Assoc Project Manager , Start-up Sponsor-dedicated

Are you passionate about clinical research and regulatory excellence? Fortrea is seeking a Start Up Country Lead to join our team in France. This role offers a unique opportunity to lead regulatory operations for clinical trials, ensuring compliance, quality, and timely delivery of study milestones in a dynamic and global environment.

This is a sponsor\-dedicated opportunity.

Location : client's office 2 days a week (hybrid model, remote possibility)

Key Responsibilities

• Lead country\-level regulatory submissions and approvals for assigned clinical trial protocols.


• Translate and manage local language materials, including informed consent forms.


• Liaise with IRB/IEC and Regulatory Authorities to ensure compliance with ICH/GCP and local regulations.


• Manage country deliverables, timelines, and results to meet study commitments.


• Collaborate with cross\-functional teams (CRM, CRA, CTC, Finance, Legal) to ensure regulatory milestones are met.


• Oversee local vendors and site staff, ensuring regulatory processes are properly managed.


• Act as a subject matter expert in regulatory processes and contribute to SOP development and continuous improvement initiatives.

• Minimum 5 years of experience in clinical research, with at least 2\.5 years in regulatory submissions within the EU\-CTR environment.


• A scientific background (Pharmacist, PhD, or equivalent).


• Strong knowledge of regulatory frameworks, clinical trial agreements, and compliance standards.


• Fluency in French and professional proficiency in English .


• Excellent organizational, communication, and stakeholder engagement skills.


• Experience mentoring junior staff and contributing to team knowledge building.

• A collaborative and inclusive work culture.


• Opportunities for professional development and career progression.


• Competitive compensation and benefits.


• Flexible working arrangements (remote or office\-based).


• The chance to contribute to life\-changing research

If you’re ready to make a meaningful impact in clinical research and regulatory operations, we’d love to hear from you. Apply today and join a team that values innovation, integrity, and excellence.

Learn more about our EEO \& Accommodations request here .

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