Parkside recruitment are pleased to be recruiting a Clinical Trials Administrator for our client within the Pharmaceutical sector with a document management background to organise, maintain and complete Administration supporting clinical operations project managers on day-to-day study management activities and clinical operations functions ensuring they are supported in order to assist in the delivery of Clinical Development objectives and achieve clinical excellence. You will have: Substantial administrative experience or qualified to degree level. Scientific background is essential.Experience or knowledge of regulatory documents or medical terminology is essentialExperience in clinical operations area related work is essential.Must have working knowledge of computer applications including Microsoft project.Must be organised and detailed-oriented.Able to produce work of high quality in a timely manner.Up-to-date Good Clinical-research Practice training. Main Responsibilities:Organise, maintain and complete the paper and electronic trial master files, including collation of study documents from monitors, appropriate filing of documents.Identify, request and ensure delivery of outstanding and outdated documents.Periodically, and at the end of the study, review study files / folders for organisation and completeness.Assist in setting up clinical study files / folders at study sites and assist in quality review of the study site files / folders throughout the study.Assisting by offering support for day-to-day study management activitiesTracking the distribution of protocols and protocol amendments.Creating drafts of study-specific documents.Seeking signatures for approved documents.Conducting in-house clinical operations functions, including clinical supplies coordinationAssisting the investigator meeting preparation and coordination, document processing and study status tracking.Arranging and minuting Study Team Meetings (as required) and completing actions as necessary.Assist in the project management and monitoring of clinical studies, including liaison with study sites, monitors, drug vendors, central laboratories and other vendors for study related tasks.Perform various study related functions as required and assigned to ensure the accurate, quality, timely and on budget execution of clinical studies, to include:Maintaining budget tracking tools as appropriate.Parkside Recruitment Ltd is acting as an Employment Agency in relation to this vacancy. Parkside Recruitment is an Equal Opportunities Employer.
Compania este în topul firmelor care se pot confrunta cu mult succes cu prezentul și cu viitorul, așadar caută în prezent un manager de resurse umane care să ofere contribuții strategice și să execute strategia și agenda optimă a capitalului de talente.