As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in 100 countries, Fortrea is transforming drug and device development for partners and patients across the globe. Are you a dynamic leader passionate about driving clinical trials to success? We are looking for an experienced Clinical Trial Manager responsible for study oversight and delivery management (time, budget, quality)from start-up to closure in Germany. In this role, you'll collaborate with sponsors, investigators and cross-functional teams to bring life-changing treatments to patients. This role is for upcoming future opportunities that may arise at Fortrea. Key Responsibilities: Manage clinical trial activities from start-up to close-out, ensuring adherence to timelines, budgets and quality standards. Serve as the primary liaison between sponsors, sites, and internal teams, ensuring seamless communication and issue resolution. Prepare and participate in Investigator Meetings and prepare material for Site Initiation Visits. Validate study related materials (i.e. protocol, ICF, patient material) and prepare country specific documents Review Site Monitoring visit reports and ensures timelines are met. Manage site relationships (includes CRO related issues) Required Qualifications: Bachelor's or Master's degree required, preferably within Life Sciences or equivalent Thorough understanding of GCP, ICH Guidelines and Country regulatory environment Strong understanding of the clinical landscape and of clinical research processes, regulations and methodology Experience in leading or participating as an active member of cross functional teams, task forces, or local and global initiatives Ability of critical thinking and risk analysis Fluency in German and in English What We Offer: Work with an industry-leading sponsor and expand your leadership capabilities. Hybrid/remote options and a strong focus on work-life balance. Ongoing training, leadership programs and supportive work environment Join us in advancing groundbreaking clinical research. Apply today and be part of a team that makes a difference LI-GQ1 LI-Remote LI-Hybrid Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com. Fortrea is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. For more information about how we collect and store your personal data, please see our Privacy Statement. If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequestfortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.