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- Paterson, MD
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Clinical Research Nurse
Medix • Paterson, MD
Posted 15 days ago
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Clinical Research Nurse
Location: Rockville, MD
Pay: $70K - $80K
**THIS IS A GREAT OPPORTUNITY TO JOIN CLINICAL RESEARCH AND BE A PART OF GROUND BREAKING MEDICAL DISCOVERIES**
I understand that you can find an opportunity anywhere you go. You are needed and necessary however, companies have a big problem of not listening to YOUR needs and not valuing you as a person. I actually partner with HR teams to get your resume in front of the hiring manager and talk with them about your wants and needs. I will fight for you and make sure that you are heard and that you are VALUED most importantly.
Position Summary of Research Nurse:
Under general supervision of a physician and nurse is responsible for enlisting, maintaining and assuring protocol compliance for all patients on clinical trials. Collaborates with physician in determining eligibility of patients for clinical trials. Provides education to staff and patients. Ensures site research quality by practicing in compliance, Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations.
Job Responsibilities of a Research Nurse:
-Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol.
-Coordinates patient care in compliance with protocol requirements. May disburse investigational drug and provide patient teaching regarding administration. Maintains investigational drug accountability.
-In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
-Responsible for accurate and timely data collection, documentation, entry, and reporting. Schedules and participates in monitoring and auditing activities.
-Maintains regulatory documents in accordance with SOP and applicable regulations.
-Participates in required training and education programs. Responsible for education of clinic staff regarding clinical research.
-May collaborate with Research Site Leader in the study selection process.
-Additional responsibilities may include working directly with research bases and/or sponsors.
-Identify quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality.
-May be responsible for compiling and reporting protocol activity, accrual data, and research financial information to practice administration and physicians.
-May oversee the preparation of orders by physicians to assure that protocol compliance is maintained. Communicates with physician regarding study requirements, need for dose modification, and adverse event reporting.
-Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.