Clinical Research Coordinator II

Responsible for coordinating all aspects of clinical trials with strict adherence to ICH, GCP, protocol, and company guidelines, regulations, and policies. Coordinates patient involvement, organizes research information, and monitors research data to maintain quality and compliance.

Requirements

• 2-3 years of experience in the medical field, preferred
• High school graduate or equivalent; Bachelors Degree, preferred
• CCRC certification preferred
• Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials
• Strong leadership and mentorship skills
• Effective communication skills

Benefits

• Health Insurance
• Dental
• Vision
• LTD
• STD
• Life Ins
• 401k