Expiry Date: 20-06-2020
Categories Biotech, Clinical Research, Regulatory Affairs
Salary: On Application
Job Type: Full Time
Location: NJ, USA
Are you an experienced RA Project Manager and running out of options to develop your career where you are? Because of company changes or outlicensing of your main product? Have you filed INDs, sNDAs, prepared for Scientific Advice and now want to gain more responsibility, and file fist line NDA submissions and complex Line Extension New Indications with a better financial package and in a company where there are ample opportunities to shine?
My client and I are seeking individuals who are high-performing with engaging personalities who want to grow and learn, and be in a company where there are plenty of capable people to work with and learn from. You will already have experience in regulatory project management, and have started to identify that you could do more of a senior role, with more strategic involvement, and in time, and based on merit, develop into a Global Regulatory Leader, but in order to do this, you want to work on a high profile submission, to be able to propel you forward and create that formative set of experiences global strategy regulatory leading requires.
In return for your energy, dedication and existing regulatory project management capabilities, my client is offering a great starting point, a relocation package if needed which includes house purchase / sale, and a competitive package and bonus package and health insurances. My client allows 3 days in, 2 days out, so there is some flexibility on home / office working, and an environment where you will see, expand and learn new ideas and ways of approaching common challenges, backed up by a leadership team which is (and I mean located in the same area and offices) there to really help you get the most out of your role!
To apply for this role, please press the red “Apply for position” button, or contact Theo Moore or Matt Greig on US Toll Free 855.505.1382.
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