Job Overview

Apply now We specialise in the recruitment of high quality candidates with expertise in Clinical and Regulatory Documentation. We have an excellent opportunity for an Administrator to join a global biotechnology / pharma company based in Cambridge. Core Duties The provision of administrative support for the company's regulatory documentation management and for internal and external staff and company contracted clinical research organisations. Key skills and knowledge Understanding of global regulatory requirements and guidelines for conducting clinical trial and clinical research.Knowledge of relevant GCP, external and internal regulatory requirements/guidelinesProject Management/planning experienceAbility to collaborate and build relationships to maximize organizational function and capabilities Qualifications Required Masters Degree ORBachelor's Degree & 2 years directly related experienceAssociates Degree & 5 years of directly related experienceHigh School diploma / GED & 8 years of directly related experience Desirable Qualifications: BS/BA/BSe in the sciences or RN2 years Clinical Documentation Management and industry experience (e.g. CTA/CRA/Study Manager) in order to have a thorough understanding of the processes associated with the conduct of clinical trials and document management operations. Are you enthusiastic about this job? Send us your CV in word format today

Key Requirements

Clinical Research Document Management Regulatory Requirements Degrees Administration