About the Role

Have you ever wanted to play a direct role in bringing life-changing therapies to patients who truly need them? At Precision Medicine Group, we are changing how clinical trials are run. As our footprint expands, we need a dedicated professional who speaks fluent Hungarian to step into our Regulatory and Start Up team. This is a fully remote position that you can perform from anywhere in the world. You will work alongside brilliant minds passionate about oncology and rare diseases while helping us navigate critical startup phases across assigned regions.

Overview

As a Regulatory and Start Up Specialist with us, you become a core pillar of our clinical trial operations. Your primary mission is making sure our trial sites reach activation readiness on time and without sacrificing quality. You will spot potential roadblocks before they happen and take action to keep projects moving forward smoothly. If you thrive in a collaborative environment and enjoy solving complex regulatory puzzles, this might just be your next great career move.

Key Responsibilities

Drive the timely and high quality delivery of site activation readiness within your assigned country and sites while proactively mitigating risks.
Prepare Clinical Trial Application Forms and assemble submission dossiers for initial filings, amendments, and notifications.
Coordinate closely with Competent Authorities, Ethics Committees, and local bodies to secure all necessary clinical trial authorizations.
Ensure every trial adheres strictly to international guidelines, local regulations, and internal company standards.

Requirements

Fluent in both Hungarian and English, with stellar written and verbal communication skills.
Demonstrated experience in clinical trial regulatory affairs and site startup activities.
A deep working knowledge of local and international regulatory frameworks governing clinical research.
Exceptional organizational skills combined with a sharp eye for detail.

What You'll Gain

The freedom to work completely remotely from anywhere across the globe.
A chance to work on groundbreaking oncology and rare disease trials that make a real difference.
Continuous professional development in a fast-growing global organization.
Supportive colleagues who value your expertise and unique perspective.