Clinical Research Coordinator

Description

We are seeking a highly motivated Clinical Research Coordinator to join our team. The successful candidate will be responsible for coordinating and managing clinical research studies in compliance with regulatory requirements. The ideal candidate will have 2-11 years of experience in clinical research and excellent organizational and communication skills.

Responsibilities

• Coordinate and manage clinical research studies from start-up to close-out
• Ensure compliance with regulatory requirements and study protocols
• Maintain accurate and complete study documentation
• Manage study budgets and timelines
• Coordinate and communicate with study sponsors, investigators, and study team members

Skills and Qualifications

• Bachelor's degree in a related field (e.g. life sciences, nursing)
• 2-11 years of experience in clinical research coordination
• Excellent organizational and communication skills
• Experience with regulatory requirements (e.g. FDA, ICH, GCP)
• Experience with clinical trial management software (e.g. CTMS, EDC)
• Ability to work independently and as part of a team
• Strong attention to detail and problem-solving skills