ONCOLOGY ** Senior GRL **Global RA strategy & leading for promising, complex ONCOLOGY programme**

Location
East Coast / Tri-State
Salary
Competitive
Posted
12 Nov 2019
Closes
12 Dec 2019
Ref
* MG/JAN0001A R9
Contact
Matt Greig
Hours
Full Time
Contract Type
Permanent
Experience Level
Management

ONCOLOGY ** Senior GRL ** High impact Global role for strategy & then leading all RA regions for 1 of the most complex ONCOLOGY programmes ** East Coast * Relocation offered
     
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This is one of those positions we receive which is very compelling for the right individual, an individual with a strong track record in leading US or global submissions, who lives and thrives on the complexity of managing global regulatory programmes with multiple indications, across many Tumor types, and at the same time, you see your role as one of bringing a narrative to each programme, a message which regulators, patients and medics, will understand through your regulatory narrative.

You will know who you are. This role is not for the faint-hearted, you will be an individual who is thoroughly organized, understands the “ How to’s ” – influence and shape strategy with the R&D folks including clinical protocol designs (in a company where regulatory has a seat at the table); with the US or the major Regulators too, as a project team to showcase the innovation and potential of the MOAs, identify rationale for SPAs or adaptive designs, and, with the regional RA leads, to bind in their inputs to your overall strategy and then deliver and seamlessly execute the overall regulatory strategy you are accountable for and know how to show case.

You will be parachuted into this major programme, with very promising data, a highly supportive management team, and, even though this is a large bio-pharma, a close knit collegiate feel, to be the Global RA Strategy Lead for a programme with 10s’ of indications in Phases 2a/2b and with Phase 3s pending, and a clear remit to drive this programme through to NDA/MAA & sNDAs globally.
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You will be an individual who can see beyond the initial strategy to what the patients and prescribers require in each patient segment and for each indication, and by collaborating with the cross-functional experts, help the project team translate these into a clearly differentiated studies, through to read out and major submissions / review. My client is known for innovative sciences that enable the innovation you want to see in the MOA, primary and secondary protocols incl. biomarkers and subsequent filings.  

In return, my client is offering a world-class package underpinned by a merit-based advancement and compensation model, which combines high end salary, bonus and LTIs for the right individual. For the right candidate, my client will buy out RSU and Stock plans, and provide a red carpet relocation to the East Coast / Tri-State area.

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To apply, please contact one of our two Senior Recruiters, either myself or my colleague Matt Greig or Theo Moore on US Toll Free >  855.505.1382  < or send a full CV to cv@advregulatory.com and we will respond by return. We are assigned these roles by our client and will provide you with support throughout the hiring process.
     
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About Advanced Search & Our Network

Advanced Search, has a network of affiliated companies including ADV Regulatory, and ADV Talent Partners. Together, we are specialists in Regulatory Affairs and Life Sciences recruitment especially around mAbs and biologicals for roles in R&D and Commercialization and have been established and hiring in this area since 2005.

Our team know our subject matter areas and our mission is to help you grow your career each and every step of the way. We have helped many of today's leading companies develop strong regulatory sciences functions and are known for hiring complimentary teams that work well with each other, at owner-contributor, strategy leading and people management levels.

Contact us today to see how we can help you make that next career move on US toll free 855.505.1382

All applications are kept in confidence and we invite applications from all members of the Academic, Research & Development based bio-/pharmaceutical community.

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