. 4.
Organizational management of all aspects of the trial, including but not
limited to timeliness in completing case report forms (CRFs), data entry,
reporting adverse drug experiences (ADEs), timely communication with the IRB,
managing caseload and managing study files. 5.
Meets with potential research patients to explain
studies and assist the physician in the consent process. 6.
Coordinates resources for effective response in adverse
events and/or crisis situations. Consult
with study doctor to assess toxicities and adverse events, submit required
paperwork to study, regulatory and federal agencies as required. Assess and communicates all aspects of the
research patient’s protocol related care with investigator and study team. 7.
Responsible for patient teaching, advocacy and serve as
a resource for the research patient. 1.
Graduate of an accredited school of practical nursing
and current unencumbered LPN licensure in Oregon. 2.
Minimum of three (3) years practical nursing experience required. 3. Current Basic Life Support (BLS)
certification or ability to complete BLS certification within 90 days of hire
required. 4. 1.
Ability to work compatibly with physicians, patients,
and other staff. The work environment characteristics
described here are representative of those an employee encounters while
performing the essential functions of this job. The
noise level in the work environment is usually moderately quiet. Exposed to patient and environmental conditions, and
some unpleasant sights, smells, and contagious diseases. Summary:
Principal Responsibilities:
Education, Licensure and Experience:
Knowledge and Skills:
Work Environment: