WHY CHOOSE MEDSIR

We are a Barcelona-based fastest-growing company founded by scientific experts . We are dedicated to the design and management of innovative strategic clinical trials in oncology, from study conception to the publication of study results . Together, we create the best strategies that are both clinically relevant and scientifically meaningful . We strive to improve our knowledge of this complex disease and the vast array of available treatments in a fast-innovative way .

At MEDSIR, you will have the job of your life while working together towards our shared mission bringing novel treatments to cancer patients worldwide. We welcome top performers that will bring new ideas, diverse perspectives, and provide you the opportunities and freedom to grow and make a real impact in patients' lives and science… all while having great fun .

ABOUT THE OPPORTUNITY

As a Clinical Research Associate (CRA) II/III, you will play a key role in ensuring the successful execution of oncology clinical trials. You will combine on-site monitoring activities (if needed)



with leadership responsibilities, acting as a liaison between sites, CRAs and cross-functional teams.

HOW YOU WILL CONTRIBUTE:

· Site Monitoring Support & Training: Conduct pre-study, initiation, routine monitoring, and close-out visits to ensure protocol compliance, ICH-GCP, and regulatory requirements. Provide guidance and training to site staff on recruitment strategies, protocol updates, and data entry practices.

· Patient Safety & Data Integrity: Oversee patient recruitment and enrolment processes, review source documentation, CRFs/eCRFs, and resolve data discrepancies in collaboration with site staff and cross-functional teams.

· Investigational Medicinal Product (IMP) Oversight: Manage IMP logistics end-to-end, including forecasting, shipment coordination, and accountability. Ensure proper handling, storage, and chain-of-custody compliance, and address discrepancies identified by CRAs or site pe

📌 CRA II/III (España)
🏢 MEDSIR
📍 España