iterativehealth
Site Start-Up & Feasibility Specialist
At a Glance
- Location
- Romania or Poland
- Experience
- 3+ years
- Posted
- 2026-07-07T14:06:59-04:00
Key Requirements
Required Skills
Domain Knowledge
- Biotech
- Clinical
- Healthcare
- Pharmaceutical
- Regulatory
Requirements
Minimum of 3 years of experience in clinical research, preferably in a CRO, site start-up, feasibility, site management, or clinical research coordination role.
Experience supporting pharma-sponsored clinical trials, preferably Phase 2–4 studies.
IBD clinical trial experience is required.
Basic understanding of ICH-GCP, site operations, regulatory documentation, SSV/SIV preparation, and study activation requirements.
Experience working with clinical trial sites in Romania and/or Moldova is preferred.
Willingness to travel within Romania and Moldova for site visits as needed.
Compensation & Benefits
PLN 188,000 – PLN 225,500 gross annual base salary or RON 216,000 - RON 259,000
Fluency in Romanian and English are required, both written and spoken.
Where You'll Drive Impact
Site Identification, Feasibility & Selection
Support the collection and maintenance of information on qualified IBD clinical trial sites in Romania and Moldova.
About the Company
Collaborative and low-ego team environment
High ownership and accountability culture
Fast-paced and highly iterative growth environment
Open communication and continuous learning mindset
Mission-driven organization focused on improving patient outcomes
Comfortable navigating evolving business priorities and opportunities