Latest Executive Jobs 130

Contractor, Regulatory Labelling
Uxbridge
6 Month Contract
ÂŁ70 - ÂŁ90 per hour

You will be acting as a Quality Assurance Specialist for a globally successful pharmaceutical company, Your main responsibilities will include the administration and development of databases and spreadsheets, you will help support the company in their goals of continuous improvement and and you will manage the quality data compliance and coordinate management review process for Europe.

My client an innovative pharmaceutical company with an impressive development pipeline currently has an opening for a Senior Clinical Pharmacologist to join their growing Clinical Pharmacology division.

Join one of the world’s finest Pharmaceutical companies as a Director of Global Regulatory Affairs. This role reports directly into the VP of European Regulatory Affairs and comes with direct reports full project responsibility for Centralised Fillings and Scientific advice. Contact Theo Moore for full details on 0207 801 3384 or email us (in confidence) at Cv@advregulatory.com

A multinational organisation who specialise in patient focussed therapies are looking to recruit a new Head of Quality Assurance for their UK Manufacturing facility in South Wales.

Please call Matt Greig on +44 (0)207 801 3382 or direct on +44 (0)7918 679 405 (eves / weekends). Alternatively you can email me on Matt.Greig@AdvRegulatory.com

Job Summary:
Provide advanced level of SAS programming activities for the monitoring, reporting, and analysis of clinical trials and will deliver against the overall protocol timelines and quality goals within the study teams.

For a confidential consultation call Russell Gillam on 0044 (0) 207 255 6665 or email your CV to russell.gillam@secpharma.com

My client is an expanding Biopharmaceutical in a critical stage of development. They have an enviable pipeline of small and large molecules and already have in place a strong management team. Your role will be to lead a team on Global development, filing and brand extension projects on key indications. This is a high profile visible role which will suit a true regulatory performer. Contact Theo Moore on +44 (0)207 801 3384

To apply for this Head of Regulatory Affairs role please call Julie Cooper on 020 8305 9733 or 07951 082482

Alternatively please send your CV to:

julie@mosaicrecruitment.co.uk

An outstanding opportunity at one of the world’s top Contract Research Organisations (CRO) has become available. As part of an organisation that delivers global clinical drug development to pharmaceutical and biotechnology companies, you will have senior responsibility that will be crucial to advancing the department and company. There are excellent career progression opportunities within this organisation. This is an office based position in Manheim, Germany.

OPTION FRANCAIS *** Regulatory Managers for CMC Bio *** Work on global submissions for BLAs and MAAs ... Please call one of Advanced Regulatory’s Principals for Regulatory Affairs, Theo Moore on +44 (0)207 801 3384 or +44 (0)7918 195 166.

My client is currently recruiting for an Associate Director for Clinical Development, working within the G.I therapy area. You will responsible for both medical direction and clinical strategy for the assigned projects amongst a number of other duties. My client is a pharmaceutical company based in Middlesex.

Senior Regulatory Affairs Officer CMC

Senior Regulatory Affairs Officer CMC is a diverse role within this global pharma development company. You will be a part of the international regulatory cmc team and will have responsibilities for preparation and submission of CMC regulatory documents for investigational/development products and existing commercialised products. This will involve a lot of cross functional communication with therapeutic regulatory, quality and development teams.

This is a fantastic opportunity for a senior pharmacovigilance (PV) physician to join one of the worlds’ leading pharmaceuticals as part of their Global PV team. Based in the Frankfurt area, your role will be to focus on the risk management of international compounds to include signal recognition, risk assessment and strategy.

This is a fantastic opportunity for a senior pharmacovigilance (PV) physician to join one of the worlds’ leading pharmaceuticals as part of their Global PV team. Based in the Frankfurt area, your role will be to focus on the risk management of international compounds to include signal recognition, risk assessment and strategy.