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Job Details

Director, Global Clinical Development - Neurology - Germany, Belgium or UK based

Company: Advanced S&S (Medical / Clinical)
Location: Germany, Belgium or UK based
Reference: TMADV / 160816A
Closing Date: 15 Dec 16
Type: Full Time
Salary (£): 100,000+
Benefits: On Appplication

Job Summary:

This role is on exclusive assignment to Advanced Search & Selection. Please contact Theo Moore or Matt Greig initially on +44 20 7801 3380 or +44 7918 679 405 (until 9.00 pm CET and Saturday mornings) or send a full CV and contact information to theo@advregulatory.com or matt.greig@advregulatory.com who will support your assessment and onboarding process.

Requirements:

Global Clinical Project Director and Associate Director - Neurology

Location: Germany, Belgium or UK based

Our client is a global biopharmaceutical company focused on the discovery and development of innovative medicines for the nerve system, but is very different from other top 20 organisations, as they are not departmentalised or rigid in approach and have not grown through buying a number of other companies each year. This organisation has grown and developed by having a dynamic, innovative and entrepreneurial approach to drug development and product registrations and has considerably expanded its marketed products globally.

They are now recruiting for a number of Clinical Project Directors and Associate Directors for broad-based, strategic leadership roles for their highly regarded Neurology franchise. As well as ensuring that clinical trial activities are executed efficiently (e.g. within agreed timelines and budget) and to a high standard, meeting all appropriate regulatory requirements, you will represent the company and speak at conferences, symposia and meetings with Key Opinion Leaders.

These roles are a good mix of strategic input and global project management, and cover early and mid-phase development for biologicals. You will need enormous drive and enthusiasm, with the ability to inspire your team and the wider group to perform and achieve to a higher level. You will also be a savvy communicator with stakeholders and be used to ensuring buy-in to shape global strategies with the development, regulatory and commercial stakeholders.

Package:

The salary and packages for theses role are excellent and include a strong basic salary and bonus, with a very generous LTI package and options to work 2-3 days a week from home.

Responsibilities:

You will be responsible for all clinical aspects of the relevant development program(s) and accountable for clinical strategy and leading the development and execution of the clinical development program, including but not limited to:

  • Responsible for planning, designing, defending, and ensuring implementation of the Clinical Development Plans (CDP) enabling successful regulatory filings, approvals and launches of NCEs/NBEs and additional approvals of new line extensions (indications or formulations) of registered compounds.
  • Prompt identification of safety or efficacy results that warrant re-evaluation of project plan and/or potential termination prior to registration.
  • Develop and maintain excellent working relationships and global cross functional collaboration, between the PVU and Practice, to ensure broad high quality medical, scientific, regulatory, commercial and external input into the clinical programs.
  • Develop a strong knowledge base of the relevant therapeutic area and drug development issues and become a company expert for the respective treatment to ensure that study concepts, Protocol Summaries and final protocols related to the relevant development plans are high quality, state of the art and aligned with related Clinical Development Plans and Target Product Profiles and is appropriately managed by the clinical study team(s).

Your profile:

  • MD Status
  • Previous experience in pharmaceutical clinical development including the management of multiple clinical studies
  • Experience in writing and/or participation in the preparation of submission documents
  • Knowledge of all aspects of the clinical development process and of the relevant therapeutic area preferred

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If you wish to apply for this role, please send your CV with a covering note to cv@advregulatory.com or alternatively, to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
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About Advanced

Advanced Search and Selection - Clinical and Medical Division has been operating since 2004. We are registered and licensed to recruit in the UK, Switzerland, Mainland Europe and the Americas - we have offices in both the UK and Switzerland. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory, Clinical and Medical Affairs.

We match professional candidates to the best permanent, contract and interim roles in the market and for more information about our company visit us at www.advregulatory.com.

If you wish to apply for this role please click Apply Now, or send your CV with a covering note to CV@AdvRegulatory.com. Alternatively to have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the UK London office, on +44 (0)20 7801 3380.

Keywords / Key words: Medical, Medical Affairs, MA, Medical jobs, MA jobs, Medical Affairs jobs, Clinical Research, Clinical, Clinical jobs, Clinical Development, Project Management, Physician

To Apply : Please send a full CV in confidence to cv@advregulatory.com.

Contact Information:

Address:  Head Office
Head Office Suite 8 Penhurst House 352-356 Battersea Park Road London
SW11 3BY
England
Tel:  +44 (0)20 7801 3388
Website:  Visit Our Web Site

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