Associate - Oncology Material Licensing
Location
United States
Posted
35 days ago
Salary
$58.5K - $150.7K / year
Seniority
Mid Level
No structured requirement data.
Job Description
Associate - Oncology Material Licensing
Eli Lilly and Company
Role Description Do you have expertise negotiating and managing material licenses and transfer agreements in a life sciences research setting? If so, consider joining the Lilly Oncology Business Unit (OBU). This is an exciting time to be part of the OBU, as we boast an expansive pipeline, robust scientific expertise, and a proven team dedicated to making a difference. In this role, you will support the material licensing and transfer needs of our early phase oncology research teams, enabling scientists to access the tools, models, and biological materials that are critical to discovering the next generation of cancer treatments. Be a part of our mission to improve patient outcomes and make a lasting impact in the field of oncology. The Associate, Oncology Material Licensing in the Business Operations team is a skilled individual contributor within the Early Phase Oncology organization, responsible for executing the full lifecycle of material licensing and transfer agreements that enable scientific research. - Assess incoming material requests. - Negotiate material transfer agreements and license agreements for cells, plasmids, animal models, and other proprietary biological materials. - Maintain accurate records of licensed materials and associated use restrictions. - Operate with a strong sense of ownership within their portfolio. - Escalate complex issues to team leadership with well-formed options. - Contribute to the team’s overall effectiveness by executing reliably and communicating proactively. Qualifications - Bachelor’s degree required; degree in biology, biochemistry, or a related life sciences discipline preferred. - 3+ years of contract management experience, including negotiating and managing material transfer agreements and license agreements, preferably in a biotechnology or pharmaceutical setting. - Qualified applicants must be authorized to work in the United States on a full-time basis. Requirements - Scientific literacy and the ability to engage credibly with research scientists regarding biological materials. - Demonstrated ability to manage an assigned portfolio of agreements accurately and on time. - Ability to make consistent, sound decisions within established contracting frameworks. - Strong contract drafting, review, and analysis skills. - Working knowledge of key legal and commercial provisions common to material licensing and transfer agreements. - Ability to apply scientific knowledge to evaluate material transfer requests. - Strong organizational skills with the ability to manage a high volume of concurrent material requests. - Commitment to becoming proficient in Lilly’s contract lifecycle management (CLM) system. - Strong written and verbal communication skills. - Excellent attention to detail and critical thinking skills. - MS Office skills (Outlook, Word, Excel, PowerPoint). - In-depth knowledge of early phase drug discovery and development. - Experience with project management, procurement, and contract lifecycle management software. - Experience negotiating and managing in-licenses for biological materials. - Fluency with AI tools and a willingness to apply emerging AI and automation solutions. Benefits - Eligibility to participate in a company-sponsored 401(k) and pension. - Vacation benefits. - Eligibility for medical, dental, vision, and prescription drug benefits. - Flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts). - Life insurance and death benefits. - Well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).
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