Clinical Research Assistant

Mass General BrighamBoston, MA
12h$18 - $22Onsite

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. The MGH Neuroendocrine Unit (Miller Group) is looking for an enthusiastic candidate for a clinical research coordinator position. The candidate will work with a dynamic team of physicians, nurse practitioners, and other clinical research coordinators. The prospective study coordinator will be supervised by the study clinician team and responsible for various aspects of clinical trial management and administrative tasks, including but not limited to scheduling and carrying out study visits, clinical trial protocol management, subject recruitment, data entry, and regulatory management. Projects mainly focus on the intersection between hormones and metabolic disease, including obesity, metabolic dysfunction-associated steatotic liver disease and women’s health. Job Summary Summary Encompasses a variety of clinical and administrative tasks and responsibilities which serve to facilitate the flow of patients through the clinic and to enhance the quality of care to patients. The emphasis is primarily administrative and placed on the ability to organize priorities, complete tasks, manage confidential patient information, schedule appointments, arrange diagnostic testing and referrals, and assist with insurance-related issues. Depending on interest, participation in research protocols may also be possible.

Requirements

  • High School Diploma or Equivalent required
  • Careful attention to details.
  • Good organizational skills.
  • Good communication skills.
  • Knowledge of clinical Research Protocols.

Nice To Haves

  • Knowledge of clinical Research Protocols 0-1 year preferred

Responsibilities

  • Collects and organizes patient data.
  • Maintains records and databases.
  • Uses software programs to generate graphs and reports.
  • Assists with recruiting patients for clinical trials.
  • Obtains patient study data from medical Records, Physicians, etc.
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