Clinical Research Coordinator

The Clinical Research Coordinator will manage all aspects of research studies, including developing and implementing SOPs, monitoring adherence to protocols, and designing IRB consent forms. They will also be responsible for data management, budget management, and communication with investigational sites and clinical consultants.

Requirements

• Bachelor's degree in biology, mathematics, computer science, natural sciences, or related areas
• Minimum of two years of related professional experience
• CITI certification preferred
• Phlebotomy training and/or certification required
• Ability to use Electronic Data Capture (EDC) systems and other software tools
• Strong IT skills, including MS Word and Excel
• Excellent oral and written English communication skills
• Ability to work independently and as part of a project team
• Good organizational and analytical/problem-solving skills with strong attention to detail

Benefits

• Generous Paid Time Off
• 401k Matching
• Retirement Plan