Regulatory and Start Up Specialist (Portuguese speaker)
Precision Medicine Group EN
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In brief
Precision Medicine Group is hiring: Regulatory and Start Up Specialist (Portuguese speaker) in Spain.
Duties
- Essential functions of the job include but are not limited to: Responsible for delivery, in terms of timeliness and quality, of site activation…
- Responsible for/facilitates the translation and co-ordination of translations for documents.
Required profile
- Apart from the experience with regulatory submissions, for this role it's key for candidates to have contracts and budgeting negotiation experience…
- Preparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial and amendments/notifications) for submission…
- Partner with the assigned site CRA to ensure alignment in communication and secure site Review and manage collection of essential documents required…
- Act as SME for collection and maintenance of site level critical path to Site Activation data points, including but not limited to Competent…
Excerpt from the ad
Precision for Medicine is a global Clinical Research Organization with uniquely integrated offering which enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational…
Source: ad by Precision Medicine Group, published on Greenhouse. MakeYouFirst summarises this ad; the advertiser remains responsible for its content.