Job Details 
Phlexglobal
Our database has identified the following jobs as matching your search criteria. If you cannot see a job you are interested in, please search again refining your criteria or email us for further help and support.| Title | Clinical Research Associate (Germany) | ||
|---|---|---|---|
| Role | Clinical Research Associate | Reference | RF10798 |
| Location | Germany | Working hours | Full-time |
| Salary | On application | Employment type | Contract / Interim |
| Summary | Are you experienced with Trial Master Files and well practiced in performing Trial Master File reviews? Phlexglobal are looking to recruit a number of Clinical Trial Administrators and Clinical Research Associates, on short term contracts, to assist with an ongoing project in Germany. Successful applicants would form part of the innovative Clinical Task Force team. This project is all expenses paid by Phlexglobal with travel arrangements being taken care of on your behalf. Phlexglobal will provide all necessary project specific training. This is a great opportunity to get exposure of working in a European Pharmaceutical environment! | ||
| Description | Phlexglobal have a number of Trial Master Files to review on behalf of our Pharmaceutical client, over a 6 month period. We are looking to recruit between 4-5 additional people to join the existing team which is led by an experienced Phlexglobal Project Manager. Phlexglobal need commitment for a minimum of 12 consecutive weeks with start dates in August, September and October being acceptable for the right candidates. The role will involve a systematic review of a number of Trial Master Files on behalf of our client. You will need: • to be able to demonstrate a solid understanding of the Clinical Trial process, including knowledge of the EU Directive and the consequence of non compliance • to be proficient with all aspects of Trial Master Files • a solid understanding of the importance and significance of clinical trial documentation • experience of working with large multi-centre studies, in multiple countries, ideally across Europe. The role will involve working in a close team and with challenging timelines, so the ability to work under pressure and manage your time well is key. You would not need to speak German as all communications are managed in English, you will however, need to have a high level of both written and verbal English. All travel arrangements are co-ordinated on your behalf by the department administrator, and paid for by Phlexglobal so you would not be out of pocket. A generous daily allowance is allocated to cover sustenance. Telephone cards are even provided to ensure you can keep in touch with loved ones. The current team travel out from the UK to Germany on Monday, and then travel back on Friday each week, there is the flexibility to stay on in Germany if you wanted to be permanently based there for the duration of the project. Long weekends have also been factored into the 22 week duration to give some respite from the weekly travel. This is an opportunity to take on an exciting short term project which will take your current knowledge base to the next level for Trial Master Files, and ensuring legislative compliance, which is of upmost importance to us all whilst working in Clinical Research. Candidates must be eligible to work in the UK and be able to travel to/from Germany. | ||
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