Company: RBW Consulting
Closing Date: 23 Oct 16
Salary (£): Negotiable
I am currently seeking an experienced freelance CRA for a monitoring role based in Japan.
Working for an expanding consultancy, the successful candidate will be responsible for all aspects of study site monitoring, from study start-up to close-out, working on an exciting portfolio of studies. From regular contact with Investigators, vendors, and trial sites, you will ensure the integrity of clinical data and ensure that clinical trials are in accordance with SOPs, ICH-GCP, and relevant local and international regulatory guidelines. You may participate in study development and start-up processes, and will be responsible for multiple projects, both working independently and in a team environment.
The ideal candidate will have:
This is one of several positions I am currently recruiting for so do please get in touch for a confidential discussion around your current situation and what your ideal next move would be. Please contact Adrienne Watkin on +44 1293 584 300 or email a CV to firstname.lastname@example.org
Clinical Research Associate | Senior CRA | clinical trials | SCRA | CRA II | clinical trials | clinical research | clinical | pharmaceutical | CRO | clinical trials | monitoring | Japan | Tokyo
Origin Two 106 High Street, Crawley RH10 1BF
|Tel:||01293 584 300|
|Fax:||01293 534 133|
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