Oncology Research Nurse Coordinator for Clinical Trials

University of Maryland, Baltimore

Baltimore (MD)

On-site

USD 75,000 - 100,000

Full time

4 days ago
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Benefits offered by this job

Health insurance
Retirement plan
Paid time off
Professional development
Tuition remission
Flexible schedule / teleworking where

Job summary

The University of Maryland, Baltimore is seeking a full-time Nurse Coordinator for the Bone Marrow Transplant and Cellular Therapy team within the Greenebaum Comprehensive Cancer Center. The role interfaces with faculty and patients enrolled in clinical trials, coordinating regulatory communications and dose treatments per protocol.

The Nurse Coordinator supports regulatory processes, audits, and acts as a clinical consultant to staff, ensuring trial integrity and patient safety.

Qualifications

  • Bachelor's degree in Nursing or related field.
  • Five years as a Registered Nurse with at least one year in research.
  • Maryland RN license in good standing.
  • ACRP or SoCRA certification preferred.
  • Strong communication and data handling skills.

Responsibilities

  • Lead research studies and nurses involved in trials and care.
  • Oversee day-to-day clinical research operations and ensure protocol compliance.
  • Assist PI in obtaining consent and educate patients and families.
  • Coordinate IRB communication and prepare study reports for sponsors.
  • Maintain liaison with sponsors, departments, and regulatory bodies.

Skills

Communication
Nursing practice
Clinical research coordination
IRB communication
Education and training

Education

Bachelor's degree in Nursing

Tools

CTMS
EHR systems
IRB systems

Job description

The University of Maryland, Baltimore is seeking a full-time Nurse Coordinator for the Bone Marrow Transplant and Cellular Therapy team within the Greenebaum Comprehensive Cancer Center. The role interfaces with faculty and patients enrolled in clinical trials, coordinating regulatory communications and dose treatments per protocol.

The Nurse Coordinator supports regulatory processes, audits, and acts as a clinical consultant to staff, ensuring trial integrity and patient safety.

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