Global Site Activation Manager

About the role

As a member of the Global Study Leadership team, you will lead site activation activities across global clinical trials, partnering with sponsors, sites and cross‑functional teams to drive study start‑up success and accelerate patient enrolment worldwide.

Key responsibilities

• Lead site identification, feasibility assessments, regulatory submissions, ethics approvals and site contracting.
• Develop and execute Site Activation Management Plans aligned with study strategy and objectives.
• Drive study start‑up timelines, manage protocol amendments and ensure compliance with ICH‑GCP and local regulations.
• Negotiate contracts and regulatory documents while maintaining global and local compliance.
• Identify risks, resolve issues and implement mitigation plans, monitoring project metrics, budgets and performance indicators.

Required profile

• Bachelor’s degree in Life Sciences or related field.
• Experience in site activation, study start‑up, regulatory affairs or clinical operations.
• Strong knowledge of ICH‑GCP, clinical trial regulations and ethics processes.
• Proven ability to manage timelines, budgets, risks and cross‑functional stakeholders in a global environment.
• Excellent communication, negotiation and stakeholder management skills.