Site Optimization Specialist

Job Summary

A company is looking for a Site Optimization Specialist to support site leadership and corporate teams in the efficient start-up and delivery of multi-site clinical trials.

Key Responsibilities

• Promotes the company's image and clinical trial capabilities to enhance growth and profitability
• Facilitates communication and collaboration among stakeholders to ensure efficient delivery of trials
• Manages study start-up processes and monitors enrollment metrics to meet expected targets

Required Qualifications

• Bachelor's degree or equivalent experience in health sciences, business, project management, or related field
• Experience in clinical research roles such as Coordinator, Assistant, or Project Manager
• Familiarity with CTMS, EDC, and site operations
• Understanding of best practices, FDA regulations, and clinical protocols
• Ability to travel up to 5% as needed