
10,000+ employees
đ„ Healthcare
đ§Ź Biotechnology
đ Pharmaceuticals
Healthcare âą Biotechnology âą 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.
đ„ 14 hours ago
đ Germany, Austria â Remote
â° Full Time
đĄ Mid-level
đ Senior
âš Navigator
đ» Ghost score 10%
đŁïžđ©đȘ German Required
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10,000+ employees
đ„ Healthcare
đ§Ź Biotechnology
đ Pharmaceuticals
Healthcare âą Biotechnology âą 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.
âą Assist with initial site outreach, including sending feasibility surveys and supporting collection of Confidentiality Agreements âą Support preparation for Remote Pre-Study Visits (PSVs) and follow-up documentation such as trip reports and required materials âą Coordinate basic administrative tasks related to contract and budget processes under guidance âą Provide support for regulatory submissions and ethics committee documentation âą Act as a point of contact for routine queries between sites and internal teams âą Track site readiness and escalate blockers to senior team members âą Maintain accurate records and assist with reporting of start-up metrics
âą Bachelorâs degree in life sciences or a related field (or equivalent experience) âą Strong interest in clinical research and willingness to learn âą Previous experience with study-start up and/or budget and contracts in clinical research âą Basic understanding of ICH-GCP principles âą Good organizational and communication skills âą Fluency in German and English (written and spoken) âą Internship or exposure to clinical research or healthcare environment preferred âą Familiarity with MS Office tools preferred âą Knowledge of eTMF or CTMS is a plus
âą Hybrid or remote work options with flexibility âą Comprehensive onboarding and training programs to build your expertise âą Access to Employee Resource Groups (ERGs) and wellness initiatives âą Career development opportunities in a global organization âą Inclusive culture that values diverse perspectives
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