Regulatory Affairs
Warman O’Brien works with global pharma, biotech and SME clients to place talented Regulatory Affairs professionals
Recruiting Regulatory Affairs Talent
With the legislation surrounding pharmaceutical products and medical devices being in a constant state of flux, the role of the Regulatory Affairs professional has become increasingly crucial.
Warman O’Brien has built a strong understanding of the needs of the biopharmaceutical and medical devices market. We can support candidates and clients in filling roles at all levels of the regulatory affairs field: from regulatory affairs officers to senior regulatory affairs managers, our expert recruitment consultants can assist you with filling these roles on a permanent or contract basis.
Federal Regulations Affecting Clinical Data in the US
Organisation-critical regulatory affairs roles
Regulatory affairs jobs often span the life sciences sector, from in-house regulatory affairs officers working within global medical device manufacturers to chemistry, manufacturing and controls teams. Regulatory affairs professionals placed by Warman O’Brien have been consulting biopharmaceutical firms in emerging markets such as the Middle East and Asia-Pacific. We’re experts in ensuring passionate and dedicated Regulatory Affairs professionals fill these critical roles.
CMC
Chemistry, manufacturing and controls within regulatory affairs require a candidate with a multidisciplinary scientific background. With their teams alongside technologists and engineers, those in CMC jobs call for hands-on experience with a wide range of biological, physiological and chemical analyses, an understanding of statistics, scientific writing skills and a proven record in collaborative environments.
Regulatory Affairs Management
The role of the Regulatory Affairs Manager is to support and motivate their team, whether in-house or on a consultancy basis, in submitting regulatory documentation on new or existing drugs and medical devices. In addition, they ensure compliance with national and international legislations and ethical guidelines set by regulatory bodies such as the Medicines and Healthcare Products Regulatory Agency (MHRA) or the United States FDA.
Medical Writing
Medical Writers facilitate the development of marketing and advice on new medicines or devices for medical and healthcare professionals such as GPs. Our team is experienced in supporting candidates and clients in filling roles for these critical jobs. Also Medical Writers will often find themselves part of a wider medical communications agency, providing public and private sector services on legal and regulatory documentation and education.
Case Studies
At Warman O’Brien, we’re pleased to support the operations and clinical research needs of contract research organisations and leading biotech and pharmaceutical organisations across the globe.
To learn more about our experience sourcing executive talent for clinical operations, please see our recent case studies, where we explore the complex requirements needed to secure talented candidates for niche roles in this field.
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