Position: Clinical Research Coordinator
RN or EMT Required
ACLS and PALS Preferred
Night Shift Only - 4 10 hour or 3 12 hour shifts
Position Summary:
Responsible for assisting with the implementation of clinical trials, serving as a liaison between the investigative site and the Sponsor. Responsible for accurately documenting all information obtained throughout the clinical research process.
Qualifications:
1. Must be a high school graduate or have GED equivalency.
2. Must be capable of performing all clinical tasks relevant to licensure and/or training.
3. Must be able to clearly communicate verbally with patients.
4. Must have good interpersonal skills, demonstrated through interactions with patients, JBR staff, Sponsor representatives, etc.
5. Must be self-motivated and able to perform tasks independently.
6. Must reflect the professional image of the company, upholding the company vision in actions and demeanor.
Responsibilities:
1. Completes a company orientation program, prior to performing job responsibilities.
2. Reviews clinical protocols for assigned trials.
3. Develops, completes, and maintains source documents.
4. Recruits potential study subjects.
5. Screens, consents, and schedules subjects for study activities, according to protocol and as designated on the Delegation of Responsibility Log.
6. Administers or coordinates the administration of investigational medication and follows subjects through the study period, per protocol.
7. Conducts protocol required assessments.
8. Conducts the informed consent process, per JBR Standard Operating Procedures.
