Clinical Research Coordinator II-Oncology jobs in United States
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Johns Hopkins All Children's Hospital · 2 months ago

Clinical Research Coordinator II-Oncology

Johns Hopkins All Children's Hospital is a leading healthcare institution committed to serving the community. They are seeking a Clinical Research Coordinator II-Oncology who will be responsible for the overall coordination of assigned studies, ensuring protocol compliance and human subjects’ protection.

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H1B Sponsor Likelynote

Responsibilities

Serve as the primary coordinator on more-than-minimal-risk, high acuity, and/or complex studies. Serves as the liaison between study team, research cores/units/departments, ancillary hospital departments/services, sponsor, and IRB to ensure cross-communication and protocol compliance
Delegate tasks to the Clinical Research Coordinator I and Research Assistant in accordance with the delegation of authority log to ensure study is executed appropriately and efficiently
Coordinate the preparation and submission of regulatory documentation to the sponsor and Institutional Review Board (IRB) during all phases of study conduct including start-up, continuing reviews, changes in research, problem events, and closure to ensure human subjects protections and regulatory compliance
Operationalize the recruitment plan and obtain or coordinate the informed consent process to ensure the participant understands the information and volunteers to participate free of coercion
Coordinate and/or perform study visits/interventions/observations to ensure they are conducted according to protocol
Monitor participants for adverse events and study conduct for protocol deviations and events and report accordingly to Principal Investigator, sponsor, and IRB to ensure participant safety and protocol compliance, and participate in the Corrective and Preventative Action planning where applicable
Coordinate and perform data collection from various sources including medical records and enter data into research database to ensure accurate and timely data entry
Maintain organized and up-to-date research records including regulatory binders and participant records to ensure study documentation is audit-ready

Qualification

Clinical Research CoordinationClinical Practice (GCP)Regulatory ComplianceClinical Research Professional CertificationElectronic Data Capture (EDC)

Required

Bachelor's degree in science or health related field
3 years of prior clinical research coordination or nursing experience required
Certified as a Clinical Research Professional, or will obtain CCRP within 6 months of becoming eligible, but no later than 2 years after hire
Demonstrates knowledge and skills in accordance with Good Clinical Practice (GCP) guidelines, HIPAA, FDA regulations and other federally mandated guidelines
Must be comfortable working with patient populations
Computer competency in using Microsoft Office including Word, Excel, and Outlook

Preferred

prior experience with Electronic Data Capture (EDC) systems or databases

Benefits

Career growth and development
Employee and Dependent Tuition Assistance
Diverse and collaborative working environment
Affordable and comprehensive benefits package

Company

Johns Hopkins All Children's Hospital

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Johns Hopkins All Children's Hospital is a children's hospital located in St. Petersburg, Florida.

H1B Sponsorship

Johns Hopkins All Children's Hospital has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (2)
2024 (5)
2023 (1)
2022 (1)

Funding

Current Stage
Late Stage

Leadership Team

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Melissa Macogay
Vice President, Chief Nursing Officer
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Bethany Gregoire
Clincal Nurse Leader - CVOR
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Company data provided by crunchbase