Clinical Research Coordinator (RN), Cancer Registry

University of Maryland Medical Center Baltimore WashingtonGlen Burnie, MD
27d$32 - $45Onsite

About The Position

Under general supervision of the principal investigator, plans and carries out key elements of a clinical research project. Is responsible for timely completion of deliverables to meet the needs of the study sponsor, principal investigator and department administration. All employees are responsible for extending the mission and values of University of Maryland, Baltimore Washington Medical Center by dedicating oneself to providing the highest quality healthcare services to the communities we serve. The University of Maryland Baltimore Washington Medical Center (UMBWMC) provides the highest quality health care services to the communities we serve. Our medical center is home to leading-edge technology, nationally recognized quality, personalized service and outstanding people. We have 285 licensed beds and we're home to 3,200 employees and over 800 physicians. Our expert physicians and experienced, compassionate staff are connected to medical practices in the local community as well as at University of Maryland Medical Center in downtown Baltimore. For patients, this means access to high-quality care and research discoveries aimed at improving Maryland's health. Our physicians and nursing staff specialize in emergency, acute, medical-surgical and critical care. In addition, our medical center is home to many Centers of Excellence, offering expert outpatient health care.

Requirements

  • Bachelor's degree in Nursing or Healthcare Administration or field of study related to the research of the clinic required or equivalent combination of education and experience. If RN, must be currently licensed in the state of Maryland.
  • Three (3) years related experience in a clinical research environment required.
  • May require training related to occupational safety and health, environmental compliance, shipping of hazardous materials and/or ionizing radiation.
  • Knowledge of key practices in the field as well as all relevant federal, state, local laws, regulations, and policies.
  • Skill in ethically communicating risks and benefits.
  • Skill in meeting multiple priorities and studies in various stages of development.
  • Ability to facilitate communications with the principal investigator, study sponsor, department administration, patients and their families.
  • Must have attention to detail and the ability to handle tasks in a timely manner.
  • Comprehensive knowledge of research principles and practices.
  • Skill in assurance of participant care.

Nice To Haves

  • Oncology experience preferred.
  • CPR license preferred.
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