Senior Site Navigator

We are looking for a clinical operations professional to join our team as a Senior Site Navigator with a significant Start-Up experience, especially with contracts. This is an excellent role for someone looking to grow their career in clinical research within a global CRO environment.

Summary of Responsibilities:

• Assist with site contracts and budget negotiations
• Act as a primary point of contact for investigative sites during the start‑up phase
• Collaborate closely with CRAs, project teams, and study stakeholders to support study milestones
• Coordinate and track essential regulatory documents to ensure timely and compliant site activation
• Support site identification, feasibility, and start‑up activities, including site outreach, feasibility questionnaires, and confidentiality agreements
• Support ethics committee (IRB/IEC) submissions, renewals, and regulatory documentation in collaboration with internal teams
• Maintain accurate documentation in study systems and ensure the TMF is inspection‑ready

Qualifications (Minimum Required):

• University degree (life sciences preferred)
• Minimum 3 years’ experience in Clinical Operations or Start-Up
• Knowledge of ICH/GCP and clinical trial processes
• Fluent in English (written and spoken)
• Strong organizational skills, attention to detail, and willingness to learn
• Ability to manage multiple tasks in a structured and proactive way

Learn more about our EEO & Accommodations request here.