**Regulatory & Site Activation Specialist – Poland (Home-Based)**

**Location:** Poland (home-based)
**Contract type:** Freelance/B2B contract
**FTE:** 1.0
**Start:** Immediately
**Duration:** approx. 3 months

**About the Role**

We are looking for a **Regulatory & Site Activation Specialist based in Poland** to support local clinical trial start-up activities with a strong focus on **regulatory submissions and site activation** . This role will act as a country-level regulatory start-up expert, ensuring compliant and timely submissions, effective site communication, and readiness for site activation under EU CTR and Polish regulatory requirements.

**Key Responsibilities**

+ Act as the primary point of contact for investigative sites in Poland, ensuring clear and proactive communication
+ Lead and manage country-level regulatory and start-up activities, including site activation processes
+ Prepare, review, and submit...