Regulatory affairs specialists are in constant demand throughout the life sciences industry, whether for trialing new drugs and devices, bringing them to market or maintaining their licenses.
We specialise in matching professionals with specific experience and skill sets to our clients’ regulatory requirements. Our dedicated RA team works across the pharmaceutical, biotech and medical devices sectors, providing specialist staff for clinical trial applications, marketing applications (MRP, DCP, CP) through to life cycle management, CMC, labelling and artwork, regulatory operations, CE marking and 510K.
Many of our clients work with us exclusively, allowing us to offer you the best regulatory affairs opportunities that won’t be available elsewhere.
Contact us for your next career move, roles we specialise in include: