| Clinical Trials Assistant /Co-ordinator (CTA/CTC) Reading GBP26K Are you a well organised person?
Do you want to be involved with interesting fast paced clinical trials?
Do you want to work for a company that truly believes in supporting and developing staff?
This could be an excellent opportunity for you:
This is an office based position in Reading. Ideally you will have 12-18months prior experience in a similar position. You will be joining an excellent team of three Clinical Trials Assistants/Associates. Please call Zoe Benningfield on # 469 # You will:
Ensure that study related work are up to date, complete and readily available to team members. Ensure adherence to protocols and quality of information received, in line with UK & EU regulations, GCP guidelines and company SOP s Facilitating regulatory submissions and ethics committee applications ( e.g. copying and filing regulatory documents and providing administrative support), as necessary Tracking of Ethics/Regulatory submissions. The efficient and accurate administrative processing of forms concerning data collection, payments and other materials with regard to clinical trials. Activities are based on the guidelines as described in company SOPs Be an internal focal point for Clinical Team, ensuring appropriate dissemination of information to team members Communicate with all relevant internal and external contacts on a professional level: provide adequate information, consult the appropriate persons in case of problems and make a positive contribution to the decision making process. Co-ordination of investigator meetings and related activities, as necessary Track study related documents Participate in Study Team meetings and write/collate/distribute minutes for study team meetings Update and maintain electronic and hardcopy versions of the study TMF by filing and tracking clinical documents.
To hear more about this position please call Zoë Benningfield on # 469 #
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