Opportunity Description
Join Freyr as a Remote Regulatory Affairs Manager, facilitating Clinical Trial Authorization submissions. Utilize your skills to enhance compliance and support global Life Sciences initiatives.
As a Regulatory Affairs Manager with Freyr, you'll play a key role in supporting the Clinical Trial Submissions team. This position focuses on operational support and ensuring timely completion of submission documents in line with EU/UK regulations. Your strong organizational skills will drive quality outcomes while you collaborate with a diverse range of stakeholders.
Key Responsibilities:
• Assist in the quality control of CTA submission documents
• Track document provision and proactively engage with stakeholders
• Maintain organized trackers for submission timelines
• Document meetings and ensure actionable follow-ups
• Coordinate with various teams on submission needs
Requirements:
• Bachelor’s degree in Life Sciences or relevant experience
• 3–5 years in the b...
As a Regulatory Affairs Manager with Freyr, you'll play a key role in supporting the Clinical Trial Submissions team. This position focuses on operational support and ensuring timely completion of submission documents in line with EU/UK regulations. Your strong organizational skills will drive quality outcomes while you collaborate with a diverse range of stakeholders.
Key Responsibilities:
• Assist in the quality control of CTA submission documents
• Track document provision and proactively engage with stakeholders
• Maintain organized trackers for submission timelines
• Document meetings and ensure actionable follow-ups
• Coordinate with various teams on submission needs
Requirements:
• Bachelor’s degree in Life Sciences or relevant experience
• 3–5 years in the b...
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