Clinical Research Coordinator

Mass General Brigham•Boston, MA

8d•Hybrid

About The Position

The Clinical Research Coordinator will work closely with Drs. Paola Pedrelli, Cristina Cusin, and Lauren Fisher across multiple studies. Current projects include studies evaluating digital biomarkers for the detection and monitoring of depression, as well as investigations of device-based and pharmacologic treatments for treatment-resistant depression. This position offers a rich and hands-on research experience, including participant interaction, data collection and management, and exposure to cutting-edge methodologies in clinical neuroscience and digital mental health. It is particularly well-suited for individuals interested in pursuing graduate training in psychology, public health, neuroscience, or medicine.

Requirements

Bachelor's degree
Strong writing skills
Strong organizational skills
Careful attention to details
Strong organizational skills
Ability to follow directions
Strong 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

Psychology, sociology, and premed majors are encouraged to apply
Prior research or clinical experience is strongly recommended
A strong interest in mental health research and working with individuals with depression is highly desirable

Responsibilities

Assist with recruitment and screening of participants for clinical trials
Verify subject eligibility based on inclusion/exclusion criteria
Provides basic explanation of study and in some cases obtains informed consent from subjects
Conduct study visits, including interviews and administration of assessments
Administers and scores questionnaires
Perform study procedures as required, which may include phlebotomy and EKG administration
Document participant visits and study procedures accurately
Obtains patient study data from medical records, physicians, etc.
Collect, enter, and organize study data from multiple sources (e.g., medical records, participant interviews)
Maintain accurate and up-to-date study databases
Verify accuracy and completeness of study forms and data entries
Update study documents and case report forms in accordance with study protocols
Maintain regulatory binders and ensure compliance with study protocols and institutional requirements
Assist with IRB submissions, amendments, and regulatory documentation
Support quality assurance and quality control (QA/QC) procedures
Assist with data analysis and generation of reports, tables, and figures
Conduct literature searches to support study development and manuscript preparation
Contribute to manuscript preparation and other scholarly outputs
Provide general administrative support for study operations
Coordinate communication among study team members and clinical staff