Clinical Research Coordinator (Department of Dermatology)

The Johns Hopkins University; Baltimore (MD); On-site; USD 41,000 - 50,000; Full time

Job summary

The Johns Hopkins University is seeking a Clinical Research Coordinator to administratively coordinate protocol implementation for a clinical study. You will ensure efficient logistics, regulatory compliance, and data management, supporting the research team at the School of Medicine campus.

Responsibilities include coordinating study activities, assisting with IRB submissions, recruiting and consenting participants, and communicating with investigators and study staff.

Qualifications

• 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 or graduation equivalent.

Responsibilities

• Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings.
• Assist with preparation of IRB submissions and liaise with IRB on administrative matters.
• Explain study background and rationale to participants and obtain informed consent.
• Recruit participants using multiple strategies and scheduling of required activities and tests.
• Collaborate with nurses, coordinators, principal investigators and other staff to execute protocol-related activities.
• Oversee data collection, data entry, and maintenance of study records; monitor budget expenditures.

Education

Bachelor's degree in a related field

Job description

Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. We are seeking a Clinical Research Coordinator who will administratively coordinate clinical protocol implementation, typically for a single study. Will ensure efficient logistical implementation of the study activities and provide administrative support for research-related regulatory issues.

Specific Duties & Responsibilities

• Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings.
• Participate in clinical study start-up meetings.
• Assist research nurses, study coordinators, principal investigators, and other study personnel in executing protocol-related activities.
• Explain the study background and rationale for the research to potential and current participants
• Contribute to the development of recruitment strategies for participants for assigned study.
• Implement a variety of techniques for recruitment as appropriate, e.g., print and web-based advertisements, contact referring physicians, participate in community events, etc.
• Independently conduct the consenting process or ensure consent is obtained on appropriate participants.
• Schedule participants for required activities and provide any special instructions prior to upcoming tests/exams.
• Serve as liaison to study participants.
• Assist with setup of the data collection system and enter and organize data.
• Assist in coordinating study meetings.
• Participate in study meetings and provide updates on protocol implementation status and make recommendations on operational issues.
• Assist with the preparation of submissions to the Institutional Review Board (IRB)
• Liaison with IRB on administrative matters and facilitate communications with the PI.
• Conduct literature searches to provide background information.
• Obtain and maintain excellent operating knowledge of assigned clinical protocol, clinical equipment, and clinical computer systems.
• Oversee budget expenditures for study operations.
• Other duties as assigned.

Minimum Qualifications

• 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.

Preferred Qualifications

• Related undergraduate or work experience in human subjects research.

Classified Title: Clinical Research Coordinator

Role/Level/Range: ACRO37.5/03/CD

Starting Salary Range: $17.65 - $31.05 HRLY ($45,000 targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: M-F; 8:30am - 5:00pm

FLSA Status: Non-Exempt

Location: School of Medicine Campus

Department name: SOM Der Research Division

Personnel area: School of Medicine