Regulatory

Clinical Professionals Regulatory Department specialises in the placement Regulatory Affairs jobs specialists throughout Europe. From Regulatory Affairs Executives to Senior Regulatory Consultants, we source opportunities for contract and permanent roles throughout all stages of the Regulatory Approval and Post Approval process.

Roles we source in this sector include:

Clinical Regulatory Affairs jobs consist of preparing and compiling Clinical Trial Applications (CTAs) post marketing activities such as management and maintenance of the drug products lifecycle and Marketing Authorization Applications (MAAs) among others. Therefore, experience in post marketing activities or clinical regulatory activities is highly valuable.

Clinical Professionals also work extensively with Regulatory Consultants. We offer a variety of jobs, from interim opportunities through to long term contracts working domestically or on an international basis, from 0.1 - 100% FTE. Clinical Professionals work with a broad range of organisations, from large blue-chip Pharmaceuticals through to start up consultancies allowing our consultants to provide expertise to an array of companies that focus on various therapeutic areas.

Regulatory Affairs jobs available include:

Regulatory Affairs Document Management Officer jobs
Head of Regulatory Affairs
Regulatory Project Manager jobs
Regulatory Operations Associate jobs
Regulatory Affairs Executive jobs
Regulatory Affairs Director jobs
Regulatory Consultant jobs
Regulatory Manager in Submissions Compliance jobs
Regulatory Affairs Administrator
Regulatory Affairs Manager
Regulatory Submissions Associate jobs
Regulatory Manager in Intelligence and Compliance jobs

Clinical Professionals Candidates

Candidates selected by Clinical Professionals are high calibre, and well-trained in relevant scientific disciplines. Our candidates have previously held positions at regulative authorities, regulative bodies or with Pharmaceutical, Biotechnology or similar organisations. Our candidates are experienced in a range of regulatory environments providing them with a comprehensive understanding of the clinical product lifecycle and local approval processes.

Clinical Professional Regulatory Consultants are trained specifically in this discipline in order to supply high quality, detailed advice regarding specific areas of expertise. We also offer expertise in the following areas, for which we have specialist Resource Teams:

Useful Links:

The Organisation for Professionals in Regulatory Affairs gives you the opportunity to attend regulatory affairs and symposiums courses as well as stay up to date with regulatory news worldwide and expand your network whilst advancing your career.

For more information on the latest Regulatory Affairs jobs from Clinical Professionals Contact us.