Clinical Research Coordinator

Mass General BrighamBoston, MA
$21 - $29Onsite

About The Position

The Clinical Research Coordinator I (CRC I) works under general supervision to support the team in enrolling eligible patients on oncology clinical trials. The CRC I will be responsible for scheduling all protocol mandated tests required to comply with institutional and federal regulations governing clinical research. This position involves direct patient contact.

Requirements

  • BA/BS degree required
  • None
  • Bachelor's Degree Related Field of Study required
  • Some relevant research project work 0-1 year preferred
  • Careful attention to detail and good organizational skills.
  • Ability to follow directions.
  • Good interpersonal and communication skills.
  • Computer literacy.
  • Working knowledge of clinical research protocols.
  • Ability to demonstrate respect and professionalism for subjects' rights and individual needs.

Nice To Haves

  • Some relevant research project work 0-1 year preferred

Responsibilities

  • Assist clinical team in screening potential patients for study participation
  • Schedule all protocol required tests and procedures
  • Coordinate patient appointments with physicians, nurses, and all test areas
  • Coordinate and schedule clinical safety laboratory specimen draws and ensure timely results are available to providers
  • Prepare pre-visit communication for providers to ensure required assessments are completed and documented
  • Maintain point of contact communication with enrolled patients and assist with front line questions regarding study participation
  • Develop protocol specific flow charts, intake sheets, and other tools to ensure protocol compliance and proper data acquisition
  • Coordinate, obtain, process, and ship protocol required tissue samples
  • Ensure collection and processing (e.g. spin/separate/freeze) of all required correlative research blood samples with the coordination of the MGH Sample Processing Lab (SPL)
  • Obtain vital signs and perform EKGs as required for individual studies
  • Administer quality of life assessments as required for individual studies
  • Scans in research documents and certifies these documents as copies

Benefits

  • comprehensive benefits
  • career advancement opportunities
  • differentials
  • premiums
  • bonuses
  • recognition programs
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