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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 vital role in the management of clinical trials, focusing on the administrative components essential for successful study execution.

Key Responsibilities

Trial Management: Oversee the clinical trial process, ensuring continuous communication with industry partners and study participants. Maintain accurate records, including patient files, regulatory documentation, and study databases.

Recruitment Strategies: Develop and implement effective strategies for participant recruitment, ensuring a diverse and representative sample.

Data Organization: Organize and analyze study data, providing insights and interpretations that support the research objectives.

Patient Interaction: Serve as a resource for patients and their families, guiding them through the consent process for various trials and biobanking initiatives.

Collaboration: Act as a liaison between the research clinic and external organizations, fostering partnerships that enhance research efforts.

Educational Outreach: Create and refine educational materials aimed at raising awareness about rare autoimmune diseases affecting the central nervous system, while supporting fundraising initiatives for the laboratory.

Qualifications

Education: A 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 necessary, with familiarity in autoimmune diseases of the central nervous system considered advantageous. Proficiency in a second language is a plus.

Skills: The ideal candidate will be a self-starter, capable of working independently as well as collaboratively. Strong communication and writing skills are essential, along with a high level of computer literacy.

Analytical Abilities: Candidates should possess strong analytical skills, with the capability to resolve technical issues and interpret data results effectively.

Work Environment: While much of the work can be conducted remotely, on-site presence will be required for patient consent and support activities.

Training: The role may involve orienting or training others as necessary.