I am now recruiting for Clinical Trials Documents Specialist to join our drug development client in a permanent, full time position which can be field based within Scotland.
This is a really good opportunity to join an established, Pharmaceutical development company, where you will be providing key support to a range of interesting clinical trials, both early Phase and late Phase.
You will be joining a busy department that requires a focused individual with an eye for detail.
For this position, the ideal candidate will have experience of working in a clinical trials environment, using TMF (Trial Master Files) or eTMF systems, knowledge of ICH - GCP guidelines and be familiar with a range of clinical trials documentation and clinical trials procedures. You will be supporting new studies and legacy studies too.
Preparing files for internal or external audits and experience in overseeing documents and files shared for vendors / CROs will also be beneficial.
In addition to this, you should also be able to demonstrate excellent organisation skills and be able to work well in a team that works hard together to meet key deadlines.
Prior experience with working on different strategies towards the documentation of clinical files will be advantageous.
To learn more about this very interesting company, role and to discuss your career requirements, please get in touch to arrange a discussion with me, Simon Penrose, on 01293 584 300 or email firstname.lastname@example.org or hit apply.
Salary: On application
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