Job Overview
Manage the entire study start-up process, encompassing site selection, regulatory submissions, contracting and budgeting, and site activation.
A strategic plan for start-up will be devised in collaboration with cross-functional leads, ensuring timely delivery of studies.
The selected sites and countries will be optimized to maximize successful study outcomes through a comprehensive site activation plan.
Proactive identification and communication of any issues impacting delivery are crucial for success.
Regular monitoring of progress against timelines will help address delays or risks promptly.
Oversight and coordination of each step in the start-up process are essential to meet activation goals.
Cross-functional collaboration and effective communication among all functions involved during the start-up period are vital.
Performance metrics will be tracked and reported, providing transparency and accountability.
Serving clients through client-facing calls, you will be the primary point of contact for start-up activities with internal teams and sponsors.
Key qualifications include a Bachelor's degree in Life Sciences, Nursing, or a related field (Master's preferred), minimum 3+ years of experience in clinical trial start-up, demonstrated leadership expertise, proven ability to manage multi-country start-up activities and cross-functional teams in a matrixed environment, excellent project management, communication, and problem-solving skills, and ability to handle multiple priorities in a fast-paced, deadline-driven environment.