NEW - Associate Director CoDx Regulatory *Post Covid Cadillac Relo to PA/NJ or NJ/NYC*

Advanced S&S (USA)
On Application
Closing date
14 Oct 2020

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Clinical Research, Clinical Operations, Clinical Research Scientist, Regulatory Affairs
Full Time
Contract Type
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NEW - Associate Director CoDx Regulatory *Post Covid Cadillac Relo to PA/NJ or NJ/NYC*

About My Client

This is a role with a Top 5 global pharma company which occupies an exclusive niche position with a focus on novel products across with 4 major therapy areas and over 100 years' history and track record of bringing new medicines to market while having one of the most innovative pipeline in the industry currently. Their pipeline and this role includes oncology.

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 working returns!

About this Opportunity

Are you excited by a strategic role that permits you to drive and shape scientific innovation, provide tactical and strategic input into developing the regulatory pathways for CoDx in oncology and other speciality disease areas?

Do you want to work with therapy regulatory leaders to provide input, translate Precision Meds biomarker targets into IDEs and final Dx registrations?

Are you interested in widening your experience form CoDx's into digital medicines, for your assigned programs?

Can you lead / coordinate and drive complicated CoDx programs with the partners, for adaptive design Clinical Trials and quick changing oncology programs requiring Clin Trial Assays, risk assessments and IDE filings? (Although you will work across all TAs).

About you!

You will have already worked in IVDs, and CoDx's in a regulatory role, and this could be with a sponsor side role in a biotech or pharmaceutical company, or with one of the CMOs and vendors who specialize in IVDs for companion or complimentary use, and have good exposure / or direct experience of working with drug development teams. You will have a solid track record in work history terms, and be willing to relocate this year or next to either NJ/PA borders or NJ/NYC, if needed.

Package & Benefits

You will benefit from an annual stock award with a quicker vesting period, a decent salary and performance bonus in a company which regularly gives good performance multipliers for dedicated employees, as well as a high end Associate Director basic. The company will buy out stock within reason and 2020 bonuses if you lose these.

To Apply!

To apply for this role, please send your CV to, or contact Octavian Dinca on US toll free 855.505.1382 in full confidence to receive more details on this role or to hear about other available opportunities. 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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