Research Associate - Complex Family Planning (Full Time, 40, Day)

RESPONSIBILITIES

I. 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.

Equal Opportunity Employer/Disability/Vet