Sr. Research Program Coordinator

• Oversee patient recruitment, screening for eligibility, and enrollment of eligible subjects for participation in RAFT trial. Explain the protocol in detail to potential patients, referring providers and participating providers.
• Enter data into Secure Redcap database for RAFT patients delivered at Johns Hopkins Hospital.
• Be the lead coordinator for the Clinical Coordinating Center (CCC) of the RAFT trial and facilitate all communication to the RAFT Data Coordinating Center (DCC).
• Work closely with the DCC to coordinate site management.
• Preparation, maintenance, and revision of IRB applications, while maintaining continual regulatory compliance.
• Participate in weekly RAFT trial meeting with CCC and DCC.
• Coordinate monthly local PI, Neonatology and potentially other subspecialty ZOOM meetings between the 8 sites.
• Processing of patient samples and coordination with sending samples to biobank at All Children’s Hospital.
• Collaborate with North American Pediatric Renal Trial and Collaborative to ensure capture of all required long-term patient data including PedsQL surveys and transfer of data to DCC.
• Work closely with the lead PI to maintain study expenditure tracking and reporting milestones for financial invoicing.
• Act as a liaison for various studies with sponsors, study monitors, patients and their care providers; assist various monitors during study monitor visits and audits.
• Draft reports on study progress for the NIH.
• Participate in Data Safety Monitoring Board meetings to keep and circulate minutes
• Help maintain the RAFT website and clinicaltrials.gov
• Attend biannual conference for the North American Fetal Therapy Network to coordinate meetings between lead and local PIs at dedicated sessions.
• Participate in grant preparation to supplement study funds.
• Act as primary contact for JHH study participants, which may include scheduling, confirming appointments, and escorting/directing to various locations on/off campus.
• Other duties as assigned.

• Bachelor’s Degree in related field required.
• Three (3) years of related experiencerequired.
• Additional education may substitute for required experience, to the extent permitted by the JHU equivalency formula.

JHU Equivalency Formula:18 graduate degree credits (semester hours) may substitute for one year of experience.For jobs where equivalency is permitted, up to two years of non-related college course work may be applied towards the total minimum education/experience required for the respective job.

Preferred Qualifications:

• Clinical trial experience strongly preferred.