Dr. Oliver’s experience spans 12 years in academia and 24 years in both the public and private sectors of the biotechnology/pharmaceutical industry and contract research organizations.
He served in numerous clinical development operations roles including Chief Operating Officer, SVP Clinical Research and Regulatory Affairs, Chief Science Officer, and Medical Officer. Throughout his career, he successfully managed large cross-functional project teams with internal staff and oversaw CRO vendors. Dr. Oliver has significant FDA experience with both the Drug and Biologic divisions, having prepared more than 50 INDs and participated in seven successful NDA submissions for U.S./Global pharmaceutical companies. In his tenure with public and private biotechnology companies, he participated in several series of successful fundraisings. In addition, Dr. Oliver has served in licensing negotiations and out-licensing of several oncology assets.
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