Clinical Research Monitoring (CRA)

The Clinical Research Associate is responsible for working directly with principal investigators to facilitate all aspects of research. Instrumental in study design, coordination, implementation, documentation and data management of research protocols to include budget preparation, monitoring and quarterly reports. Collaborates with hospital departments to coordinate research related activities.

May require travel to various sites.

CPR Training required and/or must be obtained within 45 days of hire.

Knowledge of research processes, procedures and regulations acquired through progressive experience in supporting or performing research.

3-5 years research experience preferred.

Must possess effective computer skills to include familiarity with Microsoft Excel, Access, and other standard software.

Exceptional interpersonal skills that display effective and professional customer service skills and interactions.

Ability to travel to various locations as required for performance of job role.

Patient care environment with exposure to environmental hazards including, but not limited to communicable diseases. Job will include normal office environment and travel to and through patient care areas. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, disability, gender identity, national origin, sexual orientation, veteran status, or any other status protected by federal, state, or local law.