Clinical Research Assistant

Mass General Brigham•Belmont, MA

1d•$21 - $28•Onsite

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. The Pediatric Mood, Imaging, & NeuroDevelopment (PediMIND) Program at McLean’s Child Division seeks to advance what is known about the brain, behavior, and symptom mechanisms underlying child and adolescent mental health conditions, including suicide, non-suicidal self-injury, irritability, and bipolar disorder. Led by Daniel Dickstein MD who is also Chief of McLean’s Child Division and a Professor of Psychiatry at Harvard Medical School, the PediMIND Program is a multi-disciplinary team of psychiatrists, psychologists, and research assistants. We are recruiting a full-time clinical research assistant, whose duties include: • Working directly with child and adolescent research participants, helping conduct interviews, collect questionnaires, perform computer testing, assist MRI scanning, and help with data analysis and publication. • Provides assistance on clinical research studies as per study guidelines and protocols. • Recruits and evaluates potential study patients. Per protocol instruction, conducts telephone interviews and schedules patients for study visits or screenings. • Interacts with patients/subjects with regard to study, including participant education, procedural instruction, and follow up. Serves as a liaison between the participant and PediMIND research team. • Responsible for collecting data and maintaining participant information database for the study, including data input, data analysis, and running reports. Maintains participant records as part of record keeping function. • Responsible for sending various study information to study participants. • Answers phone calls and email inquiries about study protocol. Refers participants when appropriate to supervisor and research staff. • Monitors and sets up any needed equipment. • Maintains inventory and orders supplies when necessary. Prefer working knowledge of at least 2 of the following: (1) SPSS, (2) Excel, (3) MRI analysis software (e.g., AFNI, FSL, or SPM), (4) REDCap, or (5) basic unix (C-shell scripting) or python programming. • Some experience and interest in working with children, teens, or young adults preferred—whether in research, childcare, summer camp, team sports, or mentorship (big brothers/sisters). Summary Working under the supervision of a Senior Research Assistant, Manager or Principal Investigator and following established policies and procedures, provides assistance on clinical research studies. Supervisor available to handle unusual situations and regularly reviews progress of work.

Requirements

Bachelor's Degree required
Related experience 0-1 year
Careful attention to details.
Good organizational skills.
Ability to follow directions.
Good interpersonal and communication skills.
All employees must possess basic computer skills to use a variety of electronic or online systems for communication, clinical and administrative purposes.
Working knowledge of clinical research protocols.
Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
Works independently under close supervision.

Nice To Haves

Prefer working knowledge of at least 2 of the following: (1) SPSS, (2) Excel, (3) MRI analysis software (e.g., AFNI, FSL, or SPM), (4) REDCap, or (5) basic unix (C-shell scripting) or python programming.
Some experience and interest in working with children, teens, or young adults preferred—whether in research, childcare, summer camp, team sports, or mentorship (big brothers/sisters).

Responsibilities

Working directly with child and adolescent research participants, helping conduct interviews, collect questionnaires, perform computer testing, assist MRI scanning, and help with data analysis and publication.
Provides assistance on clinical research studies as per study guidelines and protocols.
Recruits and evaluates potential study patients. Per protocol instruction, conducts telephone interviews and schedules patients for study visits or screenings.
Interacts with patients/subjects with regard to study, including participant education, procedural instruction, and follow up. Serves as a liaison between the participant and PediMIND research team.
Responsible for collecting data and maintaining participant information database for the study, including data input, data analysis, and running reports. Maintains participant records as part of record keeping function.
Responsible for sending various study information to study participants.
Answers phone calls and email inquiries about study protocol. Refers participants when appropriate to supervisor and research staff.
Monitors and sets up any needed equipment.
Maintains inventory and orders supplies when necessary.
Collects and organizes patient data.
Maintains records and databases.
Uses software programs to generate graphs and reports.
Recruiting patients for clinical trials, conducts phone interviews and schedules patients for visits.
Obtains patient study data from medical records, physicians, etc.
Conducts library searches.
Performs administrative support duties as required.
Verifies accuracy of study forms.
Updates study forms per protocol.
Prepares data for analysis and data entry.
Assists with formal audits of data.
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 such as phlebotomy.
Assists with study regulatory submissions.
Writes consent forms.
Verifies subject inclusion/exclusion criteria.