Clinical Research Coordinator I (SPARC-XP Study )
About The Position
The General Hospital Corporation 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. Job Summary The SPARC-XP Study at Massachusetts General Hospital (MGH) is seeking a motivated, enthusiastic candidate to join our research group. SPARC-XP is led by Drs. Andrea Edlow, Roy Perlis, and Alysa Doyle, clinician-scientists and faculty in the MGH Center for Genomic Medicine who study different aspects of neurodevelopment. Dr. Edlow is an OB/GYN specializing in maternal-fetal medicine; Dr. Perlis is a psychiatrist and informatician; and Dr. Doyle is a child and adult psychologist. For other work in their labs, see https://edlowlab.org; https://perlislab.org; and https://thedoylelab.com. Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assigned to each position.
Requirements
- Bachelor's Degree Related Field of Study required
- Careful attention to detail and good organizational skills.
- Ability to follow directions.
- Good interpersonal and communication skills.
- Computer literacy.
- Working knowledge of clinical research protocols.
- Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
Nice To Haves
- Some relevant research project work 0-1 year preferred
Responsibilities
- Reviews proposals for compliance with sponsor and organizational guidelines; verify all sponsor requirements are met.
- Recruiting patients for clinical trials, conducts phone.
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
