Regulatory Manager or Senior RA Manager – Relocation Offered! Deliver line extensions and a PIP for a major biopharma!

Reference: MG080519

Expiry Date: 07-11-2019

Categories Clinical Research, Regulatory Affairs

Salary: On Application

Job Type: Full Time

Location:
Belgium

Apply for position

Job Description

 

Regulatory Manager or Senior Regulatory Manager, work on a high profile biologics product for New Indications and Paediatrics!

Note please: This role is offered to anyone in Spain / France / Netherlands / UK or anywhere in the EU and comes with a full relocation package to Belgium, including temporary apartment, disturbance allowance and tax reduction package. To apply, please contact Matt or Theo, and we will help you every step of the way!

My client is a European Bio-/Pharmaceutical company which is steadily expanding and is now seeking to hire a Manager or Senior Manager to work in their European therapeutic regulatory group, in Brussels, Belgium. This role will appeal to you if you find yourself answering yes to these questions:

  • Do you want to work on a high value biologic to deliver clinical line and label extensions then switch to a NBE for an MAA after?
  • Do you have experience of PIPs, CTAs, and have assisted on MAAs or major variations and now want to gain more Centralised Procedure experience?
  • Are you looking to work in a company where you can be developed, have accountability for delivering your own projects and can eventually grow to be a GRL?
  • Do you want to switch to the immunology therapy area? In a company which has 6 NBEs in development, 5 of which in Ph2/3, so there are plenty of new opportunities to grow with?

Initially you will work on a Centralized Product, which is a blockbuster, to start with on Line Extensions and a PIP, before moving to a another program later, a NBE for preparation of the first-line MAA.

In return for the above, you will have either worked on CTAs and Scientific Advices with some lifecycle management experience, or have worked on MAAs and lifecycle and want to gain full project lifecycle experience. Alternatively, you might have worked in a CRO, on CTAs, and Orphans, this would also be useful. English is the spoken business language and the company is very multi-cultural.

The company has a merit based advancement process so if you work hard, deliver with passion, and are a likeable individual, you will do well! The line managers, and GRLs, at this client of ours, all started in this role, so you have plenty of opportunity to do the same as well as people to learn from.

It is not mandatory, but it is likely you will have between 2.5 and 5 years’ experience in “regulatory” and would be happy with a Regulatory Manager or Senior Regulatory Manager level grade. The company offers a decent bonus scheme plus full health insurance and relocation.

 

To Apply!

To apply, please contact either myself Matt on + 44 20 7801 3380 or my colleague Theo on + 44 20 7801 3384, or send a full CV to cv@advtalent.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.

GDPR & Data Protection: Your information is safeguarded for GDPR, and you will have the right to edit, amend or delete and ’’be forgotten’’ at any time after your initial registration.

We provide a high level of service because we believe this matters.

Keywords / Key words: Regulatory Affairs, RA, RA Jobs, Regulatory Affairs Jobs, RA Manager, Regulatory Jobs, Regulatory, Biopharmaceutical Jobs, Biopharma Roles, Biotechnology, Biopharma, Pharmaceutical, Pharma, Bio-pharmaceutical, Bio-technology, Spain, Global Regulatory Affairs, Snr Regulatory Affairs