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Clinical Trials Coordinator II

2 months ago

Boston, Massachusetts, United States Mass General Brigham Full time
Position Overview

The Clinical Research Coordinator II plays a pivotal role in managing the administrative components of clinical studies, including the informed consent process for participants and various outreach, educational, and advocacy initiatives for the Neuroimmunology Clinic and Research Laboratory.

Key Responsibilities
  • Oversee the execution of clinical trials, ensuring consistent communication with industry partners and study participants.
  • Maintain comprehensive records, including patient files, regulatory documentation, and study databases.
  • Develop and implement effective recruitment strategies to enhance participant enrollment.
  • Organize, analyze, and interpret research data to support clinical objectives.
  • Serve as a resource for patients and their families, providing guidance and support throughout the study process.
  • Facilitate communication between the Neuroimmunology Clinic and Research Laboratory and external organizations involved in related research.
  • Create and revise educational materials aimed at raising awareness about rare autoimmune disorders affecting the central nervous system.
  • Assist the development office in fundraising efforts to support laboratory initiatives.
  • Provide necessary support to both medical professionals and patients as required.
Qualifications

Education: Bachelor’s degree (BA or BS) is required; a Master’s degree (MA or MS) is preferred.

Experience: A minimum of 1-2 years of relevant experience is required; familiarity with autoimmune diseases of the central nervous system is advantageous. Proficiency in a second language is a plus.

Skills:

  • Self-motivated with the ability to work independently as well as collaboratively.
  • Exceptional communication and writing abilities.
  • High level of computer proficiency.
  • Strong analytical skills with the capability to troubleshoot technical issues.
  • Ability to assess the validity of data results.
  • Familiarity with data management software.

While much of the work can be conducted remotely, direct interaction with patients and support for medical staff will necessitate some on-site presence.

No specific requirements for orientation or training of others are indicated.