Parexel Is Hiring A Senior Cra

Join Parexel FSP as a Senior Clinical Research Associate (CRA) and play a vital role in overseeing clinical trials across Italy and Spain, ensuring patient safety and study quality. 🌍

Senior CRA Opportunity at Parexel FSP 🇪🇺

Parexel FSP is actively seeking an experienced Senior CRA to collaborate with one of our key sponsors in the European Union. In this pivotal role, you will supervise clinical trial sites located in Italy and Spain, maintaining high standards of trial conduct and patient safety.

Key Responsibilities 📝

• Ensure compliance with the Study Monitoring Plan, Good Clinical Practices (GCP), and applicable laws to guarantee the proper conduct of clinical trials.
• Manage operational activities at investigator sites, from site activation through database lock, ensuring timelines and quality benchmarks are met.
• Coordinate communication between study team members, vendors, and investigator sites to facilitate smooth information flow.
• Monitor safety reports such as AEs and SAEs, collaborating with the Drug Safety Unit and investigators to resolve issues promptly.
• Serve as audit point of contact by supporting audit processes, developing CAPA plans, and following up on observations when necessary.

About Parexel 🌟

Parexel supports clinical research across diverse therapeutic areas, fostering long-term partnerships with a broad client base. We have contributed to trials for many of today’s top 50 best-selling drugs and also support niche developments vital to patient well-being. Join us to be part of a global team making impactful advances in healthcare.

What We Are Looking For 🎯

We seek professionals dedicated to placing patient well-being at the forefront—a team working with heart and determination.

Role-specific requirements include:

• Bachelor’s degree in life sciences, nursing, pharmacy, medical background, or equivalent.
• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA, and local regulations.
• Monitoring experience: Minimum 3.5 years in clinical research site monitoring, preferably in Oncology.
• Therapeutic experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases is preferred.
• Qualified candidates must have monitoring experience across both Italy and Spain.
• Fluency in English, Italian, and Spanish is essential.

#LI-REMOTE

EEO Statement 🤝

Parexel is an Equal Opportunity Employer. We welcome qualified applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. We are committed to fostering an inclusive environment for all.