💼 Full-Time Position

Regulatory & Site Activation Specialist – Poland

🏢
IQVIA
📍 Lodz, Poland, Poland
📍
Location
Lodz, Poland
📅
Posted
June 10, 2026
Type
Full-Time
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Full-Time Opportunity: This is a permanent, full-time position with a competitive package and real career growth potential.

Job Description

**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...