Global Site Activation Manager
Core
Lead site activation activities across global clinical trials to drive study start-up success and accelerate patient enrolment.
Role type
Senior Site Activation Manager (Clinical Research)
Builds
Global clinical trial programs for pharmaceutical and biotechnology sponsors
Domain
Life Sciences / Clinical Research / Global Regulatory Affairs
Required skills
Site identification and feasibility, Regulatory submissions and ethics approvals, Contract negotiation, Protocol amendments, Risk management, Cross-functional stakeholder leadership, Global compliance strategy, Project timeline and budget management
Preferred skills
Experience with AI-enabled technologies, Innovation in clinical trial delivery, Mentoring colleagues
Technologies
AI-enabled technologies
Responsibilities
Lead site identification, feasibility, regulatory submissions, ethics approvals and site contracting; Develop and execute Site Activation Management Plans; Perform protocol amendments; Drive study start-up timelines and critical milestones; Manage regulatory strategies, approvals and essential study documentation; Negotiate contracts and regulatory documents while ensuring local and global compliance; Identify risks, resolve issues and implement mitigation plans; Monitor project metrics, budgets, timelines and performance indicators; Provide project updates, reports, presentations and operational insights; Support proposal development, bid defence activities and customer engagement; Mentoring colleagues and contributing to continuous improvement initiatives
