Join Fortrea as Site Navigator and serve as a local expert in project Start - Up Activities for Portugal!
Responsibilities:
- Preferable Site Identification experience / Feasibility.
- Contract and budget negotiation with sites minimum 1 year (preferable sites in Portugal)
- Coordinate, collect essential documents and organize data and information required by EC/Third body/Regulatory Authority according to regulatory legislation, guidance, and practice in the assigned countries.
- Preferable PSV remote experience.
- Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.
Experience Required:
Minimum of 2 years of experience in clinical development or start-up/ regulatory process.
- Working knowledge of ICH, RA, IRB/IEC, and other applicable regulations/guidelines.
familiarity with investigator start-up documents and contract/budgets negotiation process.
previous interaction with operational project teams and investigative sites.
- Demonstrated understanding of research protocol requirements and proven ability to communicate them/educate others about them.
Qualifications (Minimum Required):
- University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology) AND 2 years' work experience in clinical research, including a strong working knowledge of the ICH guidelines and RA, IRB/IEC regulations.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Benefits:
At Fortrea, we value our team members and offer a comprehensive benefits package, including competitive compensation, health and wellness programs, and opportunities for professional growth. You’ll also enjoy flexible work arrangements and the chance to make a meaningful impact in cutting-edge clinical research.
Learn more about our EEO & Accommodations request here.
