Clinical Research Coordinator I/II

Site: 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.

 

The Center for Suicide Research and Prevention at MGB/Harvard is seeking applications for 1 full-time Clinical Research Coordinator (CRC) to coordinate and administer an NIMH-funded project (led by PI Drs. Jordan Smoller and Rebecca Fortgang) aimed at building and testing innovative new interventions to prevent suicidal behavior. The target population is adults leaving inpatient hospitalization or emergency department visit for suicide risk.

The Clinical Research Coordinator will be primarily responsible for recruitment and follow-up with participants in a clinical trial based out of the Mass General Brigham (MGB) emergency room and inpatient unit. Given the responsibilities of interacting with clinically severe/suicidal patients, hospital clinical staff, and supervising undergraduate and volunteer research assistants, strong interpersonal and organizational skills are essential. The role also requires a high level of initiative, autonomy, and followthrough; the successful candidate will be expected to manage responsibilities independently, proactively identify and address challenges, and seek out solutions and resources as needed. This position is particularly well-suited for anyone interested in pursuing graduate study in the fields of psychology, public health, or medicine.

Experience working with clinically severe/suicidal patients and strong interpersonal skills are strongly preferred. Writing, computer skills (e.g., proficiency with ecological momentary assessment and/or statistical software), and supervisory experience are highly desirable.

 

Job Summary

Summary
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; ensuring regulatory compliance; 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.

Does this position require Patient Care?
No

Essential Functions
-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.

 

Qualifications

EDUCATION

Bachelor's Degree Related Field of Study required

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

LICENSES & CREDENTIALS
Experience

• New graduates with some relevant course/project work or those without any prior research experience will be considered for a Clinical Research Coordinator I position.
• Those with a minimum of 1-2 years of directly related work experience will be considered for a Clinical Research Coordinator II position.

PRINCIPAL DUTIES & RESPONSIBILITIES

• Collects & organizes patient data
• Maintains records and databases
• Uses software programs to generate graphs and reports
• Recruits and enrolls patients for clinical trials
• Obtains patient study data from medical records, physicians, etc.
• Conducts library searches
• Verifies accuracy of study forms
• Updates study forms per protocol
• Documents patient visits and procedures
• Assists with regulatory binders and QA/QC procedures
• Assists with interviewing study subjects
• Administers and scores questionnaires
• Provides basic explanation of study and in some cases obtains informed consent from subjects
• Performs study procedures
• Assists with study regulatory submissions
• Assists with developing consent forms and study protocols
• Verifies subject inclusion/exclusion criteria
• Performs administrative support duties as req