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Mass General Brigham · 3 months ago

Clinical Research Coordinator NEUROLOGY KL

Boston-MA

Full-time

Onsite

New Grad, Entry Level

$19.76/hr - $28.44/hr

Mass General Brigham is a not-for-profit organization that supports patient care, research, teaching, and community service. The Clinical Research Coordinator will assist with clinical research studies, including recruiting and consenting patients, collecting data, and performing clinical tests while maintaining detailed logs and liaising with regulatory staff for clinical trials.

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Responsibilities

Assists research colleagues in the implementation, both internally and externally, of sponsored clinical research studies

Initiates and maintains contact with study participants

Responsible for screening applicants, ensuring they meet appropriate criteria, and making independent judgment as to the suitability of their participation

May be required to administer clinical tests such as smell tests, Montreal Cognitive Assessments, etc

There maybe opportunities to take history of patients, write up reports for attendings’ review, and shadow on a weekly basis

Working in concert with Principal Investigator and/or Research Manager, develops and implements patient recruitment strategies

Develops, organizes, and/or maintains study databases, including a registry of patients tracked by the division. Responsible for data validation and quality control

In conjunction with Research Manager/Principal Investigator, develops and implements new research protocols including design, data collection systems and institutional review board approval

Recommends changes to research protocols

Performs literature searches, as appropriate

Assists PI or Research Manager with preparation for presentation and written published articles; there are opportunities to communicate research to colleagues

Responsible for training and orienting new staff

Reviews proposals for compliance with sponsor and organizational guidelines; verify all sponsor requirements are met

Recruiting patients for clinical trials, conducts phone interviews

Verifies the accuracy of study forms and updates them per protocol

Prepares data for analysis and data entry

Documents patient visits and procedures

Assists with regulatory binders and QA/QC Procedures

Assists with interviewing study subjects

Assists with study regulator submissions

All other duties as assigned

Qualification

Clinical researchPatient recruitmentData managementPhlebotomyRegulatory complianceInterpersonal skillsIndependent work

Required

Candidates who are in the process of completing their bachelor's degree have a grace period of six months from their hire date (up to 1 year if starting per diem) to provide degree equivalency verification

Good interpersonal skills are required

Ability to work independently