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Precision Medicine Group
Regulatory And Start Up Specialist
Remote · UK · Full time · Mid level
About the role
Manage site activation readiness and regulatory submissions for clinical trials in the UK. Ensure compliance with local and international regulations and support contract and budget negotiations.
What you’ll do
• Deliver site activation readiness on time and quality. • Prepare clinical trial application forms and submission dossiers. • Interact with Competent Authorities and Ethics Committees. • Maintain project plans and regulatory intelligence tools. • Support contract and budget negotiations for study sites.
What you’ll bring
• Bachelor's degree in life sciences or related field. • At least 2 years relevant experience in CRO or pharma. • Experience with regulatory submissions and site start-up. • Strong communication and organizational skills. • Legal authorization to work in the UK.
Life at Precision Medicine Group
Equal opportunity employer with commitment to diversity and inclusion. Provides reasonable accommodations for disabilities.
About Precision Medicine Group
Precision Medicine Group is a global Clinical Research Organization specializing in precision medicine, rare diseases, and oncology clinical trials.