Head of Legal

January 18

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Logo of Life Molecular Imaging

Life Molecular Imaging

Life Molecular Imaging is a company that specializes in developing innovative molecular imaging tracers. These tracers are designed to improve the early detection and characterization of chronic and life-threatening diseases, with a focus on neurodegenerative and cardiovascular diagnostics. Their lead product, Neuraceq, is a radioactive diagnostic agent used for PET imaging of the brain, particularly in evaluating patients for Alzheimer's disease and other cognitive disorders. Life Molecular Imaging aims to provide unique insights into the human body, enabling better diagnosis and personalized patient care.

Molecular Imaging • Radiopharmaceuticals • PET/CT • NeuraCeq • Alzheimer's Disease

📋 Description

• Responsible for performing, managing and supervising legal and compliance work and activities pertaining to the Life Molecular Imaging’s the US business. • Provides legal advice to corporate, commercial (sales, marketing, manufacturing, distribution, licensing, operations), medical affairs and compliance departments of the Life Molecular Imaging business either directly or via external counsel management. • Identify and mitigate legal and compliance risks, and develop and advise on the legal and compliance aspects of company policies and procedures. • Understands the needs and priorities of the LMI strategy and the business. • Drafting, negotiating, and reviewing of commercial contracts covering the entire product lifecycle and supply chain. • Support of Medical Affairs Division, in collaboration with US and EU Legal teams as needed. • Identifies risks and ensures that these are allocated appropriately to protect the business. • Develop templates and precedents to bring consistency to contractual arrangements. • Ensures legal compliance by creating, updating, implementing, monitoring, and enforcing policies, procedures, guidelines, and manuals. • Will be responsible for supporting internal and external audits, oversight of the compliance function.

🎯 Requirements

• US qualified lawyer licensed to practice in lawyer’s US state of residence. • Ten years of progressive post qualification experience in the pharmaceutical, life sciences, biotech and/or medical device industries required, with familiarity of the (radio)pharmaceutical industry in both pre-commercial (research) and post approval (FDA NDA/INDs) settings. • Experience supporting healthcare economics and market access preferred. • Demonstrable commercial awareness and acumen. • Excellent drafting and negotiation skills and experience with complex commercial agreements. • Exposure to pharmaceutical IP and licensing issues with respect to contracting and able to negotiate such issues to a favorable position for LMI. • Previous experience in dealing with applicable healthcare and nuclear regulatory and safety/environmental agencies preferred. • Knowledge and experience advising on issues regarding compliance, risk management, and data privacy and data protection required. • Budget preparation and fiscal management experience. • Five years of supervisory or management experience including employee development and performance management skills.

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