Clinical Research Coordinator, Pulmonary and Critical Care Medicine

Mass General BrighamBoston, MA
1d$20 - $29Onsite

About The Position

Site: The General Hospital Corporation Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Carry out a range of research activities in a large research project devoted to the investigation of lung cancer. Interaction with patients and families in Cancer Center and Thoracic Surgery requires good communication skills with patients, families and hospital staff, as well as the ability to remain focused in stressful situations. Job duties include screening eligible patients, recruiting participants, obtaining informed consent, collection of biological samples, and maintenance of clinical questionnaires, including extraction of data from medical records; data entry into databases. Excellent communication skills, dexterity, creativity, and independence required, in addition to meticulous attention to detail and organizational skills. Job Summary Job Profile Summary Summary Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; and maintaining and updating data generated by the study. Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification. Does this position require Patient Care? No

Requirements

  • Bachelor's Degree Related Field of Study required
  • 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

  • Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
  • Recruiting patients for clinical trials and conducting phone interviews.
  • Verifies the accuracy of study forms and updates them per protocol.
  • Prepares data for analysis and data entry.
  • Documents patient visits and procedures.
  • Assists with regulatory binders and QA/QC Procedures.
  • Assists with interviewing study subjects.
  • Assists with study regulator submissions.
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