Site Activation Manager (Global)

About the role

The Site Activation Manager (Global) leads the strategic, operational, and financial delivery of site activation activities across multiple studies and regions. This remote position ensures rapid site start‑up to support timely patient enrollment, covering site identification, regulatory submissions, and contracting.

Key responsibilities

• Provide strategic oversight and project management for global or multi‑regional site activation.
• Lead the end‑to‑end start‑up process from pre‑award through activation, ensuring compliance with ICH‑GCP and local regulations.
• Develop and execute a Site Activation Management Plan aligned with study strategy.
• Collaborate with internal teams, regional units, and external stakeholders to drive efficient study start‑up.
• Oversee regulatory submissions, approvals, contracts, and essential documentation.
• Identify risks, propose solutions, and support bid and business development activities.
• Mentor team members, drive continuous improvement, and maintain strong client relationships.

Required profile

• Bachelor’s degree in Life Sciences or a related field.
• Minimum 7 years of clinical research experience, including at least 3 years in a leadership role.
• Proven international project experience across multiple regions.
• Strong leadership, communication, and stakeholder‑management abilities.

Required skills

• ICH‑GCP compliance knowledge.
• Regulatory submission and approval processes.
• Project management expertise (planning, tracking, reporting).