pfm medical, Inc. is a subsidiary of pfm medical ag (Cologne, Germany) and was established in 2001 to serve as headquarters for North, Central, and South American development, manufacturing, marketing, and distribution activities$1. .$1
Medical Device Manufacturing
11 - 50
March 29
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pfm medical, Inc. is a subsidiary of pfm medical ag (Cologne, Germany) and was established in 2001 to serve as headquarters for North, Central, and South American development, manufacturing, marketing, and distribution activities$1. .$1
Medical Device Manufacturing
11 - 50
• Provide regulatory strategy and development guidance for clinical trials • Coordinate and prepare regulatory documents for submission • Maintain current knowledge of regulations and guidance documents • Support and enhance corporate Regulatory function • Provide ICH GCP guidance, advice, and training • Participate in maintaining and executing corporate quality initiatives
• Bachelor's degree, ideally in a scientific or healthcare discipline • 5 years Regulatory experience required for the Manager level • 7 years Regulatory experience required for Senior Manager Regulatory level • Computer literacy (MS Office/ Office 365) • Fluent in English • Previous experience working for a Clinical Research Organisation • Experience leading Clinical Submissions • Informed knowledge of drug development process and regulatory activities • Availability for domestic and international travel
• Competitive salary • Opportunities for career advancement • International travel • Ability to work remotely
Apply NowMarch 29
1001 - 5000