Start-up & Regulatory Specialist IIShape the Future of Global Clinical TrialsJoin our dynamic team and lead the crucial start-up phase of impactful clinical trials, with opportunities for international exposure. You'll ensure projects are delivered on time, within budget, and to the highest quality standards, directly contributing to life-changing medical advancements.Your Impact:Drive the development and execution of efficient start-up processes.Spearhead site-related start-up activities, ensuring seamless initiation.Collaborate with clients and internal teams, presenting at key meetings.Manage timelines, budgets, and documentation with meticulous accuracy.Ensure regulatory compliance and adherence to the highest ethical standards.Your Expertise:Strong clinical research background (4+ years), including proven previous experience with study start-up projects.In-depth knowledge of ICH-GCP guidelines and international regulations (US FDA, MHRA).Excellent communication, leadership, and organizational abilities.Proven ability to manage multiple priorities and inspire teamwork in a virtual environment.Fluency in English and the local language.Ready to make a difference? Apply now!
#J-18808-Ljbffr