Expiry Date: 02-03-2020
Categories Clinical Research, Regulatory Affairs
Salary: On Application
Job Type: Full Time
R E G U L A T O R Y ** Do you want to use your US RA experience to develop towards being a GRL? **New position working in early stage development, incl. mAbs
You see yourself as an aspiring regulatory professional with a keen interest in consolidating what you have learnt, and applying yourself further to develop and stretch your skills.
Alternatively, you could be 'there already' and want to move because your current organization has plateaued so you know want a fresh challenge, a new project or product and because we have options on grading with 2 levels of grade, so it is very likely we can meet your expectations as we can hire at Senior Manager or Associate Director levels. Relevant points to consider about this organization are:-
As well as a variety of people to learn from, and although the company has a track record of developing regulatory professionals, with many of the GRLs being home-grown, this is also augmented by ex-FDA Regulators and Regulatory Professionals from other major companies including the top 5 organizations and speciality pharmaceutical companies.
To apply for this role, you will have a mimumum of 5 years' experience in regulatory affairs, more for the more senior grading, and be willing to either work remotely with travel often to HQ, or be willing to relocate or live near RTP / Raleigh Durham, NC.
A full relocation package is available to you, depending upon your location and situation.
To apply for this role, please press the red “Apply for position” button, or contact Matt Greig, on 908-332-9157 in full confidence to receive more details on this role or to hear about other available opportunities in Regulatory Affairs. Please feel free to call me during working hours or on Saturday or Sunday AM (Eastern time)!
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