Clinical Research Nurse

Description Introduction Are you passionate about the patient experience? At HCA Healthcare, we are committed to caring for patients with purpose and integrity. We care like family Jump-start your career as a Clinical Research Nurse today with Chippenham Hospital. Benefits Chippenham Hospital offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include: + Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation. + Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more. + Free counseling services and resources for emotional, physical and financial wellbeing + 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service) + Employee Stock Purchase Plan with 10% off HCA Healthcare stock + Family support through fertility and family building benefits with Progyny and adoption assistance. + Referral services for child, elder and pet care, home and auto repair, event planning and more + Consumer discounts through Abenity and Consumer Discounts + Retirement readiness, rollover assistance services and preferred banking partnerships + Education assistance (tuition, student loan, certification support, dependent scholarships) + Colleague recognition program + Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence) + Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income. Learn more about Employee Benefits ( _Note: Eligibility for benefits may vary by location._ Come join our team as a Clinical Research Nurse. We care for our community Just last year, HCA Healthcare and our colleagues donated $13.8 million dollars to charitable organizations. Apply Today Job Summary and Qualifications The Research Nurse is responsible for coordinating multiple research protocols and serving as a liaison with local investigators, clinical staff, and research personnel. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a strong fundamental understanding of human subject research. Education & Experience: + This position requires an Associateu2019s Degree in Nursing; Bacheloru2019s Degree is preferred + RN license required + At least one year of experience in patient care setting required + Proficient in various electronic applications, Microsoft Office, EDC, CTMS required + Knowledge of basic medical terminology required Job Responsibilities: + Supports enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements + Responsible for working with the principal investigator to meet or exceed study enrollment. + Reviews the study design and inclusion/exclusion criteria with physician and patient + Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements/compliance + Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data + Ensures that adequate and accurate records are maintained for inspecting + Creates study specific tools for source documentation when not provided by sponsor + Collects, completes, and enters data into study specific case report forms or electronic data capture systems + Generates and tracks drug shipments, device shipments, and supplies as needed + Reports and follows up on serious adverse events as necessary + Implements study-specific communications + Ensures timely adherence to protocol requirements + Responsible for completion of all required documentation according to site works guidelines + Ensures timely and accurate data completion + Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, drug dispensing logs, device utilization logs, subject logs and study-related communications + Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations + Communicates all protocol-related issues to appropriate study colleagues or manager + Attends study specific on site meetings, investigator meetings, conference calls and monthly CRC meetings as required or asked to do so + Apprises principal investigator, Research Operations Director and Regional Site Manager of all study specific medical issues for guidance + Assists sponsor and US FDA audit teams + Reviews and responds to any monitoring and auditing findings and escalates issues defined by Regional Site Manager + Maintains patient confidentiality according to ethical and legal requirements + Assists in providing coverage for satellite clinic sites as necessary + Responsible for coverage after hours and on weekends as necessary You should have: + Knowledge of federal regulations, good clinical practices (GCP) + Knowledge of medical and research terminology + Computer skills including use of clinical trial database, electronic data capture, and MS Word or Excel + Excellent Verbal and written communication skills + Excellent interpersonal skills + The ability to communicate and work effectively with a diverse team of professionals + Organizational and prioritizing capabilities + The ability to work independently in a fast pace environment with minimal supervision at off-site facilities

Created: 2025-10-04