Rn - Clinical Research Coordinator (Varied Schedules Open) - Pa

The Clinical Research Coordinator Nurse is responsible for coordinating and managing clinical research studies, including patient recruitment, screening, and follow-up. They work closely with healthcare professionals and research teams to ensure that studies are conducted in compliance with regulatory requirements and ethical standards Physical Requirements: Ability to sit for long periods of time Manual dexterity to manipulate equipment and instruments Visual and auditory acuity to assess patient needs and monitor equipment Working Conditions: Clinical Research Coordinator Nurses work in research settings, including hospitals, clinics, and academic institutions. They may work long hours, including evenings and weekends, to accommodate study participant schedules. The work can be fast-paced and requires the ability to multitask and manage multiple study requirements. Culture Navitas Healthcare is passionate and hungry to secure and enhance our deliverables within every opportunity. With the expertise we have in staffing and consulting services, we are fully confident in providing temporary staff to perform any service; always being client-centric, solutions minded and putting your patients interest first. Recognized as a healthcare staffing leader, Navitas Healthcare is with you every step of the way. We excel in the business of human potential, and believe in its power to shape strategic, organizational, economic, societal change, and beyond. At Navitas Healthcare, we bring the perspective, understanding, and hands-on know-how to build the future as YOU see it. We help clients take care of patients. We help candidates find passionate work. We help give back to the communities. And we deliver it all with expectational customer service. Responsibilities Work with research teams to develop and implement study protocols Recruit and screen potential study participants, including obtaining informed consent Collect and manage study data, including maintaining accurate records and completing required documentation Coordinate study visits and procedures, including scheduling appointments and ensuring that study protocols are followed Communicate with study participants to provide education, answer questions, and ensure adherence to study requirements Work with healthcare providers to ensure that study procedures are completed safely and effectively Monitor study participants for adverse events and report any issues to the research team Ensure that studies are conducted in compliance with regulatory requirements and ethical standards Collaborate with other healthcare professionals and research teams to ensure the successful completion of studies Requirements Authorized to work in the US without sponsorship COVID-19 Vaccinated Minimum 6 months experience Equal Opportunity Employer Navitas Healthcare provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Requisition #clgv7o0m0eccp0ts71ef2x6wr