Parexel
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+
💰 Venture Round on 1990-01
Vice President - Technical Clinical Regulatory Affairs SME - Oncology
September 15
Parexel
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+
💰 Venture Round on 1990-01
Description
• Senior role influencing clinical development strategies • Work on a variety of assignments from home • Lead project teams in regulatory consulting
Requirements
• MD or PhD required • Minimum 15+ years experience in Clinical Development/Clinical Trial Design • Expert level industry knowledge • Previous experience with a regulatory agency (FDA or MHRA) preferred • Extensive Oncology experience required • Ability to travel up to 20-30% domestically and/or internationally
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