Clinical Research Coordinator (Nephrology)

The Johns Hopkins University

Baltimore (MD)

On-site

USD 23,419 - 41,328

Full time

14 days+

Application generator

Stand out for this role — generate a tailored resume and cover letter in about a minute.

Get past ATS filters

Job summary

The Johns Hopkins University is seeking a Clinical Research Coordinator to support clinical trials and studies at the School of Medicine. This role focuses on coordinating protocol implementation, logistics, and study-related regulatory tasks to ensure compliant, efficient execution.

Responsibilities include participant consent, recruitment support, data entry, and collaboration with investigators and study personnel to advance research aims.

Qualifications

Bachelor's Degree in a related field required.
Experience in clinical research preferred or required per job listing.
Familiarity with IRB processes and study regulatory aspects.

Responsibilities

Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings.
Assist with IRB submissions and regulatory communications.
Explain study background to participants and coordinate recruitment and consenting processes.
Enter and organize data in study data collection systems and provide operational updates.

Skills

Clinical coordination

IRB submissions

Patient consent

Study logistics

Data entry

Education

Bachelor's Degree in related field

Tools

Electronic data capture (EDC) systems

Job description

We are seeking a Clinical Research Coordinator to support 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.

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 permitted by the JHU equivalency formula beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.

Preferred Qualifications