Freelance Site Start Up & Regulatory Specialist Nr ref.: /JOBS.pl Freelance Site Start Up & Regulatory Specialist Job type: 9 month contract Location: Home based, with some travel to sites across Italy Hourly rate: Up to €85 per hour depending on experience Do you want to work for a world leading CRO in their Study Start Up team? Want to cover a variety of therapy areas at all stages of clinical trials? Interested in a role that will involve travel? A world leading clinical research organisation have recently released to us a contract position as a Site SU & Regulatory Specialist for a period of 9 months. You will cover a variety of therapeutic areas and phases, working in a fast paced environment. Key tasks: Reviewing essential document packages for site activation Preparing and submitting of packages to Central Ethics Committees and Local Ethics Committees. Competent Authorities and other Regulatory Bodies Reviewing Informed Consent forms Key requirements: 3-5 years' experience in submissions Experience in preparing and submitting to packages to Competent Authorities, Central and Local Ethics Committees Strong experience in country specific (Italy) submissions Proven ability to work unsupervised Fluent English Remember if this role is not suitable for you or you are no longer looking for a new job please feel free to forward this to anyone you feel would be suitable. If we successfully find a role for your recommendation we will give you £250 in vouchers of your choice. Key words: Regulatory, Regulatory Affairs, SSU, Study Start Up, Site Activation, Site Start Up Specialist, Regulatory Affairs specialist Clinical, CTA, Ethics Committee, Milan, Italy, home working, Competent Authorities, Site Activation, Clinical Operations, Clinical Research, Informed Consent Forms Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .
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