Clinical Research Coordinator (Endocrinology)

The Johns Hopkins University; Baltimore (MD); Hybrid; USD 37,000 - 65,000; Full time

Job summary

The Johns Hopkins University Division of Endocrinology is seeking a Clinical Research Coordinator to support clinical trials and studies focused on preventing and treating diseases. The role coordinates protocol implementation, ensures efficient study logistics, and provides regulatory support.

Responsibilities include coordinating study activities, assisting with IRB submissions, recruitment, consenting, data entry, and budget oversight.

Qualifications

• Bachelor's degree in a related field.
• Additional education may substitute for required experience per university policy.

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 staff in executing protocol-related activities.
• Explain the study background and rationale to participants.
• Contribute to recruitment strategies and implement recruitment techniques.
• Independently conduct the consenting process or ensure consent is obtained.
• Schedule participants and provide instructions for tests/exams.
• Serve as liaison to study participants.
• Assist with data collection and data organization.
• Coordinate study meetings and provide protocol updates.
• Assist with IRB submissions and communications with the PI.
• Maintain knowledge of assigned protocol, equipment, and systems.
• Oversee budget expenditures for study operations.

Education

Bachelor's Degree in a related field

Job description

The Division of Endocrinology is seeking a Clinical Research Coordinator, researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. The Clinical Research Coordinator administratively coordinates 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.

• To support clinically oriented research that targets the prevention and cure of type 1 diabetes.

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 ($45,000targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: Monday to Friday 8:30am - 5pm

FLSA Status: Non-Exempt

Location: Hybrid/School of Medicine Campus

Department name: SOM DOM Endocrinology

Personnel area: School of Medicine