Sponsor Dedicated Study Start Up Associate in Germany

We are looking for a Study Start-Up Specialist to join our sponsor-dedicated team. In this role, you will be at the forefront of clinical trial activation, ensuring regulatory approvals and site readiness for groundbreaking studies. This role is for upcoming future opportunities that may arise at Fortrea Key Responsibilities: Prepare, review, and submit essential documents to Ethics Committees (ECs) and Regulatory Authorities to ensure timely study approvals. Work closely with investigators and study teams to facilitate site selection, budget negotiations, and contract execution. Collect, review and track critical regulatory and start-up documents, ensuring compliance with ICH-GCP and sponsor requirements. Act as key point of contact between sponsor, sites and internal stakeholders to ensure seamless trial set-up. Identify and implement strategies to accelerate start-up timelines and improve efficiency. Required Qualifications: Bachelor\’s or Master\’s degree, preferably within Life Sciences or equivalent Minimum of one year of industry related experience in coordination of trial start-up activities and Health Authority / Ethic Committee submissions Familiarity with investigator start-up documents and contract/budgets negotiation process; previous interaction with operational project teams and investigative sites. Excellent computer systems\‘ proficiency Fluency in German and in English What we Offer: Work with an industry-leading sponsor and gain exposure to global clinical trials. Hybrid/remote options and a collaborative team culture Access to ongoing training programs and career advancement opportunities. Be part of a team that accelerates life-changing treatments to patients worldwide. Join us in shaping the future of clinical research and bringing life-changing treatments to patients faster. #LI-GQ1 #LI-Remote #LI-Hybrid Learn more about our EEO & Accommodations request here .