Clinical Research Coordinator

GENERAL SUMMARY/ OVERVIEW STATEMENT:

The Valera Lab is looking for a per diem research assistant position. The RA will be assisting with projects focused on understanding the neurobiological and neuropsychological impact of repetitive traumatic brain injuries (TBIs) in women who have experienced intimate partner violence (IPV). Primary populations the RA would work with include women who have experienced physical IPV and women who have experienced IPV-related TBI. Neuropsychological and neurological testing are administered remotely, and the RA will be trained to run study visits over Zoom. We also employ multiple imaging modalities including diffusion tensor imaging (DTI) and structural and functional MRI. The RA will be trained to scan participants over a four month period. We also collect blood and hair from each participant, and therefore the RA may be asked to become certified in phlebotomy and learn how to process blood samples. Finally, the RA may choose to be involved in other ongoing research studies, including writing up and presenting results.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

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.

• Collects & organizes patient data
• Maintains records and databases
• Uses software programs to generate graphs and reports
• Assists with recruiting pariticipants and screening
• Conducts literature 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, which may include phlebotomy and MRI scanning.
• Assists with study regulatory submissions
• Verifies subject inclusion/exclusion criteria
• Performs administrative support duties as required

SKILLS/ABILITIES/COMPETENCIES REQUIRED:

• Careful attention to details
• Good organizational skills
• Ability to follow directions
• Good communication skills
• Computer literacy
• Working knowledge of clinical research protocols
• Ability to demonstrate respect and professionalism for subjects' rights and individual needs

EDUCATION:

• Bachelor's degree required in Psychology, Neuroscience, or a related field.

EXPERIENCE:

• New graduates with some relevant course/project work or those without any prior research experience will be considered for the Clinical Research Coordinator I position outlined above.

SUPERVISORY RESPONSIBILITY (if applicable):

• A Clinical Research Coordinator I does not have any supervisory responsibility.

Massachusetts General Hospital is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. Applications from protected veterans and individuals with disabilities are strongly encouraged.