Clinical Research Coordinator II

Mass General Brigham•Boston, MA

11d•Onsite

About The Position

The Clinical Research Coordinator II (CRC II) plays a central role in coordinating stroke clinical trials and supporting the administrative and operational needs of the New England Regional Coordination Center (NERCC) StrokeNet Clinical Trial Site. This position contributes to a national effort to design, launch, and manage high-impact clinical trials evaluating promising therapies. The incumbent will facilitate day-to-day coordination of assigned stroke trials, support network-wide administrative functions including SOPs and training materials, and ensure effective communication across participating sites. They will serve as a key liaison for investigators and collaborators, providing guidance on protocol, data, and regulatory matters. Responsibilities include generating reports, assisting with financial tracking, and working closely with site and network leadership to ensure milestones, timelines, and compliance requirements are 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

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.
Providing input into determining study subject suitability and recruitment strategy.
Performing data analysis, interpretation, QA/QC.
Assisting in completing reports and presentations.
Administering scores and evaluating study questionnaires.
Maintaining research data, patient files, regulatory binders, and study databases.
Performing data analysis and QA/QC checks and organizing and interpreting data.
Assisting with preparation for annual review and assisting PI in completing study reports and presentations.
May assist with training and orientation of new staff members.
Facilitate day-to-day coordination of assigned stroke trials.
Support network-wide administrative functions, including development and maintenance of SOPs, training materials, and shared resources.
Ensure effective communication systems across participating sites.
Serve as a key liaison for investigators and collaborators.
Provide guidance on protocol, data, and regulatory matters.
Generate reports for committees, funders, and regulatory bodies.
Assist with financial tracking and reconciliation.
Work closely with site and network leadership to ensure milestones, timelines, and compliance requirements are consistently met.