The Clinical Research Coordinator ï¿½ Registered Nurse (CRC-RN) will assist the Principal Investigator in the conduct of all aspects of the clinical trial, including regulatory tasks, under the direct supervision of the Clinical Research Manager and affiliated Director. The CRC provides operational support in the management of patients accrued to multiple research protocols to assure subjectsï¿½ safety and regulatory compliance. The CRC is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, Standard Operating Procedures and all applicable regulations and guidelines and ensuring effective data flow associated with research protocols.
Responsible for the enrollment and protocol related care, treatment plan and schedule of events for the clinical trials portfolio, including the administration of investigational agents, ensuring compliance with the study protocol and participant safety. The clinical research nurse is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by Federal regulations. As the primary clinical resource for the protocols, the research nurse will coordinate and provide direct patient care, perform ongoing assessments, deliver patient education, and document in accordance with standards and regulatory guidelines pertaining to specified research patients enrolled onto clinical trials.
Bachelorï¿½s Degree in Nursing or related field.
Minimum or three (3) years of experience in clinical research to include healthcare compliance, research auditing, monitoring standards, or related experience.
Experience with medical record documentation review for accuracy, and compliance with all laws, rules, policies and procedures preferred.
Knowledge of GCP (Good Clinical Practice) and other FDA regulations pertinent to the conduct of clinical studies.
Knowledge of federal and state laws governing research preferred
Knowledge and understanding of both CPT and ICD-10 codes preferred.
Strong problem-solving, analytical skills and process management skills.
Planning, organizational and project management skills, interpersonal and oral/written communication skills.
Attention to detail and the ability to manage multiple priorities.
Ability to work without close supervision or guidance and to exercise independent judgment.
General computer/PC skills
Ability to adapt and effectively interface with all levels of employees in alignment with job responsibilities, policies and standards.
Registered Nurse ï¿½ licensed in the State of Florida
AHA Basic Life Support (BLS) certified.
SOCRA Certified Clinical Research Associate (CCRP) within 30 months of hire into the position.
Primary Location: Delray Beach, Florida
Facility: Delray Medical Center
Job Type: Full-time
Shift Type: Days
Employment practices will not be influenced or affected by an applicantâ��s or employeeâ��s race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.
Internal Number: 2005040935
About Delray Medical Center
Tenet Healthcare Corporation (NYSE: THC) is a diversified healthcare services company headquartered in Dallas with 112,000 employees. Through an expansive care network that includes United Surgical Partners International, we operate 65 hospitals and approximately 510 other healthcare facilities, including surgical hospitals, ambulatory surgery centers, urgent care and imaging centers and other care sites and clinics. We also operate Conifer Health Solutions, which provides revenue cycle management and value-based care services to hospitals, health systems, physician practices, employers and other clients. Across the Tenet enterprise, we are united by our mission to deliver quality, compassionate care in the communities we serve.