Clinical Research Coordinator - Cardiology

Scripps HealthSan Diego, CA
Onsite

About The Position

This is a full time, hourly position on the Cardiology research team on the campus of Scripps Memorial Hospital La Jolla. Join the Scripps Health team and work alongside passionate caregivers and provide patient-centered healthcare. Receive endless appreciation while you build a rewarding career with one of the most respected healthcare organizations nationwide. At Scripps Health, your ambition is empowered and your abilities are appreciated. Scripps Health is committed to providing the best possible patient care, and research is a critical part of that mission. In addition to bringing the latest treatments to our patients, the knowledge gained from these research studies advances the quality of care for people around the world. The Clinical Research Services team is responsible for feasibility and research coordination for all clinical trials across all specialties. Our research team is growing and we are excited to be part of progressive clinical trials that will contribute and assist our patients in living their best lives. The Clinical Research Coordinator will join our cardiology team.

Requirements

  • 2 years clinical trials or healthcare experience.
  • Advanced written, oral and interpersonal communication skills.
  • Strong prioritization, organizational, and problem solving skills.
  • Strong motivator/communicator in a compact clinical team working with aggressive timelines.
  • Strong computer skills with Microsoft Office software.
  • CCRP or CCRC required within 1 years of date of hire.
  • AHA BLS.

Nice To Haves

  • BS or BA.
  • 3 years clinical trials experience with an Associate's degree.
  • 4 years clinical trials experience as Medical Assistant or Lab technician.
  • Proficiency in medical terminology.

Responsibilities

  • Functioning as a liaison between the organization, investigators, and the research sponsors.
  • Responsibility for planning, implementation and oversight of a variety of clinical trials, maintains compliance with all applicable institutional, state and federal regulations in collaboration with investigator.
  • Performing independently as a project manager to coordinate all aspects of clinical research projects including administrative functions and clinical functions per scope of practice.
  • Recruiting, retaining, motivating and educating research patients in clinical trials, training other research personnel in research procedures, oversees research finances and tracking patient enrollment.
  • Working with other disciplines to execute trials, and acts as patient advocate to contribute to the overall research objectives of the program.

Benefits

  • Transitional and professional development programs to create a learning environment that enables you to thrive in your specific field as well as in your overall career.
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