Offer summary

Qualifications:

Previous independent monitoring experience in clinical trials., Educational background in life sciences, medicine, or related fields., Strong understanding of clinical trial processes and regulations., Ability to work independently and manage multiple protocols..

Key responsibilities:

Conduct national monitoring across Poland remotely.

Manage multiple clinical trial protocols across various therapeutic areas.

Implement risk-based monitoring models for trial management.

Maintain communication with sites and ensure compliance with study protocols.

Job description

Our multi-sponsor Team in Poland is looking for a passionate CRAI with previous independent monitoring experience to work across a diverse range of therapeutic areas. This is your chance to gain hands-on experience in groundbreaking clinical trials while being part of a supportive, fast-paced and innovative global CRO.

What You Can Expect:

✅ National monitoring across Poland (remote-based)
✅ Exposure to multiple protocols across Neuroscience, Cell/Gene Therapies, Oncology, Respiratory, Cardiovascular, Infectious Disease, Nephrology, Endocrinology & Gastroenterology among others
✅ Risk-based monitoring model for smarter trial management
✅ 8+ on-site days per month

At our global CRO, we blend 30 years of expertise with innovation, offering:

🌟 Personalized development plans & career progression
🌟 A supportive environment with flexible Line Managers
🌟 Exciting collaborations with biotech & biopharma pioneers

Make a real impact in clinical research while building your career with a company that invests in your growth and success!

Ready to make a difference? Let’s connect!

Learn more about our EEO & Accommodations request here.

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