Clinical Research Coordinator

We are seeking a Clinical Research Coordinator to execute feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level.

The successful candidate will prepare and manage site documentation, review and negotiate site documents and contracts with sites and sponsors, maintain, review, and report on site performance metrics, and serve as the primary point of contact for investigative sites.

Key responsibilities include:

• Serving as a Single Point of Contact (SPOC) to perform feasibility, site activation, and some maintenance activities in assigned studies for investigative sites
• Preparing site documents, reviewing for completeness and accuracy
• Informing team members of completion of regulatory, contractual, and other documents for individual sites
• Distributing completed documents to sites and internal project team members
• Updating and maintaining internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project-specific information
• Reviewing, tracking, and following up on the progress, approval, and execution of required documents

Requirements:

• Bachelor's degree in Life Sciences or a related field
• 1-3 years of clinical research or other relevant experience; or equivalent combination of education, training, and experience
• 3 years of experience in a healthcare environment or equivalent combination of education, training, and experience