Clinical Research Coordinator I

Beth Israel Lahey HealthBoston, MA
13d$19 - $28Onsite

About The Position

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Responsible for screening patients for participation in clinical trials, enrolling patients onto these studies, monitoring protocol implementation, completing required forms and reporting results. Works closely with other clinical research staff. May be required to work varied shifts. This position is in the Emergency Department.

Requirements

  • Bachelor's degree required.
  • 0-1 years related work experience required.
  • Medical terminology.
  • Working knowledge of computer systems required, including web-based applications and some Microsoft Office applications, which may include Outlook, Word, Excel, PowerPoint or Access.

Responsibilities

  • Independently or in conjunction with other clinical research staff and/or research nurse, recruits and enrolls patients onto clinical trials according to study protocols. May assess patients' eligibility for inclusion in a particular protocol based on contracts with physicians and nurses and knowledge of the protocol.
  • Checks all eligibility and ineligibility criteria with the patients' medical record. Verifies information with clinical research nurse and/or principal investigator.
  • Discusses informed consent with patients. Interacts with patients prior to entering the study and throughout the entire treatment. Assists with scheduling appointments and follow up tests.
  • Learns protocol and monitors strict adherence to protocols by physicians, nurses and patients. Reviews protocol requirements with physicians, nurses and fellows. Identifies any problems with protocol compliance and notifies principal investigator and/or research nurse. Begins to learn how to independently resolve problems with protocol.
  • Extracts data on protocol patients from hospital records, outpatient charts and private physician office records in order to complete case report forms required by specific protocols. Enters data into computerized system.
  • May assist clinic staff in obtaining insurance approval for patient protocol participation and scheduling tests and arranging admissions or outpatient visits for patients.
  • Assists investigator with correspondence with IRB.
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