Clinical Research Trials Coordinator Location: AmershamDuration: 6 MonthsRate: CompetitiveClinical Research Trials Coordinator job opportunity based in Amersham for a global organisation, which provides transformational medical technologies and services to meet the demand for increased access, enhanced quality and more affordable healthcare around the world.As a Clinical Research Trials Coordinator, you will join a busy Operations Team to assist in managing the lifecycle of all supported Investigator Sponsored Trials. You will proactively manage all aspects of study-related support across all brands and review documentation to verify that all research operates within global/regional regulations and complies with guidelines.The successful Clinical Research Trials Coordinator candidate will have a background in clinical trials, research and governance. As a Clinical Research Trials Coordinator, you will have strong knowledge of clinical trial and research governance as well as the ability to multi-task and carry out tasks accurately and in a timely manner. Clinical Research Trials Coordinator Key Responsibilities:Support business objectives by facilitating trial review processesEffectively communicate the decisions by establishing follow-up meetings with key stakeholders.For approved studies assist the IST Responsible Person to ensure relevant workflows are processedReview supporting documentation for compliance and alignment to ISTC decisionsTrack progress against key milestones via organisational tools including databases, budget tracker, PUT Tool.Build and expand relationships with internal and external customersReview invoices for alignment to milestones and obtain proof of milestone achievement.Review workflows relating to milestone funding and product supply for accuracyManage information requests from internal and external customersContinuously monitor Mailbox and FOC (free-of-charge) confirmations mailbox and respond to queries and issues received. Clinical Research Trials Coordinator Candidate Criteria:Strong coordination, administration and customer service experienceClinical / Pharmaceutical trial and research backgroundAbility to discuss good clinical practice guidelinesInvoicing experienceMS Office experience including PowerPoint, Word and ExcelAttention to details along with the ability to multi-taskPlease submit your CV in the first instance or call Emma Jones on 07483128595.