Clinical Research Coordinator

Intrastaff•Baltimore, MD

16h•Hybrid

About The Position

Johns Hopkins Intrastaff is the internal staffing agency for the Johns Hopkins Health System and partner hospitals, providing temporary support to a variety of the Johns Hopkins locations. Our employees are the strength of our service. Intrastaff is unique because it's one of the very few agencies where a person has the benefit of being a temporary employee and also feels like a member of a large organization. Working at Hopkins means joining a culturally diverse team that includes some of the best nurses, physicians and allied health professionals in the world. Directly or indirectly, you'll have exposure to cutting-edge technology and groundbreaking medical research. Location: Travel between JHH campus and Bayview campus Hours: 20 hours per week Pay range: $26-$28 per hour

Requirements

Bachelor's degree in a related field.
Additional education may substitute for required experience and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.
Work experience in human subjects preferred.

Responsibilities

Administratively coordinates clinical protocol implementation, typically for a single study.
Ensures efficient logistical implementation of the study activities and provides administrative support for research-related regulatory issues.
Coordinates all activities of a clinical research study to ensure adherence to protocol and validity of findings.
Participates in clinical study start-up meetings.
Assists research nurses, study coordinators, principal investigators, and other study personnel in executing protocol-related activities.
Explains the study background and rationale for the research to potential and current participants.
Contributes to the development of recruitment strategies for participants for assigned study.
Implements a variety of techniques for recruitment as appropriate, e.g., print and web-based advertisements, contact referring physicians, participate in community events, etc.
Independently conducts the consenting process or ensures consent is obtained on appropriate participants.
Schedules participants for required activities and provides any special instructions prior to upcoming tests/exams.
Serves as liaison to study participants.
Assists with setup of the data collection system and enters and organizes data.
Assists in coordinating study meetings.
Participates in study meetings and provides updates on protocol implementation status and makes recommendations on operational issues.
Assists with the preparation of submissions to the Institutional Review Board (IRB).
Liaises with IRB on administrative matters and facilitates communications with the PI.
Conducts literature searches to provide background information.
Obtains and maintains excellent operating knowledge of assigned clinical protocol, clinical equipment, and clinical computer systems.
Oversees budget expenditures for study operations.
Other duties as assigned.