Clinical Trial Manager

Job Description

Clinical Trial Manager6 Months £18.93 - £22.87 per hour Work Location: Remote Advantage Resourcing are currently working with an established University in the heart of London who are seeking a Clinical Trial Manager on an initial 6 Month Contract. We are looking for someone who will manage the coordination of the clinical trials in collaboration with scientists. You will be interacting closely with the Statisticians, Clinical project managers, Project leads, Data Managers, Data scientist, programmers and Trials assistants as part of the Trial team. You will also be responsible for the day to day co-ordination of their clinical study/ies, working with the other members of the team and the sites to ensure the successful delivery of the study. The main duties of the post include training the site staff on the trial procedures, writing documentation, monitoring the data and ensuring that all regulatory requirements are met in a timely manner.Core duties:- Producing trial documentation according to scientific requirements of the protocol and in line with the regulations and Units guidelines for data collection and management.- Promoting trials to ensure wide participation and good accrual of patients. This will include assisting in the production of newsletters, visit sites, attendance at scientific conferences and meetings and presenting information about the trials.- Assist with developing programmes, agendas for regular team meetings and possibly national and International meetings.- Provide training, information and advice to Trial Clinicians, Research Nurses and Pharmacists on all protocol requirements.- Take responsibility for the on-site monitoring of the clinical sites , where necessary , to ensure that sites are following the protocol and Good Clinical Practice (GCP) guidelines- Coordinate the purchasing, delivery and coordination of the trial drug supplies and site accountability processes are in place and being followed if required.- Preparation and presentation of written and oral reports to the TMG, TSC or other groups and/or at scientific meetingsEssentials for this role:- Good level of scientific understanding to degree level or through equivalent experience- Previous experience or knowledge of coordinating multi centred International clinical trials in Cancer/HIV or Tuberculosis trials - Recent experience in the conduct of clinical trials involving Investigational Medicinal Products (IMP) and safety management and reporting - Good working evidence of implementing GCP- Experience of study trial document development including protocols, CRFS, manuscripts, study reports and Standard Operating Procedures.- Understanding of Clinical trials methodology and stages in the testing of new products and other interventions, and an excellent knowledge of current regulatory requirements governing clinical trials including a practical understanding of GCP.- Understanding of the regulations and governance environment for Clinical research in the UK.Please apply if you feel you have the correct skill set/experience. Advantage Resourcing is a service driven recruitment consultancy. Required skills

GCP

IMP

clinical trials

clinical trial manager

Investigational Medicinal Products

monitoring data

trial procedures

trial documentation

trial promotion

Cancer/HIV trial

Tuberculosis trials

Keyskills :
GCP IMP clinical trials clinical trial manager Investigational Medicinal Products moniting data trial procedures trial documentation trial promotion Cancer/HIV trial Tuberculosis trials