Georgetown irb login

Georgetown-MedStar IRB System

Georgetown-MedStar IRB System | Office of Research Oversight/Regulatory Affairs | Georgetown University

The system uses your either your Georgetown University or MedStar log-in. For full details on what account to use see “How to access the Georgetown-MedStar IRB …

How to log in to the Georgetown-MedStar IRB System

Institutional Review Board (IRB) | Office of Research Oversight/Regulatory Affairs | Georgetown University

The Georgetown University Institutional Review Board’s (IRB) primary role is to safeguard the rights and welfare of all human subjects who participate in …

The Georgetown University Institutional Review Board’s (IRB) primary role is to safeguard the rights and welfare of all human subjects who participate in research studies conducted by Georgetown. In compliance with Federal law and institutional policy, all research projects involving human subjects or human material must be reviewed and approved by the IRB. All biomedical social and behavioral research projects conducted by the faculty the staff and students of the University are subject to the Policies and Procedures of the Institutional Review Board.

Stacy Stone – IRB Analyst and IRB Systems Administrator

eRIC (Electronic IRB Submission System) | Office of Research Oversight/Regulatory Affairs | Georgetown University

eRIC (Electronic IRB Submission System) … Click Commerce IRB software to streamline Georgetown University’s Institutional Review Board (IRB) activities.

Georgetown University Medical Center – Myworkdayjobs.com

Using your web browser go to: https://gumedstarirb.georgetown.edu/IRB. Your username for the system is your MedStar network ID. Your password for the system …

IRB Analyst, Office of Human Subject Protections Georgetown …

Georgetown & MedStar Health eIRB Review Process | MedStar Health

The Human Research Protection Programs (IRBs) at both Georgetown University (GU) and MedStar Health … How to log-in to the Georgetown-MedStar IRB system.

The Human Research Protection Programs (IRBs) at both Georgetown University (GU) and MedStar Health (MedStar) use an electronic system to manage their respective Human Research Protection Programs and the IRB review process.

Senior IRB and Reliance Coordinator, Office of Human …

Georgetown University. Feb 2019 – Present4 years 1 month. Med-Dent Building. Share responsibility for the administration …

Act as an expert liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors. Provide guidance and training to …

Located in a historic neighborhood in the nation’s capital, Georgetown offers rigorous academic programs, a global perspective, exciting ways to take advantage of Washington, D.C., and a commitment to social justice. Our community is a tight knit group of remarkable individuals interested in intellectual inquiry and making a difference in the world. Requirements Clinical Research Coordinator – Lombardi Comprehensive Cancer Center – Georgetown University Medical Center Georgetown’s Lombardi Comprehensive Cancer Center (LCCC) seeks to prevent, treat and cure cancers by linking scientific discovery, expert and compassionate patient care, quality education and partnership with the community – guided by the principle of cura personalis – care for others. Job Overview The Clinical Research Coordinator supports clinical trials conducted at the Georgetown Medical Center and Lombardi Comprehensive Cancer Center in duties that include but are not limited to: Administer overall coordination of assigned clinical trials throughout the trial lifecycle Assist with the development and revision of research protocols and supporting documentation for submission to Georgetown University (GU) and MedStar Health (MedStar) Institutional Review Board and any external IRB, as needed Collaborate with investigators and other study team members by participating in the recruitment of study participants; and conduct participant screening and enrollment procedures and document eligibility data to support protocol compliance Interface with study participants and obtain and document informed consent according to study protocol, institutional policies, and regulatory bodies Coordinate or conduct study-related procedures and assessments while maintaining protocol integrity and participant safety and in accordance with Ethical Principles and Guidelines for the Commission for the Protection of Human Subjects of Biomedical and Behavioral Research Coordinate the collection of research specimens per protocol requirements Schedule/conduct/maintain required training for involvement with clinical trials Regularly update the Clinical Trials Management System (CTMS) with participant information and key dates to support responsible financial management of clinical trials, as appropriate Collaborate with Investigators and Data Manager(s) to assure documentation for the clinical trial is complete and accurate; and assist with query resolution in a timely manner Document study-related expenditures and collaborate with Financial Analyst(s) to assist study investigators in managing sponsored funds; and assist with expense queries in a timely manner Act as an expert liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors. Provide guidance and training to entry level coordinators Assist with other special projects, SOP development, and process improvement Perform all duties in accordance with applicable laws and regulations Adhere to Georgetown University Medical Center’s philosophies, policies, and SOPs Work in compliance with Human Subject Protection, participant confidentiality/HIPAA, and GCP Work Interactions Principal Investigators, Physicians, Clinicians External department clinicians and staff Clinical trial sponsors, auditors, and study monitors Qualifications Bachelor’s degree in a scientific or health related field – preference for Master’s degree 3 to 5 years of related experience Strong candidates exhibit ♦ Ability to work independently and function within a team ♦ Strong attention to detail ♦ Reliable and able to prioritize competing responsibilities ♦ Working knowledge of REDCap ♦ Database management. Work Mode: Hybrid. 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

IRB Analyst, Office of Human Subject Protections Georgetown University Medical Center – HigherEdJobs

This position is no longer an active posting on HigherEdJobs. IRB Analyst, Office of Human Subject Protections Georgetown University Medical Center. We require …

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Senior IRB and Reliance Coordinator, Office of Human Subject Protections – Georgetown University Medical Center at Georgetown University in Building D 2Nd Floor, Building D 2Nd Floor JR12510

Current Georgetown Employees: If you currently work at Georgetown University, please exit this website and login to GMS ( gms.georgetown.edu ) using your …

Senior IRB and Reliance Coordinator, Office of Human Subject Protections – Georgetown University Medical Center at Georgetown University in United States Of America – Building D 2Nd Floor – Building D 2Nd Floor. Located in a historic neighborhood in the nation’s capital, Georgetown offers rigorous academic programs, a global perspective, exciting ways to take advantage of Washington, D.C., and a commitment to social justice. Our community is a tight knit group of remarkable individuals interested in intellectual inquiry and making a difference in the world.RequirementsSenior IRB and Reliance Coordinator, Office of Human Subject Protections – Georgetown University Medical CenterJob Overview The IR JR12510