Offer summary

Qualifications:

Previous independent monitoring experience in clinical research., Knowledge of diverse therapeutic areas including Neuroscience, Oncology, and Infectious Disease., Ability to work remotely and manage national monitoring across Poland., Strong organizational and communication skills..

Key responsibilities:

Conduct national monitoring of clinical trials across various therapeutic areas.

Implement risk-based monitoring strategies for effective trial management.

Collaborate with cross-functional teams and stakeholders in the clinical research process.

Participate in on-site visits and ensure compliance with protocols.

Job description

Our multi-sponsor Team in Poland is looking for a passionate CRAII 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.

Please note: The ideal candidate should be based in Warsaw or in the south of Poland (e.g. Kraków, Katowice).

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.

Required profile