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Clinical Research Coordinator

2 months ago


San Antonio, United States Methodist Hospital Full time

Description IntroductionAre 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 Coordinator today with Methodist Hospital.BenefitsMethodist 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 wellbeing401(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 stockFamily 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 moreConsumer discounts through Abenity and Consumer DiscountsRetirement readiness, rollover assistance services and preferred banking partnershipsEducation assistance (tuition, student loan, certification support, dependent scholarships)Colleague recognition programTime 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 BenefitsNote: Eligibility for benefits may vary by location.Come join our team as a(an) Clinical Research Coordinator. We care for our community Just last year, HCA Healthcare and our colleagues donated $13.8 million dollars to charitable organizations. Apply TodayJob Summary and QualificationsOur teams are a committed, caring group of colleagues. Do you want to work as a Clinical Research Coordinator where your passion for creating positive patient interactions are valued? If you are dedicated to caring for the well-being of others, this could be your next opportunity. We want your knowledge and expertiseJob Summary and QualificationsYou will support enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirementsYou will be responsible for working with the principal investigator to meet or exceed study enrollment.You will review the study design and inclusion/exclusion criteria with physician and patientYou will ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements/complianceYou will ensure 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 dataYou will create study specific tools for source documentation when not provided by sponsorYou will collect, complete, and enter data into study specific case report forms or electronic data capture systemsYou will generate and track drug shipments, device shipments, and supplies as neededYou will report and follow up on serious adverse events as necessaryYou will implement study-specific communicationsYou will ensure timely adherence to protocol requirementsYou will be responsible for completion of all required documentation according to site works guidelinesYou will ensure timely and accurate data completionYou will maintain 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 communicationsYou will track and report adverse events, serious adverse events, protocol waivers, deviations, and violationsYou will communicate all protocol-related issues to appropriate study colleagues or managerYou will attend study specific on site meetings, investigator meetings, conference calls and monthly CRC meetings as required or asked to do soYou will apprise the principal investigator, Research Operations Director and Regional Site Manager of all study specific medical issues for guidanceYou will assist sponsor and US FDA audit teamsYou will review and respond to any monitoring and auditing findings and escalates issues defined by Regional Site ManagerWhat qualifications you will need: Knowledge of federal regulations, good clinical practices (GCP)Knowledge of medical and research terminologyComputer skills including use of clinical trial database, electronic data capture, and MS Word or ExcelExcellent Verbal and written communication skillsExcellent interpersonal skillsThe ability to communicate and work effectively with a diverse team of professionalsOrganizational and prioritizing capabilitiesThe ability to work independently in a fast pace environment with minimal supervision at off-site facilitiesAt least one year of experience as a Clinical Research CoordinatorBachelor’s Degree, work experience in lieu of Degree "The great hospitals will always put the patient and the patient's family first, and the really great institutions will provide care with warmth, compassion, and dignity for the individual."- Dr. Thomas Frist, Sr.HCA Healthcare Co-Founder If you are looking for an opportunity that provides satisfaction and personal growth, we encourage you to apply for our Clinical Research Coordinator opening. We promptly review all applications. Highly qualified candidates will be contacted for interviews. Unlock the possibilities and apply todayWe are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.