Description

In this role, you will take charge of clinical research projects, ensuring they run smoothly and meet all standards. Your day-to-day responsibilities will involve leading teams, managing risks, and collaborating with global partners to deliver high-quality results.

Requirements

• •Minimum 5 years of experience in leading clinical trial operations within an SMO or CRO
• •Proven hands-on experience in managing clinical trial operations, including site start-up, contracting processes, and ongoing site management
• •Strong understanding of clinical trial logistics, investigational product handling, and supply management
• •Demonstrated experience in leading and developing teams of study coordinators or operational staff
• •Ability to independently manage and resolve complex, real-time operational issues
• •Excellent organizational, communication, and stakeholder management skills
• •Fluent in English
• •Language: English
• •Experience working in an international and cross-functional environment
• •Proactive, structured, and execution-focused leadership style

Tasks

• •Take end-to-end operational responsibility for clinical research projects
• •Ensure effective execution of clinical trials according to protocols and timelines
• •Oversee site qualification and support study start-up processes
• •Manage site contracting, activation, and coordination with stakeholders
• •Lead and support regional operational and business development teams
• •Act as a mentor and escalation point for coordinators facing challenges
• •Proactively manage risks and troubleshoot operational bottlenecks
• •Collaborate with internal global teams for project alignment and communication
• •Monitor operational KPIs and prepare progress reports
• •Implement corrective actions as needed
• •Represent Milestone One in discussions with sponsors and at industry meetings