The GW Medical Faculty Associates
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Research Nurse Coordinator (RN) - Surgery (Mon-Fri) OUTPATIENT
at The GW Medical Faculty Associates
Job Status: Full Time
Job Reference #: c1489503-18d5-4032-9c63-7a7f794ccf74
To participate in departmental and industry-sponsored research projects with primary functions devoted to study coordination. Working with study investigators, patients, and administrators in accordance with human subject’s research, Good Clinical Practice, and GWU contracts management guidelines.
Essential Duties and Responsibilities include the following. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Other duties may be assigned.
General Research responsibilities
Provide daily research support and administrative support for all assigned research projects and related activities
Assists in preparation of research grant and contract proposals and related budgets and justification documents.
Collects and provides as requested, all research grant and contract support materials including biographical sketches, CVs, non-disclosures, study surveys, 1572 forms, and other related technical documentation, necessary to conduct research.
Collects and presents, as requested, study budget information on a regular basis for the purpose of forecasting research expenditures and balances.
Conducts on-line research as needed to support ongoing and future research projects.
Assist in education and training of surgeons, residents and medical students in the field of research; conducts study in-services.
Attends Division of Surgical Research committee meetings. IRB Forum and other conferences as requested.
Sponsored Clinical Trials
· Prepare and participate in study approval visits, site initiation visits and sponsored travel to investigator meetings
Willing to travel 2-3 times a year to meetings
Knowledge of IRB, FDA and contract regulatory requirements
Conduct clinic visits with research participants – take history and health status information, perform venipuncture, vital signs, data collection (questionnaires and interviews) per protocol.
Recruit and consent participants for research studies
Complete case report forms per study sponsor guidelines
Experience with sponsored study data collections, reporting, auditing, etc.
Track, and report all participant adverse reactions
Prepare for and participate in study audits by IRB and sponsors
Enter participant data into study database, when necessary
Maintain study-specific records related to invoices, payments and related issues
Perform all procedures as necessary per study protocol