RA Principal Associate

The RA Principal Associate will support regulatory activities within the life science sector, focusing on compliance and documentation. This temporary position is fully remote and is critical for ensuring adherence to regulatory standards.

Client Details

An organisation operating in the life science industry

Description

• Lead and execute regulatory strategies for assigned products and projects.
• Prepare, compile, and submit high-quality regulatory applications, including variations, renewals, and responses to health authority questions.
• Ensure regulatory dossiers remain compliant and up to date
• Provide regional regulatory expertise to support global development, CMC, compliance, and labeling activities.
• Liaise with regulatory authorities and support regulatory agency interactions.

Profile

A Successful RA Principal Associate Should Have

• Educational background relevant to regulatory affairs in the life science sector.
• Proficiency in written and spoken English; knowledge of additional languages is advantageous.
• Strong understanding of regulatory guidelines and compliance requirements.
• Experience in preparing and submitting regulatory documentation.
• Excellent organisational and communication skills.
• Ability to collaborate effectively with cross-functional teams.
• Attention to detail and a proactive approach to problem-solving.

Job Offer

Our Client Offers You

• A temporary position in the life science sector, fully remote

If this RA Principal Associate role aligns with your skills and interests, we encourage you to apply.