Perspective Therapeutics
51 - 200 employees
Founded 2023
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $400k Grant on 2024-02
Biotechnology • Healthcare Insurance • Pharmaceuticals
Perspective Therapeutics is a biotechnology company focused on developing innovative cancer treatments through a unique class of theranostics. Their proprietary technologies enable the targeting of specific tumors for treatment while minimizing toxicity to healthy tissues. By utilizing radiation, radiopharmaceuticals, and advanced imaging technologies, they aim to improve treatment efficacy and provide better outcomes for cancer patients.
Executive Director, Global Regulatory Lead
🕒 April 30
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Perspective Therapeutics
51 - 200 employees
Founded 2023
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $400k Grant on 2024-02
Biotechnology • Healthcare Insurance • Pharmaceuticals
Perspective Therapeutics is a biotechnology company focused on developing innovative cancer treatments through a unique class of theranostics. Their proprietary technologies enable the targeting of specific tumors for treatment while minimizing toxicity to healthy tissues. By utilizing radiation, radiopharmaceuticals, and advanced imaging technologies, they aim to improve treatment efficacy and provide better outcomes for cancer patients.
📋 Description
• Provide strategic regulatory leadership across radiopharmaceutical clinical development programs • Develop and execute global regulatory strategies • Lead global regulatory submissions in support of clinical development, product registrations, and lifecycle management activities • Translate complex and evolving global regulatory requirements into clear, actionable strategies • Ensure regulatory alignment across functions and support the successful advancement of radiopharmaceutical programs from early development through commercialization
🎯 Requirements
• Bachelor’s degree in a scientific or life sciences discipline required; advanced degree (M.S. or Ph.D.) in biology, chemistry, pharmaceutical sciences, engineering, or a related field strongly preferred • Regulatory Affairs Certification (RAC) is a plus • Minimum of 10 years of progressive Regulatory Affairs experience within oncology, specialty therapeutics, and/or complex modalities, with demonstrated regulatory leadership and successful global development outcomes • Experience supporting radiopharmaceutical, oncology, or other complex drug modalities, with a strong understanding of modality‑specific regulatory considerations • Proven track record of leading major global regulatory submissions and approvals, including INDs, CTAs, and marketing applications, for clinical‑stage and/or commercial products • Extensive experience engaging with global health authorities (e.g., FDA, EMA, and other international agencies)
🏖️ Benefits
• Remote, home-based position • Ability to sit for extended periods of time while working at a computer and participating in virtual meetings • Ability to use standard office equipment, including a computer, phone, and video conferencing tools
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