Senior Regulatory TA Lead ** Commutable from NJ, NYC, PA ** Exec Director or Senior Director (Code USA 220520-1)

Reference: MG220520

Expiry Date: 22-12-2020

Categories Biotech, Regulatory Affairs

Salary: Competitive

Job Type: Full Time

Location:
Mercer County
United States

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Job Description

Senior Regulatory TA Lead ** Commutable from NJ, NYC, PA ** Exec Director or Senior Director

Please consider this role if you are seeking to move from a regional team management role to a global one, for a small team of between 4-8 FTEs in a top 10 R&D-based global biotech company, reporting to a senior figure who has a well earned and brilliant reputation, both on the people and projects levels, and is a fair and highly competent manager and leader:-

  • You want to work in a company which has had a string of successes recently in the therapy area and id led by a Vice President who is equally at ease with their staff when dealing with challenging regulatory hurdles or supporting innovative thinking or smart risk-taking
  • The role can be based in either 1 of 2 sites which combined can be accessible from New York City, New Jersey and the New Jersey / Pennsylvania border areas
  • The company will buyout stock for compelling individuals and we have both the Executive and Senior Director grading – the package is commensurate as you can imagine
  • The role comes with a truly impressive relocation package if needed, and we have Covid precautions and digital hiring in place
  • This is for someone who likes to be the ‘Coach’ not always the ‘Power hitter’.

This role is not for everybody! You will enjoy working at the project level but your preferred style is that of a mentor and facilitator, a bridge builder, who works from behind the regulatory strategists as a mentor and coach, connecting with clinical and commercial to triangulate on the development strategies and build the conversational space for regulatory strategists, clinical science and the commercialization teams, with the Regulatory Strategists reporting to you - you will know how to set the right tone to enable your teams to engage globally to drive the programs forward.

So this is a leadership role, but not in the sense that you do everything yourself, the team is a mix of global and US regulatory strategists, who deliver the global RA strategy plans, as well as lead the regions globally for a varied mix of novel, small and large molecules, for a broad therapy area which includes pretty much all types of immunology and inflammation, so derma, rheuma, neuro, as well as more specialized disease areas.

To apply and to be part of this ground-breaking team, you will be an experienced manager of people, but this could be a matrix leadership style, and could be as a Senior GRL or GRL, and now you would like to grow into a direct management role. Your management style will be compatible with my description above, and you have a strong understanding from ‘doing the job’ of US and core markets drug development, leading submissions through to approvals, and how to navigate the twists and turns in development, including co-leading health authority meetings.

In return my client is offering a strong basic and bonus package, decent stock awards per annum, a willingness to buyout stock for the right candidate and if needed, a relocation package.

To Apply!

To apply for this role, please press the red “Apply for position”, or contact either myself, Theo Moore, on 855.505.1382 or my colleague (for weekends AMs and evenings), Matt Greig, on 908-332-9157. ADV Talent operates a Global Data Protection policy and will not forward your details without your written consent.

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