Research Associate - Research Regulatory Office; Temporary

RESPONSIBILITIES

Effective Date: 10/24

• Provides assistance in one or more research-related activities: gathering information, project management, interacting with Investigators and coordinators, preparing protocols, reviews Medicare Coverage Analysis (MCA) and budget, collecting data and data entry, interviewing and scheduling patients, and collecting and analyzing data.

• Finger dexterity, seeing, hearing, speaking.
• Frequent: standing, sitting, walking, stooping/bending, 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.

• Not substantially subjected to adverse environmental conditions.

• Bachelor's degree; or an Associate’s degree and two (2) years work experience in an administrative, clinical and/or academic research setting.

• Experience to demonstrate:
• Knowledge and understanding of the research scientific process and protocol content.
• Knowledge of Microsoft Office applications (Outlook, Word, Excel).
• Ability to communicate effectively in English both orally and in writing.
• Ability to interpret and apply guidelines and follow procedures.
• Strong focus on accuracy with attention to details.
• Assignment to the Regulatory Research Office:
  Prior human subjects research experience preferred.

Equal Opportunity Employer/Disability/Vet