Global Regulatory Associate Director CoDx’s & DigiMeds - Oncology Precision Meds NJ/NYC/PA

Employer
Advanced S&S (USA)
Location
NJ, NYC, PA, USA
Salary
On Application
Closing date
14 Oct 2020

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Discipline
Regulatory Affairs, Project Management, Regulatory Project Management
Hours
Full Time
Contract Type
Permanent
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Global Regulatory Associate Director CoDx’s & DigiMeds - Oncology Precision Meds NJ/NYC/PA

About my Client

This is a role with a company part of the Top 10 global biopharma companies with >100 years history which is one of the big 3 in Oncology and with a focus on Precision Meds used in combination with Immuno-Oncology and their other therapeutic areas, and a track record of bringing new medicines to market while having one of the most innovative pipelines in the industry.

The team is managed by a considerate, capable and mindful Vice President, who is building up the team on two sides, with Oncology and Precision Meds for clinically useful biomarkers, and with their Digital Medicines for med ed, adherence, and other patient-centric innovations, this regulatory role is one of the key bridges between the Clinical Development, Therapy Regulatory and Precision Meds teams.

Note: My client offers Digital Hiring and On-Boarding using Video Conferencing and the successful candidate will be inducted and trained remotely. During the next period, new hires will be allowed to work from home full-time, until such a time occurs when normal office working returns!
 

About this Opportunity

Are you excited by a strategic role that allows you to drive and shape scientific innovation? In this role, graded as Associate Director you will act as the CoDx RA strategist and a team member sitting alongside Global and US Regulatory Therapy Leads to support Oncology, Neuro, Immunology, Genetic and Cardio medicines development by developing the RA plans for the CODXs and / or accompanying Digital Medicines solutions with oversight for any necessary Regulatory submissions.

The role is global and this is a great opportunity for an experienced CODx or Digital Medicines regulatory professional. You might have gained your regulatory experiences with an IVD company supporting Oncology development as a vendor or in-house with a Biotech or Biopharma, in order to steer and bridge the two-parallel development workstreams. Alternatively, you might be working on Digital Medicines and want to broaden your experiences. Lastly, you might be working with a Regulator and now want to come over to industry.

You will have already provided tactical and operational support as well as coordination of associated IVD or Digital submissions to the US FDA or other health authorities. You will be a capable communicator, able to work well in matrix teams, with your own accountabilities and deliverables.

You will want a career environment where stead progress is encouraged and understand the idea that development comes with merit and aptitude. 

My Client Offers in Return  

A high-end basic salary as well as a high-performing stock plan, bonus scheme and medical insurance with shorter vesting. A full relocation is available post-Covid, whether you own a house or rent one, and you can be hired and on-boarded at home in the meantime. My client will buyout a certain amount of stock or performance bonus!
 

To Apply!

To apply for this role, please contact Matt Greig on 908-332-9157, or alternatively, please send a full CV to me at Matt@AdvTalent.com with a current cell number and preferred time to speak. ADV Talent operates a Global Data Protection policy and will not forward your details without your written consent.

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 knows 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

+44 20 7801 3380

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

Advanced Regulatory is a new recruitment organisation. Our consultants are industry known and highly experienced in Regulatory Affairs recruitment. We have assembled a team with competencies in databased contingency recruitment, Search & Selection as well as Creative & Campaign management. Our specialism is Regulatory Affairs. We know that successful submissions are underpinned not by one but many people, all working in cohesion. Whether you require a new career position or a new recruit at junior, mid or senior level, we would like to assist you. Our remit is to provide Regulatory Affairs professionals at all levels to pharmaceutical, regulatory consulting, biopharmaceutical and clinical research organisations.

Contact Us
  • Suite 8, Penhurst House
  • 352-356 Battersea Park Road
  • SW11 3BY
  • GB
  • +1 855-505-1382
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