Fortrea
10,000+ employees
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
Healthcare • Biotechnology • Pharmaceuticals
Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.
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🔥 7 minutes ago
🗣️🇩🇪 German Required
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Fortrea
10,000+ employees
🏥 Healthcare
🧬 Biotechnology
💊 Pharmaceuticals
Healthcare • Biotechnology • Pharmaceuticals
Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.
📋 Description
• Assist with initial site outreach, including sending feasibility surveys and supporting collection of Confidentiality Agreements • Support preparation for Remote Pre-Study Visits (PSVs) and follow-up documentation such as trip reports and required materials • Coordinate basic administrative tasks related to contract and budget processes under guidance • Provide support for regulatory submissions and ethics committee documentation • Act as a point of contact for routine queries between sites and internal teams • Track site readiness and escalate blockers to senior team members • Maintain accurate records and assist with reporting of start-up metrics
🎯 Requirements
• Bachelor’s degree in life sciences or a related field (or equivalent experience) • Strong interest in clinical research and willingness to learn • Previous experience with study start-up and/or budget and contracts in clinical research • Basic understanding of ICH-GCP principles • Good organizational and communication skills • Fluency in German and English, written and spoken • Internship or exposure to clinical research or a healthcare environment preferred • Familiarity with MS Office tools • Knowledge of eTMF or CTMS is a plus
🏖️ Benefits
• Hybrid or remote work options with flexibility • Comprehensive onboarding and training programs to build your expertise • Access to Employee Resource Groups (ERGs) and wellness initiatives • Career development opportunities in a global organization • Inclusive culture that values diverse perspectives
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