Manager

📋 Description

• Overseeing and directing the effective and timely initiation of clinical trial sites across various countries.

• Leading all start-up initiatives, ensuring adherence to regulatory standards, and collaborating with cross-functional teams to achieve study timelines and meet client expectations.

• Managing the entire study start-up process, which includes site selection, regulatory submissions, site contracting, budgeting, and site activation.

• Defining start-up strategies and timelines in partnership with the Project Manager and cross-functional leaders.

• Preparing and maintaining a comprehensive site activation plan.

• Proactively identifying and communicating issues that may impact delivery, along with proposing solutions.

• Monitoring progress against timelines and proactively addressing any delays or risks.

• Acting as the primary liaison among all functions involved during the start-up phase.

• Tracking and reporting on start-up performance metrics.

⛳️ Requirements

• Bachelor’s degree in Life Sciences, Nursing, or a related field (Master’s degree preferred).

• A minimum of 3+ years of experience in clinical trial start-up, demonstrating leadership capabilities.

• Proven track record of managing multi-country start-up activities and leading cross-functional teams in a matrixed environment.

• Excellent project management, communication, and problem-solving abilities.

• Capacity to manage multiple priorities in a dynamic, deadline-oriented setting.

🏝️ Benefits

• Permanent full-time position.

• Flexible schedule.

• Vacation.

• Home-based position.

• Ongoing learning and development.