Clinical Research Coordinator I

Mass General Brigham•Boston, MA

2d•$21 - $29•Hybrid

About The Position

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including 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.; and maintaining and updating data generated by the study. Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification.

Requirements

Bachelor's Degree Related Field of Study required
Some relevant research project work 0-1 year preferred
Advanced attention to detail and organizational skills.
Ability to follow directions and intellectual independence and initiative
Good interpersonal and communication skills.
Computer literacy, particularly excel, familiarity with statistical programming software
Working knowledge of clinical research protocols.
Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
Cover letter specific to the role in our Center, Resume, and Transcript (unofficial transcript is OK)
Applications that do not include all three components will NOT be considered.

Nice To Haves

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

Responsibilities

Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
Recruiting patients for clinical trials and conducting 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.
Participate in simulation model development and design
Execute simulation model runs to address critical policy research questions
Extract model projections and summarize findings in tables
Create publication-quality visualizations, dashboards, and decision-support tools that effectively communicate model output and analytical results
Collaborate with multidisciplinary domestic and international scientists to assess datasets, develop modeling methodologies, design research questions, and present model findings to policymakers, collaborators, and community partners
Assist in writing abstracts and designing posters for submission to research conferences
Present study results to project teams and external stakeholders
Assist with the preparation of Data Use Agreements, Institutional Review Board (IRB) applications, and related documents regarding the protection of human subjects
Perform systematic literature reviews and synthesize relevant data
Help prepare grant applications
Provide administrative support as needed, including organizing meetings and preparing slides for lectures and seminars