Clinical Research Coordinator

GENERAL SUMMARY

Under the supervision of the department manager and responsible research investigator(s), this position is responsible for the administration, coordination, database management and reporting requirements for designated approved clinical research. Reports to department leadership.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Assures and maintains professional standards for clinical practices in conducting clinical investigations.

Possesses and maintains an in-depth knowledge of federal regulations and guidance documents required for clinical trials and human subject protection, assuring compliance with protocol and regulatory requirements, and by collecting, recording and maintaining data and source documents.

Performs other duties as assigned.

LICENSES AND/OR CERTIFICATIONS

Current RN license required or other licensed medical provider working under MD supervision.

MINIMUM EDUCATION AND EXPERIENCE REQUIREMENTS

Bachelor’s degree required.

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

3-5 years clinical research experience preferred.

IRB familiarity preferred.

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

Ability to analyze and problem solve independently.

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.

WORKING CONDITIONS

Frequent exposure to communicable diseases, toxic substances, hazardous materials, radiation, radio nucleotides, medicinal preparations, body fluids and other conditions common to the healthcare environment.

PHYSICAL REQUIREMENTS

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