O pozici
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.
Co budeš dělat
- 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.
Koho hledáme
- 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 English (additional languages are a plus).
- Solid proficiency in MS Office (Word, Excel, PowerPoint).
- Bachelor’s degree in law, economics, business, social sciences , or a related field.
- No prior industry experience required — this is an entry‑level opportunity with room to grow.
- Fluent in English and Spanish. Portuguese as well is ideal.
Benefity
- 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.
