An outstanding opportunity to join one of the worldâ€™s leading contract research organisations and be part of a dynamic and growing international company. Join PRA as a Regulatory Affairs Associate and help realize your career potential.
JustPharma are assisting in the search for Regulatory Affairs professionals for an opportunity as an Associate or as a Senior Associate. The position is working with a large company in the Pharmaceutical industry and are offering the role to be office based close to Reading, or fully based from home for experienced candidates.
Regulatory Affairs Senior Associate
Are you seeking to take the next step up in your career within global regulatory submissions and publishing? If so, I have the perfect role for you! A vacancy has arisen with a reputable regulatory consultancy firm based in Berkshire, seeking a Senior Associate to come aboard. Berkshire Maidenhead Windsor Slough Reading
As Senior Regulatory Affairs Associate, responsibility will be covering lifecycle activity within the EU, Emerging and African regions for a blockbuster product and other specialist therapy areas. Including; the preparation, submission and review of CTAs, MAAs, IMPD, PIPs. This role will suit a candidate with relevant experience looking for an organisation to develop within.
Regulatory Associate/Officer â€“ Health and Personal Care
Â£35,000 - Â£40,000
Our client is one of the largest OTC pharmaceutical companies in the UK and due to pipeline there are recruiting for a Regulatory Officer/Associate to based from their offices in Berkshire.
Regulatory Affairs Manager of Consulting
Are you seeking to take the next step up in your career within Regulatory Consulting? If so, I have the perfect role for you! A vacancy has arisen with a reputable regulatory consultancy firm based in Berkshire, seeking a Manager of Consulting to come aboard. This role requires 50% international travel.
The role of Regulatory Affairs Manager is responsible for planning regulatory submissions, mentoring and supervising a team for provision and maintenance of core dossiers and co-ordination of labelling activities. Through leading cross functional project teams, youâ€™ll ensure preparation of high quality documentation for all regulatory submissions, both medicinal products and devices, whilst building relations with Reg bodies in order to expedite approval.
Associate Director Regulatory Policy and Intelligence opportunity has arisen with a leading Research based Biotherapeutics Company in the South East on a permanent basis with an excellent salary and benefits package on offer. This is a highly visible role with regular liaison with internal cross-functional departments and external Regulatory Agencies and associations.
Opportunity for an experienced Emerging Market Regulatory Affairs Manager to join this global Pharma Company on a permanent basis. Remit includes line managing 2 Senior Regulatory Associates, ensuring effective strategic input to Global Regulatory Plans, and that teams / functional groups are provided with clear, constructive regulatory input to assist planning and issue resolution across lifecycle activity. Excellent promotional / development opportunities.
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