Senior Associate Study Management
Russell Oakley at CK Clinical is recruiting for Senior Associate Study Management to join a pharmaceutical company at their site based in Uxbridge or Cambridge on a contract basis. The role is with the Investigator Led Studies team and is for 12 months in the first instance.
Requirements: Ability to understand technical, scientific and medical information Understanding of drug development process Familiar with concepts of clinical research Advanced computer skills Experience in interactions with outside vendors, e.g., CROs and contract labs Experience with administration of site budgets and grants with supervision Experience with development of prospective site-selection criteria Experience with reviewing adequacy of site-proposed ICs for compliance with relevant regulations Detailed knowledge of Good Clinical Practices (GCP), FDA regulations and guidelines, and applicable international regulatory requirements Ability to write and present clearly using scientific and clinical issues terminology Experience dealing with time demands, incomplete information or unexpected events Good organizational and planning skills Experience working effectively in a team/matrix environment
For more information or to apply for this position, please contact Russell Oakley on 01246 45 77 33 or email email@example.com. Alternatively, please click on the link below to apply online now.
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL34505 in all correspondence.