Site Contracts Associate I 2 - German Speaker

**When our values align, there's no limit to what we can achieve.**   At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Are you ready to step into a role where legal precision meets real‑world impact? As a **Site Contract Associate**, you’ll be the driving force behind the agreements that make clinical trials possible. If you thrive on negotiation, communication, and keeping complex processes running smoothly, this is your chance to shine.   **This is a homebased role but you must be living in Poland. Fluent in German language a requirement. As well as Polish and English.** **What You’ll Do** ------------------ You’ll become the go‑to expert for **site agreements**, ensuring every contract supports the success of clinical trials across your region. Your responsibilities will include: * **Drafting & negotiating contracts** — clinical study agreements, service agreements, team member agreements, and related documents. * **Interpreting site feedback** within local legal and business frameworks to guide internal decision‑makers. * **Ensuring compliance** with ICH‑GCP, local laws, and internal guidelines. * **Acting as the communication hub** between internal teams, site staff, and external partners. * **Managing the full contract lifecycle** — from first draft to final signature and archival. * **Building strong relationships** with clinical trial sites and internal stakeholders. * **Spotting risks early** and collaborating with the Site Contract Lead to resolve them. * **Tracking progress** in real time and keeping teams informed. * **Driving process improvements** to make contracting faster, clearer, and more efficient.   **What You Bring** ------------------ You’ll excel in this role if you have: * **Strong negotiation skills** and the diplomacy to navigate complex conversations. * Excellent written and verbal communication. * A talent for problem‑solving and analytical thinking. * The ability to work confidently in a virtual, global team. * Grace under pressure and a polished, professional presence. * A sharp eye for detail and a commitment to quality. * Fluency in **German,** Polish, ad English, (additional languages are a plus). * Solid proficiency in MS Office (Word, Excel, PowerPoint).   **Education & Experience** -------------------------- * Bachelor’s degree in **law, economics, business, social sciences**, or a related field. * No prior industry experience required for **level I** — this is an **entry‑level opportunity** with room to grow.   **Why This Role Matters** ------------------------- Every clinical trial depends on clear, compliant, and timely agreements. As an SCA, you’ll help ensure research teams can focus on what matters most: bringing new treatments to patients who need them.