Clinical Research Coordinator

Phase I-IV clinical research site is seeking a full time CRC. Under the direction of the Principal Investigator, the coordinator will assist and conduct clinical research studies in adherence with study protocols.

This is an immediate hire; salary, quarterly bonuses, medical and health benefits including 401k, sick leave and PTO.

Specific responsibilities including but not limited to:

• Coordination of day to day aspects of study related procedures such as: scheduling visits and procedures
• Assessment of inclusion/exclusion criteria, preparation for research visits, performing study visits, documentation
• Collection, processing, and shipping of various specimens

Required skills:

• Ability to work effectively with minimal supervision
• 3-5 years previous clinical trials experience
• Excellent verbal and written communication skills and attention to detail required
• Basic computer skills