Clinical Research Coordinator
About The Position
The Depression Clinical and Research Program, part of the Outpatient Psychiatry Division of Massachusetts General Hospital, is seeking a Clinical Research Coordinator. This program investigates the efficacy and safety of treatments for Major Depressive Disorder and aims to understand the causes and course of this disease. This position offers valuable experience for individuals interested in graduate studies in psychology, public health, or medicine. The role involves managing and coordinating clinical studies as a member of the research team, including screening patients, data entry and analysis, manuscript preparation, and performing clinical laboratory work such as phlebotomy and EKG administration. The coordinator will collaborate closely with physicians and psychologists to manage patient care throughout the studies.
Requirements
- Bachelor's degree
- Strong writing skills
- Strong organizational skills
- Careful attention to details
- 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
Nice To Haves
- Psychology, sociology, and premed majors are encouraged to apply
- Prior research or clinical experience is strongly recommended
Responsibilities
- Collects & organizes patient data
- Maintains records and databases
- Uses software programs to generate graphs and reports
- Assists with recruiting 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, which may include phlebotomy.
- Assists with study regulatory submissions
- Writes consent forms
- Verifies subject inclusion/exclusion criteria
- Performs administrative support duties as required
Benefits
- Comprehensive benefits
- Career advancement opportunities
- Differentials
- Premiums
- Bonuses as applicable
- Recognition programs
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
