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- 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
- Assists with determining suitability of study subjects
- Maintains research data, patient files, regulatory binders and study databases
- Performs data analysis and QA/QC data checks
- Organizes and interprets data
- Has input into recruitment strategies
- Acts as study resource for patient and family
- Monitors and evaluates lab and procedure data
- Administers/scores/evaluates study questionnaires
- May contribute to protocol recommendations
- Assists with preparation for annual review
- Assists PI to prepare complete study reports & presentations
- Education; Bachelor's Degree
- Experience: Minimum 1-year related post bachelor's degree experience required
Clinical Research Assistant II - Belmont, United States - Partners Healthcare System
Description
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.
Principal Duties and Responsibilities