Marietta, GA, 30006, USA
19 hours ago
Clinical Research Nurse Coordinator
Description: The Clinical Research Nurse (RN) is a professional registered nurse, with research-specific knowledge and skills, who has general responsibility for managing clinical trials. This person ensures the integrity and quality of clinical trials are maintained and conducted in accordance with federal, state, and local regulations, Institutional Review Board (IRB) requirements, and health system policies and procedures. Utilizing the nursing process, the Clinical Research Nurse is primarily responsible for coordinating clinical trials in a manner that holds the protection of human subjects as the most important principle. Requirements: + 5+ years of inpatient nursing experience + 1+ years experience within clinical research + Active RN License in State of Georgia (or compact) in good-standing + BLS Certification Responsibilities: + Uses extensive knowledge of disease states to make complex decisions to provide patient-centered care. + Improves patient experience by maintaining close communications with physicians and coordinating subject progress from consent to end of study. + Ensures accurate research intervention (drug, device) by communication of dose modifications and protocol requirements to the physician investigator. + Administers protocol testing as required, after competencies are documented. Examples include vital signs, venipunctures, six-minute walk tests, and electrocardiograms. + Identifies and enrolls eligible subjects to clinical trials. + Maintains accurate records for patients enrolled on clinical trials. + Ensures accurate and timely reporting to sponsors, physician-investigators and regulatory entities. + Coordinates disbursement of and administers protocol provided drug therapy. + Provides patient education to ensure understanding of proper medication dosage, administration, and disease treatment. + Ensures that Investigation Product chain-of-custody practices are maintained. + Performs patient assessments to determine presence of adverse effects and reports appropriately. + Ensures that initial and ongoing protocol training is completed, including attending Investigator Meetings when required. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Confirm your E-mail: Send Email