Clinical Research Coordinator II

Mass General Brigham•Boston, MA

10d•$24 - $39•Onsite

About The Position

The Clinical Research Coordinator will play a central role in both coordinating individual stroke clinical trials and supporting the broader administrative and operational needs of the New England Regional Coordination Center (NERCC) StrokeNet Clinical Trial Site—a collaborative network to academic medical centers. As part of the NIH/NINDS StrokeNet infrastructure, this position contributes to a national effort to design, launch, and manage high‑impact clinical trials evaluating promising therapies from academic, foundation, and industry partners. The incumbent will facilitate day‑to‑day coordination of assigned stroke trials while also supporting network‑wide administrative functions, including development and maintenance of SOPs, training materials, and shared resources. They will ensure effective communication systems across participating sites, serve as a key liaison for investigators and collaborators, and provide guidance on protocol, data, and regulatory matters. Responsibilities include generating reports for committees, funders, and regulatory bodies; assisting with financial tracking and reconciliation; and working closely with site and network leadership to ensure milestones, timelines, and compliance requirements are consistently met.

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.

Nice To Haves

Can this role accept experience in lieu of a degree? Yes

Responsibilities

Assists with determining the suitability of study subjects and acts as a resource for patients and families.
Has input into recruitment strategies and may contribute to protocol recommendations.
Administers scores and evaluates study questionnaires.
Maintains research data, patient files, regulatory binders, and study databases.
Performs data analysis and QA/QC checks and organizes and interprets data.
Assists with preparation for annual review and assists PI in completing study reports and presentations.
May assist with training and orientation of new staff members.
Facilitates day-to-day coordination of assigned stroke trials.
Supports network-wide administrative functions, including development and maintenance of SOPs, training materials, and shared resources.
Ensures effective communication systems across participating sites.
Serves as a key liaison for investigators and collaborators.
Provides guidance on protocol, data, and regulatory matters.
Generates reports for committees, funders, and regulatory bodies.
Assists with financial tracking and reconciliation.
Works closely with site and network leadership to ensure milestones, timelines, and compliance requirements are consistently met.