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Resourcing Solutions for Medical Affairs, Regulatory Affairs and Clinical Development
AXESS has an in depth knowledge and significant expertise within Regulatory recruitment across Europe and the Emerging Markets. Specialist consultants work with a wide range of pharmaceutical companies, recruiting permanent and interim professionals for a broad range of regulatory roles, which encompass the whole regulatory lifecycle including Regulatory Development, Regulatory Operations, Regulatory Submissions (utilising National, Mutual Recognition, Decentralised and Centralised procedures) and marketed products. We are often called in early by clients to advise on structure, remuneration packages and individual role profiles, before then going on to fill these roles.
We have an excellent reputation for giving tailored advice to candidates on entry to the industry or those looking to develop their career paths. Our expertise has been recognised externally and we have contributed to The TOPRA Guide to Careers in Regulatory Affairs (click in the image to the right to view article) and one of our consultants is a Lecturer on the MSc in Regulatory Affairs offered by TOPRA which is validated by the University of Wales.
Permanent office based position for an experienced Regulatory Affairs Associate Director to join the team at this respected Global Pharmaceutical Company. The offices are based in Central London.
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Permanent position for a CMC Project Manager to work within this renowned Global Pharmaceutical Company. Responsibilities include: product registration, submissions, representing Regulatory cross functionally, coordinate affiliates and ensuring compliance across life cycle. The role has strategic elements and will see you mentor and train team members.
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Opportunity to join this specialist medical systems company in this brand new role, as Quality and Regulatory Affairs Manager.
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Great opportunity for an experienced Regulatory Affairs Consultant looking for 2 – 3 days/week over 6 months. You will have the ability to add immediate value within a busy Oncology team. Strong EU regulatory experience and a good understanding of US regulatory processes essential. Limited Company Contractors welcome to apply
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Our client has two urgent vacancies within their Regulatory Affairs Department. You will be immediately available and able to take on responsibility for clinical trial submissions, scientific advice, and regulatory input into clinical and drug development plans. You will also manage MAA submissions for compounds allocated as well as assisting with new pipeline projects and late stage candidates brought in through in-licensing. 6 month contract – either 5 days or 3 days/week.
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As Regulatory Affairs Manager you’ll be responsible for planning and managing all regulatory activity associated with a UK and Ireland product portfolio. This small Pharmaceutical Company offers a fantastic working environment and is based just West of London.
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As Associate Director Regulatory Affairs, you’ll lead the Regulatory Development strategy for the EU on two Global Diabetes (Endocrinology) products. You’ll plan, manage and execute regulatory activities liaising with global regulatory leadership whilst ensuring regional regulatory therapeutic area strategic guidance is adhered to on development projects and marketed products, including a Top 10 global product.
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Opportunity for an experienced and responsible Regulatory professional to join this dedicated Reg Team to collate documents and prepare Marketing Authorisation Applications. You’ll also co-ordinate cross-functional teams to prepare responses to questions from authorities.
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The Associate Director Regulatory Affairs, at Allergan, is responsible for strategic regulatory input into Global Development Plans and subsequent implementation, to ensure the registration of commercially successful products (Class IIb and Class 3 Medical Devices) in the EU and Emerging Markets Region. This role carries line management responsibility
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