| Description: | Here is a challenging European project management role within a large pharmaceutical company! We are looking for two study managers to take on phase II and III studies in oncology and gynaecology. You will work part home, part office based and will form part of a global programme team. When you work as a study manager at this company you are responsible for managing all activities from planning the study and writing the protocol through to the production of the study report. Studies are run through CROs so you will be managing the relationship and monitoring performance on an ongoing basis, in addition to leading the internal team and managing budgets/timelines. You will also play a key role in the start up of new projects which will get you involved in study design, outsourcing decisions, patient recruitment strategy and resourcing. Who should apply? Ideally you will be working at study management level within either CRO or pharma, although applications will be considered from strong lead CRAs with experience of co-ordinating studies across Europe. Previous experience with oncology or gynaecology trials is desirable. You will be comfortable working with various IT systems and happy to work independently with minimal supervision. Your experience will be rewarded with a competitive remuneration package, excellent training and the chance to work for a large blue chip pharmaceutical company with an excellent reputation for delivering blockbuster drugs! Call now for more information! |
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