Clinical Research Coordinator I

Mass General Brigham • Boston, MA

19h • Hybrid

About The Position

Mass General Brigham is a not-for-profit organization dedicated to patient care, research, teaching, and community service, striving to provide exceptional care and drive groundbreaking medical discoveries. The Center for Women’s Mental Health, a clinical and research program within the Department of Psychiatry at Massachusetts General Hospital, focuses on the evaluation and treatment of psychiatric disorders associated with female reproductive function. This includes consultations for psychiatric medications during pregnancy, treatment for postpartum mood and anxiety disorders, premenstrual syndrome, and menopause-related mood and anxiety symptoms, sleep disorders, and hot flashes. The research division examines a wide range of questions affecting women with psychiatric conditions, mirroring the center’s clinical expertise. Research coordinators are assigned 1-2 active research projects and are responsible for their implementation under the guidance of principal investigator(s) and supervision of the senior research coordinator. The team includes seven research coordinators, a research program manager, project manager, program coordinator, biostatistician, psychologist, and eleven psychiatrists, with three faculty members serving as principal investigators. Research coordinators collaborate closely with study principal investigators and meet weekly to review study progress and clinical cases. This is a full-time hourly hybrid position, with a 9:00-5:30 workday and a ½ hour unpaid lunch, located in the Simches Research Building (four days onsite, one remote).

Requirements

• Bachelor's Degree Science required
• Some relevant research project work
• 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

• 0-1 year preferred experience

Responsibilities

• Provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies
• Collecting and organizing patient data
• Scheduling patients for study visits
• Performing clinical tests such as phlebotomy, EKGs, etc.
• Maintaining and updating data generated by the study
• 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.

Benefits

• competitive base pay
• comprehensive benefits
• career advancement opportunities
• differentials
• premiums
• bonuses as applicable
• recognition programs designed to celebrate your contributions and support your professional growth

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees