Clinical Research Coordinator (Oncology)

The Johns Hopkins University; Washington (District of Columbia); On-site; USD 23,694 - 41,741; Full time

Job summary

The Johns Hopkins University seeks a Clinical Research Coordinator to oversee clinical research activities and ensure study protocol compliance. Responsibilities include coordinating study activities, assisting with participant recruitment, and managing data collection. The ideal candidate will hold a Bachelor's Degree in a related field and be ready to support various research tasks.

This full-time position operates Monday to Friday and offers a starting salary between $17.20 and $30.30 hourly, depending on experience. Join a team dedicated to clinical research excellence at the School of Medicine.

Qualifications

• Bachelor's Degree in a related field.
• Education may substitute for experience.

Responsibilities

• Coordinate activities of a clinical research study.
• Assist research personnel with protocol-related activities.
• Implement recruitment strategies for participants.
• Conduct the consenting process for participants.
• Assist with data collection and organization.

Education

Bachelor's Degree in a related field

Additional education may substitute for required experience

Job description

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.

Classified Title: Clinical Research Coordinator

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

Starting Salary Range: $17.20 - $30.30 HRLY ($20.00-23.75/hour targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: Mon - Fri . 8:30a - 5p

FLSA Status: Non-Exempt

Location: District of Columbia

Department name: SOM Onc Sibley

Personnel area: School of Medicine