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| Job Location | Cambridge |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Contract, full-time |
CK Group are recruiting for an Evidence Delivery Associate Director to join a company in the Pharmaceutical industry at their site based in Saffron Walden on a contract basis for 12 months and has a daily rate of £650 LTD.The Company:Our client is a global pharmaceutical company with a major presence in the UK. Their purpose is to deliver life-changing medicines and to do this they are completely science-led and like to share this with the scientific, healthcare and business communities within the UK.The Location:The role is based at our clients site in Cambridge, a town famous for its history, university and architecture. There is also the added benefit of being accessible to London as well as Stanstead and Luton airports. The Role:The successful candidate will:- Lead 1-3 multi-disciplinary multi-national study delivery teams in the Oncology arena. - Deliver studies to agreed timelines (scorecard), within the approved budget and according to quality standards. - Ensure global oversight over the operational study start up, implementation and closure and ensure inspection readiness.- Lead study related change management within business strategy, s.a. assessment of scope changes. - Ensure Compliance with Procedural Documents, Standards and Policies, international guidelines and local regulations at any time, and report compliance breaches.- Undertake feasibility assessments with internal and external stakeholders.- Manage study system reporting.- Lead the study and manage the study team stakeholders.Your Background:- Prior experience leading & project managing a multi-disciplinary, multi-national virtual teams responsible for the delivery of multi-national, multi-site clinical (or evidence generating) trials.- Prior hands-on experience in clinical research (or evidence generation) activities in total (which may include project managing a single country with multiple participating sites and monitoring of those sites).- Experience in the Oncology Therapy area, ideally in a project managerial roles looking after multi-national clinical trials or evidence generation trials. - Proven project management expertise. - Very good knowledge of the aspects of the Clinical Study Delivery process, international ICH/GCP guidelines and the Drug Development industry. - Good medical knowledge in Oncology.Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.CK Group 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 47549 in all correspondence.