What are the responsibilities and job description for the Clinical Research Registered Nurse position at The Heart House?
About Us:
The Heart House is a leading provider of cardiovascular care with a proud history spanning over 30 years. Our dedicated team of more than 30 board-certified physicians is committed to delivering comprehensive, compassionate, and innovative heart health services. Operating across six convenient locations in South Jersey, we serve a diverse community, offering a wide range of diagnostic, treatment, and preventive cardiac care. At The Heart House, our mission is to improve cardiovascular health and enhance the quality of life for our patients through excellence in clinical practice and patient-centered care.
The primary responsibility of the research nurse is to manage all aspects of conducting clinical trials. The research coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for the protocols, the research nurse/coordinator will act as liaison between the investigators, primary care providers, the institutional review board (IRB), and the sponsor. Along with the investigator, the coordinator will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the coordinator responsible for all data and source documentation, adverse experience reporting, and maintenance of complete regulatory files.
Job Responsibilities: Principal responsibilities or job duties
- 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 reporting form completion, and reporting of adverse drugs experiences).
- Maintenance of accurate and complete documentation, including but not limited to regulatory documents, signed information logs, subjects logs, and study-related communications.
- Organizational management of all aspects of the trial, including but not limited to timeliness in completing case report forms ( CRF’s), data entry, reporting adverse drug experiences (ADE’s), managing caseload 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 of subject compliance.
- Must be proficient in phlebotomy and IV insertion. Knowledge in Cardiology a plus. Must be able to work independently and willing to travel to other office locations if needed.
Pay: From $36.00 per hour
Benefits:
- 401(k) matching
- Dental insurance
- Employee assistance program
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Referral program
- Vision insurance
Work Location: In person
Salary : $36