ppGeorgetown University comprises two unique campuses in the nation’s capital. With the Hilltop Campus located in the heart of the historic Georgetown neighborhood, and the Capitol Campus, just minutes from the U.S. Capitol and U.S. Supreme Court, Georgetown University offers rigorous academic programs, a global perspective, and unparalleled opportunities to engage with Washington, D.C. Our community is a close-knit group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world. /p h3Job Overview /h3 pServes as clinical research coordinator for phase I, II, and III oncology clinical trials conducted in the Clinical Research Management Office (CRMO) of Lombardi Comprehensive Cancer Center. /p h3Incumbent duties include, but are not limited to: /h3 ul liResponsible for overall coordination of assigned clinical trials throughout the trial lifecycle. /li liInterface with study participants and obtain and document informed consent according to protocol, institutional policies, and regulatory guidelines for minimal risk studies. /li liSchedule and coordinate study-related procedures and assessments while maintaining protocol integrity and patient safety and in accordance with Good Clinical Practice (GCP) guidelines. /li liAssist with triaging phone calls and proactive patient communication. /li liCoordinate collection of research specimens per protocol requirements. /li liSchedule in-service training for appropriate staff on assigned clinical trials. /li liRegularly update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials. /li liCollaborate with Data Manager(s) to assure documentation for the clinical trial is complete and accurate; assist with query resolution in a timely manner. /li liSchedule/facilitate sponsor meetings including PSV, SIV,



MV /li liDocument and report serious adverse events per protocol and institutional policy, with input from PI or senior member of clinical research team. /li liAct as a liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors. /li liOther duties as assigned. /li /ul h3Work Interactions /h3 ul liClinical Research Manager /li liDisease Group members: Principal Investigators, Physicians, Clinicians /li liClinical Research Management Office (CRMO) members: Clinical Research Nurses, Clinical Research Coordinators, Data Managers, Regulatory Coordinators, Laboratory Technicians /li liExternal department clinicians and staff: Infusion Nurses, Oncology Pharmacists, hospital staff /li liClinical trial sponsors, auditors, and study monitors /li /ul h3Requirements and Qualifications /h3 ul liBachelor’s Degree in a scientific or health related field required. /li liThree (3) to five (5) years of related experience in clinical research preferred. /li liStrong candidates exhibit:ul liAbility to work independently and function within a team. /li liStrong attention to detail. /li liReliable and able to prioritize competing responsibilities. /li /ul /li /ul h3Work Mode Designation /h3 pThis position has been designated as On-Campus. Please note that work mode designations are regularly reviewed in order to meet the evolving needs of the University. Such review may necessitate a change to a position’s mode of work designation. Complete details about Georgetown University’s mode of work designations for staff positions can be found on the Department of Human Resources website: .



/p h3Salary /h3 pb$61,000 ($29.33/hr) range $47,586 - $104,689 USD Annual /b /p h3Pay Range /h3 pThe projectedsalary or hourly pay range for this position which represents the full range of anticipated compensation is: b$20.16 - $31.30 /b /p h3Need Assistance: /h3 pIf you are a qualified individual with a disability and need a reasonable accommodations for any part of the application and hiring process, please visit the Office for Equal Opportunity Compliance website for general information about requesting accommodations, as well as information about requesting accommodations specifically for applicants. You also can also contact the Office for Equal Opportunity Compliance at or . /p h3Need some assistance with the application process? /h3 pPlease call . For more information about the suite of benefits, professional development and community involvement opportunities that make up Georgetown's commitment to its employees, please visit the Georgetown Works website . /p h3EEO Statement /h3 pGU is an Equal Opportunity Employer . All qualified applicants are encouraged to apply, and will receive consideration for employment without regard to age, citizenship, color, disability, family responsibilities, gender identity and expression, genetic information, marital status, matriculation, national origin, race, religion, personal appearance, political affiliation, sex, sexual orientation, veteran status, or any other characteristic protected by law . /p h3Benefits /h3 pGeorgetown University offers a comprehensive and competitive agevolazioni package that includes medical, dental, vision, disability and life insurance, retirement savings, tuition assistance, work-life balance benefits, employee discounts and an array of voluntary insurance options. You can learn more about benefits and eligibility on the Department of Human Resources website . /p /p #J-18808-Ljbffr

📌 Clinical Research Coordinator I (Prato)
🏢 Georgetown University
📍 Prato