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
Apply NowSimilar Jobs
September 15
Medtronic
10,000+
Lead regulatory strategies for innovative diabetes devices at Medtronic.
September 15
Penn Mutual
1001 - 5000
Compliance Director overseeing PMAM and PSF Compliance Program for regulatory adherence.
September 15
Modivcare
10,000+
Manage IT compliance and audit processes for a service-oriented health company.
🇺🇸 United States – Remote
💵 $92.5k - $124.9k / year
🔥 Funding within the last year
💰 $525M Post-IPO Debt on 2024-07
⏰ Full Time
🔴 Lead
🟠 Senior
🚔 Compliance
September 12
Catalyst Clinical Research
201 - 500
Vice President of Regulatory Affairs and Quality at Catalyst overseeing compliance and quality functions.
September 10
MCRA
51 - 200
MCRA seeks Director, Cardiovascular Regulatory Affairs for cardiac device regulatory strategy.