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The Rogosin Institute (RI) is a non-profit medical care and research organization affiliated with New York Presbyterian Health Hospital and Weill Cornell Medical College of Cornell University. Rogosin is one of the premier centers for the diagnosis and management of kidney disease in the country. The Institute also treats patients with diabetes, hypertension, lipid disorders and cancer and conducts research in these areas. We currently have an opportunity for a Research Nurse Practitioner who will manage all aspects of conducting clinical trials. As the primary resource for the protocols, the Research Nurse Practitioner will act as liaison between the investigators, primary care providers, the Institutional Review Board (IRB) and the sponsor. Along with the investigator will screen, enroll and follow study subjects, ensuring protocol histories and physical examinations as required by the protocol. In addition, is responsible for all data and source documentation, adverse experience reporting, and maintenance of complete regulatory files. May also assume a clinical role at one of the divisions of the Institute. |
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GENERAL RESPONSIBILITIES INCLUDE:
- Evaluation of volunteers and subjects including but not limited to performing histories and physical examinations
- Sound conduct of the clinical trial including but not limited to recruitment, screening, enrollment, and follow-up of eligible subjects according to protocol requirements (e.g. subject follow-up, case report form completion and reporting of adverse drug experiences)
- Maintenance 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
- 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), managing case load and managing study files
- Communication of all protocol-related issues/problems to the appropriate management staff, including but not limited to questions regarding the conduct of the clinical trial, concerns regarding possible ADE’s or subject compliance
GENERAL EDUCATION AND/OR EXPERIENCE INCLUDE:
Completion of training as a family or adult nurse practitioner. At least 1 year of clinical research experience as a nurse practitioner. Computer skills in word processing and spreadsheets.
CERTIFICATES, LICENSES, AND REGISTRATIONS:
Family or adult nurse practitioner license and registration in New York. Must have in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations.
SKILLS:
Clinical skills, language skills, reasoning ability and problem solving ability mandatory. Technical skills, organizational skills and computer skills necessary. Ability to communicate verbally and in writing in a professional manner with employees and institute contacts and ability to work on several different projects at one time.
We offer a competitive salary and superior benefits. For immediate consideration, please submit a cover letter and resume to: MYF9002@nyp.org . We are an Equal Opportunity Employer M/F/D/V.