Draft, review and negotiate a variety of commercial contracts including but not limited to: vendor agreements, licensing agreements, confidentiality agreements, master service agreements, clinical trial agreements, clinical supply agreements, technical services agreements, software license agreements, safety data exchange agreements, laboratory services agreements, consulting agreements, R&D agreements, manufacturing agreements and indemnity agreements.
Provide advice and counsel on a range of legal matters pertaining to Research & Development, clinical trials, and related activities.
Negotiate with sophisticated counterparties.
Provide practical legal advice and support on business matters in a fast-paced environment.
Work with and advising business clients directly, as well as providing guidance and practical solutions.
Experience at a pharmaceutical, biotechnology, medical device, or other life sciences company.
Experience working with hospital systems and healthcare providers, and the nuances that exist as it pertains to clinical trials, is preferred.
Experience drafting and negotiating R&D Contracts including master service agreements, consulting and services agreements, licensing, research, collaborations, strategic alliances for development is preferred.
Broad-based knowledge of laws and regulations governing pharmaceutical activities with a focus on research & development and regulatory areas.