Part-Time Senior Clinical Research Coordinator

Mass General BrighamBoston, MA
5dHybrid

About The Position

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. In this part-time Clinical Research Coordinator (CRC) role, you will coordinate a clinical randomized controlled trial (RCT) for our innovative parent-to-parent respite navigation program (RECHArge – Navigation REspite Resources for parents of CHildren with medical complexity to improve Access) to support access to care and services for children with medical complexity and their parent caregivers. You will play a pivotal role in supporting Dr. Amy Porter and her team to develop and manage the first clinical trial of a pediatric respite navigation program to support the vulnerable, under-resourced population of children with medical complexity and their families. Job Summary Summary Working independently and 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.; maintaining and updating data generated by the study. Additionally, provide input into determining study subject suitability, input into recruitment strategy, methodology design, statistical analyses, protocol design, and manuscript writing. Does this position require Patient Care? No

Requirements

  • Bachelor's Degree Science required
  • Related post-bachelor's degree research experience 1-2 years required
  • Ability to work more independently and as a team member.
  • Computer literacy, analytical skills, and ability to resolve technical problems.
  • Ability to interpret the acceptability of data results.
  • Working knowledge of data management programs.

Responsibilities

  • Independently determines the suitability of study subjects.
  • Develops and implements recruitment strategies.
  • Participates in the design of research methodology.
  • Plans, performs, and designs statistical analyses.
  • Recommends protocol changes, writes protocols, and contributes to manuscripts.
  • Independently performs specialized projects.
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