To provide legal support to the Clinical Development Center (CDC) and also support pharmaceutical clinical development activities, commercial contracting, legal risk assessment, data privacy, regulatory compliance and research-related agreements.
Draft, review and negotiate clinical research and pharmaceutical-related agreements, including Clinical Trial Agreements (CTAs), Confidential Disclosure Agreements (CDAs), Data Sharing Agreements, vendor contracts and other research-related documentation.
Provide legal advice on key contractual provisions covering indemnification, liability, insurance, intellectual property, confidentiality, publication rights, data privacy and other commercial risks.
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