Inside Higher Ed
Clinical Research Coordinator II
role at Georgetown University Medical Center (as posted on Inside Higher Ed). Overview
The Clinical Research Coordinator II (CRCII) is the lead coordinator on multiple transplant (liver, kidney, pancreas, bowel) and GI clinical research studies, under the oversight of the Principal Investigator (PI) and direct supervision of the Clinical Trials Supervisor as well as the Research Director. The CRCII is responsible for the implementation of their assigned portfolio of studies, including regulatory submissions, data abstraction/entry/management, participant screening and enrollment, and study management. Given the role is an intermediate level position, the coordinator will manage moderate to high-level complexity studies. The role involves supporting the research on-call rotation amongst the research team to support transplant surgeries, enrollments, and the sample collection program. Work Interactions
The CRCII works under the direct supervision of the Clinical Trials Supervisor in partnership with the oversight of the Research Director and conducts the studies under direct oversight of the Principal Investigators (PIs). This individual will interact directly with patients, research participants, and their families. They work within the multidisciplinary team of the healthcare system and the university medical center, including the clinical research office, sponsored programs financial office, research development services, respective grants managers, and serve as primary point of contact with sponsors, CROs, and IRBs. Responsibilities
Lead coordination of CRC studies in transplant and GI portfolios, ensuring regulatory compliance and study integrity. Prepare and submit regulatory documents, maintain study files, and manage data entry/management. Screen and enroll participants, obtain informed consent, and coordinate study visits. Monitor study progress, timelines, and budgetary considerations; communicate with PI and sponsors as needed. Support on-call rotations to assist with transplant surgeries, enrollments, and sample collection programs. Qualifications
Bachelor's degree in a scientific or related field with at least 3 years CRCI or equivalent clinical research experience. An equivalent combination of education and experience may be substituted. Working knowledge of federal regulations and agencies including FDA and OHRP, and familiarity with ICH GCP. Strong organizational, critical thinking, and problem-solving skills. Working knowledge of clinical trials contracting and budgeting, including understanding of MCA and clinical trials billing compliance (industry and non-industry). Excellent interpersonal, verbal, and written communication skills. Strong proficiency in Microsoft, Google, data capture systems, electronic medical records, and other computer applications. Preferred
Experience with OnCore (Clinical Trials Management System). Certified clinical research professional (SoCRA or ACRP) preferred and required within one year of eligibility. Work Mode
The position has been designated as On-Campus. Work mode designations are regularly reviewed and may change to meet evolving needs. Details are available on Georgetown's mode of work designation. Pay Range
The projected salary range is $21.16 - $35.29 per hour, based on qualifications, experience, and university needs. How to Apply
To apply, visit the Georgetown Careers site: https://georgetown.wd1.myworkdayjobs.com/en-US/Georgetown_Admin_Careers/job/Medical-Center/Clinical-Research-Coordinator_JR23514-1 EEO Statement
Georgetown University is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, citizenship, color, disability, family responsibilities, gender identity and expression, genetic information, marital status, national origin, race, religion, sex, sexual orientation, veteran status, or any other characteristic protected by law. Benefits
Georgetown University offers a comprehensive and competitive benefits package, including medical, dental, vision, disability and life insurance, retirement savings, tuition assistance, work-life balance benefits, employee discounts, and voluntary insurance options. Details are available on the Department of Human Resources website.
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role at Georgetown University Medical Center (as posted on Inside Higher Ed). Overview
The Clinical Research Coordinator II (CRCII) is the lead coordinator on multiple transplant (liver, kidney, pancreas, bowel) and GI clinical research studies, under the oversight of the Principal Investigator (PI) and direct supervision of the Clinical Trials Supervisor as well as the Research Director. The CRCII is responsible for the implementation of their assigned portfolio of studies, including regulatory submissions, data abstraction/entry/management, participant screening and enrollment, and study management. Given the role is an intermediate level position, the coordinator will manage moderate to high-level complexity studies. The role involves supporting the research on-call rotation amongst the research team to support transplant surgeries, enrollments, and the sample collection program. Work Interactions
The CRCII works under the direct supervision of the Clinical Trials Supervisor in partnership with the oversight of the Research Director and conducts the studies under direct oversight of the Principal Investigators (PIs). This individual will interact directly with patients, research participants, and their families. They work within the multidisciplinary team of the healthcare system and the university medical center, including the clinical research office, sponsored programs financial office, research development services, respective grants managers, and serve as primary point of contact with sponsors, CROs, and IRBs. Responsibilities
Lead coordination of CRC studies in transplant and GI portfolios, ensuring regulatory compliance and study integrity. Prepare and submit regulatory documents, maintain study files, and manage data entry/management. Screen and enroll participants, obtain informed consent, and coordinate study visits. Monitor study progress, timelines, and budgetary considerations; communicate with PI and sponsors as needed. Support on-call rotations to assist with transplant surgeries, enrollments, and sample collection programs. Qualifications
Bachelor's degree in a scientific or related field with at least 3 years CRCI or equivalent clinical research experience. An equivalent combination of education and experience may be substituted. Working knowledge of federal regulations and agencies including FDA and OHRP, and familiarity with ICH GCP. Strong organizational, critical thinking, and problem-solving skills. Working knowledge of clinical trials contracting and budgeting, including understanding of MCA and clinical trials billing compliance (industry and non-industry). Excellent interpersonal, verbal, and written communication skills. Strong proficiency in Microsoft, Google, data capture systems, electronic medical records, and other computer applications. Preferred
Experience with OnCore (Clinical Trials Management System). Certified clinical research professional (SoCRA or ACRP) preferred and required within one year of eligibility. Work Mode
The position has been designated as On-Campus. Work mode designations are regularly reviewed and may change to meet evolving needs. Details are available on Georgetown's mode of work designation. Pay Range
The projected salary range is $21.16 - $35.29 per hour, based on qualifications, experience, and university needs. How to Apply
To apply, visit the Georgetown Careers site: https://georgetown.wd1.myworkdayjobs.com/en-US/Georgetown_Admin_Careers/job/Medical-Center/Clinical-Research-Coordinator_JR23514-1 EEO Statement
Georgetown University is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, citizenship, color, disability, family responsibilities, gender identity and expression, genetic information, marital status, national origin, race, religion, sex, sexual orientation, veteran status, or any other characteristic protected by law. Benefits
Georgetown University offers a comprehensive and competitive benefits package, including medical, dental, vision, disability and life insurance, retirement savings, tuition assistance, work-life balance benefits, employee discounts, and voluntary insurance options. Details are available on the Department of Human Resources website.
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