Senior Regulatory Manager

Key People

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Job ID :


Company Type :

Staffing Firms

Industry :


Education Level :


Address 1 :

United Kingdom,--West London,West London,

Key Skills :

regulatory affairs, clinical trial applications, CTA, EMEA, PIP, CP, centralised procedure

Salary :

£65 - £85 per hour

Date Posted :

01 Mar, 2019

Company Name :

Key People

Location1 :

West London

Job Category :

Regulatory Affairs Jobs

Experience :


Job Type:


Travel Amount:



Within this role you will provide regional regulatory support for multiple products. It is essential that you have STRONG strategy and recent EMA clinical experience.

You will have a strong background supporting the diversity of regulatory procedures in the EU (inc. PIPs, variations, IMPDs, MAAs) and ability to work autonomously. The purpose of this role is to progress the client pipeline through timely regulatory approvals, including clinical trials for investigational medicinal products, as well as approved medicinal products, and to ensure timely regulatory compliance with such approvals.

- Define and advise the GRT on regional considerations in developing creative regulatory strategy
- Ensures European regional needs are well defined and implemented in collaboration with relevant regional stakeholders
- Develops and implements regulatory strategy and executional plans, and manages regulatory submissions (e.g. clinical trial and marketing applications) for assigned products in accordance with global filing plans, core labelling documents and regulatory requirements
- Leads development of regional regulatory documents and meetings, and provides regulatory advice on regional regulatory requirements, mechanisms to optimize product development and to maintain compliance
- Co-ordinates and provides guidance to company responses to requests from regulatory authorities, e.g Response to Questions (RTQs)
- Communicates and ensures alignment with proposed regulatory strategies such that expectations, regulatory risks and mitigations are characterised and understood.
- Estimate the likelihood of regulatory success and timelines based on proposed strategies; discuss with GRT and line Management, and communicates to stakeholders
- Maintains an awareness of new and developing legislation, regulatory policy and technical Regulatory guidance relating to company products, and evaluates and communicates impact
- Act as contact and create relationships with agency staff on specific product assignment and document and communicate details and outcomes of regulatory agency interactions

Basic Requirements:
- Demonstrable experience acting as therapeutic area European Regulatory Affairs lead, defining and implement regulatory strategies and executional plans
- Practical Regulatory knowledge of regional legislation
- Working with policies, procedures and SOPs
- Experience with national legislation and regulations relating to medicinal products
- Understanding of the regional regulatory procedures for CTAs, MAs, post approval changes, extensions and renewals
- Understanding of drug development
- Centralised Procedure
- Strong knowledge of and experience in regional regulatory environment in relevant product area and development stage
- Comprehensive understanding of regulatory activities, touch points and how they affect projects and processes
- Ability to resolve conflicts and develop a course of action leading to a beneficial outcome
- Cultural awareness and sensitivity to achieve results across both regional country and International borders

Preferred Requirements:

- Experience in oncology therapeutic area
- Experience working with biotechnology products

Please call Tim Barratt on 01727 817626 or email

Company Name:

Key People


Catherine House,Adelaide Street


Staffing Firms


United Kingdom





less than 100




St Albans

Phone No. :

01727 817 626

Key People is a recognised leading supplier of staffing and recruitment services to the Pharmaceutical, Scientific & Biotech industry. The company has been operating for over 20 years and has an integrated team of qualified recruitment consultants averaging more than 7 years of recruitment experience. Each consultant is a specialist recruiter for their market area, so they can provide full market advice to candidates and clients alike.

For more information,visit

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