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Regulatory Affairs Project Manager

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Paris, Île-de-France Excelya Temps plein
Join Excelya's Team as a Clinical Studies Regulatory Affairs Specialist

We are seeking a highly skilled Clinical Studies Regulatory Affairs Specialist to join our team at Excelya. As a key member of our Clinical Studies Regulatory Affairs Team, you will play a crucial role in ensuring the success of our clinical trials by providing expert regulatory guidance and support.

Key Responsibilities:
  • Develop and implement operational regulatory strategies for clinical trials, ensuring compliance with regulatory requirements and industry standards.
  • Collaborate with cross-functional teams to design and execute clinical trials, leveraging expertise in regulatory affairs and clinical operations.
  • Provide regulatory support and guidance to project teams, ensuring that all aspects of clinical trials are conducted in accordance with regulatory requirements.
  • Stay up-to-date with regulatory developments and changes, ensuring that Excelya's clinical trials are compliant with the latest regulations and guidelines.
What We Offer:

As a Clinical Studies Regulatory Affairs Specialist at Excelya, you will have the opportunity to work on a wide range of projects, collaborating with a talented team of professionals who share your passion for regulatory affairs and clinical trials. We offer a stimulating work environment, opportunities for professional growth and development, and a competitive compensation package.

We are committed to empowering our team members to excel in their roles, providing them with the tools, resources, and support they need to succeed. If you are a motivated and experienced regulatory affairs professional looking for a new challenge, we encourage you to apply for this exciting opportunity.