• Drafts and negotiates material transfer agreements, data use agreements and confidentiality agreements with academic institutions and for-profit companies to facilitate the advancement of research projects and programs.
• Drafts and negotiates materials license agreements and elements of industry research contracts with commercial partners to support R&D and product development.
• Reviews incoming contracts and manages docketing/record system for agreements.
• Works collaboratively with licensing officers to determine the impact of the aforementioned agreements on intellectual property and to negotiate practical resolutions that balance scientist and industry needs with the mission of CTTC.
• Aids in the contractual structuring of biobanks, to support large scale biomedical research investigation.
• Oversees the transfer of research tools in compliance with patient privacy laws, rules, statutes and guidelines.
• Coordinates reviews of incoming and outgoing research tool transfers with Export Control, legal affairs, and patient de-identification authorities.
• Oversees contract compliance for CTTC technology transfer agreements, and aids in collection of payments in arrears and in resolving 3^rd party contract breaches, including renegotiation and termination duties.
• Creatively solves problems by analyzing and interpreting law and policies as well as information from other sources.
• Collaborates with and disseminates information to research staff to ensure that contractual terms accurately reflect the likelihood of intellectual property and publication and evaluates the effect of possible restrictions created by contract terms.
• Implements quality assurance and contracting strategies to achieve goals and assure compliance with all applicable requirements. Recommends changes to policies, procedures, or resources to support new strategy.
• Performs oversight and verification of, and maintains the integrity of, database entries.
• The responsibilities listed are a general overview of the position and additional duties may be assigned.

Qualifications

• A Bachelor’s degree from an accredited institution of higher education is required.
• A Bachelor’s or Master’s degree in science or engineering from an accredited institution of higher education is preferred.
• A Juris Doctor degree from an accredited law school is strongly preferred.
• Excellent writing and verbal communication, project management, conceptual, and analytical skills are necessary.
• Proficiency with negotiating material transfer agreements, confidentiality agreements, and data use agreements is required.
• Experience with drafting and negotiating industry sponsored research agreements is required.
• Experience negotiating industry materials license agreements and similar transactional documents is required.
• Experience with drafting and interpreting technology license agreements is preferred.
• Knowledge of healthcare regulations and patient privacy statutes, including HIPAA (Health Insurance Portability and Accountability Act) and the Common Rule in the U.S., and GDPR (General Data Protection Regulation) in Europe, is required.
• Experience in interpreting statute sand regulations is preferred.
• Knowledge of technology transfer and the Bayh-Dole Act is preferred.
• Knowledge of contract compliance processes is preferred.
• An ability to work effectively and productively as a member of a team and with senior management is preferred
• Ability to promote a positive culture of support and compliance with internal and external regulatory requirements is preferred.
• Ability to prioritize and multi-task in a collaborative, fast-paced environment is preferred.
• Experience with campus academic & administrative platforms or other industry related software is preferred.
• Knowledge and experience with regulatory compliance guidelines in the postsecondary education industry or a related sector is preferred.
• Significant experience working with postsecondary institutions is preferred.