Clinical Research Assistant
- (3283924)
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
- 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- Those with a Minimum 1-year related experience will be considered for a Clinical Research Assistant II
McLean is an Affirmative Action Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.