Clinical Research Nurse

Job Summary A Clinical Research Nurse is a member of the research team who serves participants in clinical trials with direct patient care. This position is responsible for maintaining tight regulatory control over the health and safety of patients, as well as gathering and analyzing data for scientific study. Responsibilities Perform clinical functions such as phlebotomy and monitoring vital signs of study participants, educate family, and contribute to the care and evaluation of subjects, including determining preliminary inclusion/exclusion criteria. Manage multiple concurrent trials – screening, recruiting, and enrollment; perform patient/research participant scheduling; coordinate protocol‑related research procedures, study visits, and follow‑up; collect patient and research participant history; collect, maintain source documentation; perform data entry and query resolution; prepare IRB submissions; update required modifications; continuing reviews; and reportable events. Under the supervision of an investigator, conduct health assessments as medically necessary or required per protocol to assess or resolve adverse events, safety, and general health of study participants. Monitor study participants for adverse events and report any adverse events to the principal investigator and study coordinator, if applicable. Administer study interventions and treatments as directed by the principal investigator, if appropriate for scope of license. Prepare and monitor administration, usage, and documentation of investigational products and other required treatments in clinical trials. Perform and adhere to clinical functions commensurate with pertinent nursing license scope of practice (i.e., stay within state Board of Nursing scope for an LPN, RN, etc.). Maintain compliance with required hospital and unit‑specific training competencies and an active nursing license with the state Board of Nursing. Perform diagnostic tests and monitor participants' health through regular assessments. Observe, document, and report any changes in participant’s health status, and provide clinical care where necessary. Respond to emergencies and provide medical care as necessary and/or directed by a study investigator. Maintain frequent communication with research assistants and research coordinators regarding enrollment and tasks. Assist in the informed consent process of research subjects, if appropriate for scope of license. Support and advocate for the safety of research subjects. Collect, process, and ship laboratory specimens. Comply with Innovo, Clinic, and Sponsor policies, standard operating procedures (SOPs), and applicable regulatory requirements and guidelines. Provide training to new investigator/site staff members on study‑specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records. Perform all additional duties as assigned. Qualifications Current RN/LPN licensure in the state of employment. Associate Degree in Nursing from an accredited school of nursing. Certification in Clinical Research Coordination (CCRC) preferred. BLS required. Three years of prior experience in a health‑related clinic or research setting. Proficient in the use of Microsoft Office applications. Understanding of medical terminology. Strong organizational skills. Working knowledge of clinical trials. Effective time‑management skills with the ability to multi‑task and manage competing priorities with exceptional attention to detail. Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients. Practice a high level of integrity, honesty, and confidentiality. Benefits Competitive Salary Health Insurance Dental Insurance Disability Insurance Life Insurance Paid Time Off Vision Insurance Working Conditions This job operates in a professional and clinical environment with occasional visits to other Innovo Research partner sites and clinics. The role routinely uses standard office equipment such as computers, phones, and scanners. There is frequent exposure to communicable diseases, toxic substances, ionizing radiation, medicinal preparations, and other conditions common to a clinic environment. Varied activities include standing, walking, reaching, bending, and lifting. The position requires a full range of body motion, handling and lifting patients, manual and finger dexterity, and eye–hand coordination. It requires standing and walking for extensive periods, and occasionally lifting and carrying items weighing up to 50 pounds. Corrected vision and hearing to a normal range are required. Due to the nature of this position, employees are expected to work in person. This is an exempt position under federal and state wage and hour laws, meaning no overtime pay beyond the salary. Employees are expected to work 40 hours per week. Occasional evening and weekend work may be required as job duties demand. Equal Employment Opportunity Innovo Research is committed to the principle of equal employment opportunity for all employees and to providing a work environment free of discrimination and harassment. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV status, sexual orientation, gender identity and/or expression, marital or civil union status, military service, family medical history or genetic information, family or parental status, or any other status protected by law. Innovo will not tolerate discrimination or harassment based on any of these characteristics. Reasonable accommodations will be provided for qualified individuals with disabilities. Applicants must be authorized to work for any employer in the U.S. No sponsorship for employment visas is provided at this time. #J-18808-Ljbffr