Director Regulatory Affairs - Clinical CRO

Posted 24 May 2023
Salary Competitive
LocationEurope
Job type Full Time
Discipline Clinical & Data
Contact NameJack Dean

Job description

Mantell Associatesis partnered with a rapidly growing Oncology CRO, who is looking to expand their European team.

Responsibilities - Director Regulatory Affairs:

  • Support effective Regulatory strategies by maintaining Policy and Intelligence

  • Be at the forefront of new and developing regulations and guidelines

  • Responsible for providing an overview of RA Policy to stakeholders and staff

  • Ensure submission publishing is well executed and on time

  • You will work with the Vice President of Regulatory Affairs and all Regulatory staff across the organisation

  • Engage and support all relevant staff to support M&A activities

  • Proactively manage an RA network externally and internally

Requirements – Director Regulatory Affairs:

  • You must have minimum of 10+ years of experience with RA in Pharmaceutical field

  • Proven track record of Global Regulatory Processes

  • An outstanding knowledge of Drug Development Process

  • 5+ years in Oncology

Mantell Associates is a specialist Pharmaceutical and Life Sciences headhunting firm. For more information get in contact with Jack Dean at +44 203 3854 7728 or jack.dean@mantellassociates.com.