Responsibilities
- Assists in enrolling participants for clinical study, explaining objectives, obtaining consent, recruiting and interviewing participants.
- Performs data collection and entry and tracks consent forms or other related materials.
- Prepares study materials and assists in developing databases and pretesting data collection input instruments. Generates basic recurring materials/reports.
- Assists in research project planning by monitoring established project timeline.
- Assists with developing and recommending study procedures.
- Assists with IRB submissions and supporting documentation.
- Assists in conducting literature reviews by searching library or online services as directed.
- May guide and train data entry staff on data entry processes.
- Can serve as a liaison between project and participants and/or outside groups.
Qualifications
Bachelor's degree in a related field; No experience is required. Except for qualifications established by law, additional related experience and formal education in which one has gained the knowledge, skills, and abilities required for full performance of the work of the job class may be substituted for the education or experience requirement on a year-for-year basis with 30 college credits being equivalent to one year of experience. Employees in this job class may be required to work with biohazardous or radio-labeled materials and may be required to successfully complete applicable safety training.
Job Info
- Job Category: Research
- Posting Date: 10/23/2026, 05:49 PM
- Apply Before: 10/30/2026, 05:00 AM
- Job Schedule: Full time
- Locations: 901 Harry S Truman Dr N, Largo, MD, 20774, US
- Expected Salary: $23.08/hour
- JobType: Contractual
