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The Department of Surgery is seeking a Research Program Coordinator that will coordinate several cardiac surgeries related sponsored clinical studies in coordination with the cardiac surgery clinical trial nurses. This role is a critical component to the success for the cardiac surgery clinical trials program. The position will coordinate the implementation of research protocols as well as ongoing administrative processes related to these studies; screen and enroll patients and provide continued monitoring of these studies ensuring that all protocols are followed and status reporting, billing, and other regulatory components are performed correctly.

Specific Duties & Responsibilities

• Assist with preparation of IRB submissions.

• Coordinate all duties pertaining to opening new trials.

• Handle relevant patient biological specimens and follow protocol requirements Provide support and coordination for fellows and physicians during the planning phases of new trials. This would include protocol, consent and case report form development through enrollment, study completion and post study closure.

• Accountable for the overall administration and outcomes for trials requiring advanced-level knowledge and skills to manage a diverse portfolio of research responsibilities.

• Daily screening, recruitment, protocol adherence, schedule patient visits and assessments, as well as telephone follow up

• Blood sample processing to include obtaining specimens by phlebotomy and appropriate handling and labeling.

• Regular attendance at research meetings as well as providing updates on the study progress and issues related to the research.

• Prepare regulatory reports and maintain all regulatory binders for enrolling trials and trials in follow-up phase.

• Prepare and maintain individual participant study binders.

• Adhere to FDA regulatory compliance and regulations.

• Maintain appropriate correspondence with the IRB. Complete and submit IRB Change in Research Reports, including adverse events, protocol deviations and protocol amendments.

• Complete and submit annual IRB continuing review reports.

• Ensure quality, consistency, and accuracy in the conduct of research trials.

• Maintain the research data base including data entry

• Assist in clinical trial design.

• Assist with consenting study participants and documenting the consent process.

• Assist in data collection including patient contact for enrollment and follow-up.

• Prepare and submit annual continuing review reports

• Oversee record management for several research studies. Set up database, as well as processing systems and efficiencies for reporting purposes using Excel, Access, or similar systems

• Oversee budget development, as well as budget expenditures for study operations.

• Lead and participate in weekly research conferences.

• Conduct all study close out related procedures including IRB termination reports

Minimum Qualifications

• Bachelor's Degree in related discipline.

• Additional related experience may substitute for required education, to the extent permitted by the JHU equivalency formula.

Classified Title: Research Program Coordinator

Role/Level/Range: ACRO40/E/03/CD

Starting Salary Range: $17.00 - $30.00 HRLY ($50,000 targeted; Commensurate with experience)

Employee group: Full Time

Schedule: M-F

Exempt Status: Non-Exempt

Location: School of Medicine Campus

Department name: ​​​​​​​SOM Sur Cardiac Surgery

Personnel area: School of Medicine

Equal Opportunity Employer:

Johns Hopkins University is an equal opportunity employer and does not discriminate on the basis of race, color, gender, religion, age, sexual orientation, national or ethnic origin, disability, marital status, veteran status, or any other occupationally irrelevant criteria. The university promotes affirmative action for minorities, women, disabled persons, and veterans.