Start-up & Regulatory Specialist II

Shape the Future of Global Clinical Trials

Join 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!

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