Clinical Research Assistant I Division of Alcohol, Drugs and Addiction
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. This position includes a great deal of patient contact and opportunities to learn research skills such as data collection, management, and analysis, as well as scientific writing. Working under the supervision of a Principal Investigator and following established policies and procedures, provides assistance on clinical research studies in a highly productive research group within the Division of Alcohol, Drugs, and Addiction at McLean Hospital under the direction of Roger D. Weiss, M.D. May be responsible for the following activities: recruiting and evaluating patients for studies; collecting and organizing patient data; scheduling patients for study visits; maintaining and updating data generated by the study, and assistance with preparing scientific presentations, posters, and writing papers for publication in scientific journals. 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.
Responsibilities
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
