AXESS has an in-depth knowledge and excellent track record of recruiting with regulatory affairs 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. These roles include Regulatory Development, Regulatory Operations, Regulatory Submissions (MAAs utilising National, Mutual Recognition, Decentralised and Centralised procedures) and marketed products. We also recruit CMC, publishing and project management specialists.
We are seeing an increasing demand for regulatory affairs professionals as our clients grow their teams in response to new compounds in pipeline and increasing regulatory challenges. We typically have positions available at all levels of seniority with the majority having EU or International scope. 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 providing 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 view article). Whether you are looking for your first move in your regulatory career, aspire to achieve your first managerial position and become more strategically focused or are keen to move from an EU to International position we are happy to offer objective career advice, detail the options available to you, provide market insight and work with you to secure the right role.