JOB SUMMARY
/ RESPONSIBILITIES :
- Provides assistance in one or more research-related activities : gathering information, project management, interacting with Investigators and coordinators, preparing protocols, collecting data and data entry, interviewing and scheduling patients, and collecting and analyzing data.
II. TYPICAL PHYSICAL DEMANDS :
Essential : seeing, hearing, and speaking.Frequent : standing, sitting, walking, stooping / bending, finger dexterity, repetitive arm / hand motions, frequent gripping of an object.Occasional : kneeling, crawling, climbing stairs, squatting, twisting body, lifting usual weight of 5 pounds up to 20 pounds, reaching above, at and below shoulder level, static gripping of an object.Operates computer, printer, telephone, typewriter, and copier.Additional Physical Demands for the Clinical Trials Office :
Operates : research equipment and medical / surgical devices.III. TYPICAL WORKING CONDITIONS :
Not substantially subjected to adverse environmental conditions.IV. MINIMUM QUALIFICATIONS :
A. EDUCATION / CERTIFICATION AND LICENSURE :
Bachelor's degree; or an Associate’s degree and two (2) years work experience in an administrative, clinical and / or academic research setting.B. EXPERIENCE :
Experience to demonstrate :o Knowledge and understanding of the research scientific process and protocol content.
o Knowledge of Microsoft Office applications (Outlook, Word, Excel).
o Ability to communicate effectively in English both orally and in writing.
o Ability to interpret and apply guidelines and follow procedures.
o Strong focus on accuracy with attention to details.
Assignment to the Regulatory Research Office :
Prior human subjects research experience preferred.