Regulatory / SSU
il y a 1 mois
Role: Regulatory and Study Start Up Length: 4 Months
Location: France
reparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial and amendments/notifications) for submission to CA, EC, and other applicable local bodies according to local requirements and within required timelines to obtain all necessary authorizations/approvals for the conduct of the Clinical Trial according to international and local/national applicable regulations, company SOPs and principles of ICH-GCP.
Please click ‘apply’ or contact Mona Azhari (Senior Recruiter) at Planet Pharma for more information:
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Regulatory / SSU
il y a 1 mois
France Planet Pharma Temps pleinRole: Regulatory and Study Start Up Length: 4 Months Location: France Role Overview: Responsible for delivery, in terms of timeliness and quality, of site activation readiness within the assigned country/sites and foreseeing and mitigating any risks. Requirements: reparation of Clinical Trial Application Forms as well as preparation of submission...
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Regulatory / SSU
il y a 1 mois
France Planet Pharma Temps pleinRole: Regulatory and Study Start Up Length: 4 Months Location: France Role Overview: Responsible for delivery, in terms of timeliness and quality, of site activation readiness within the assigned country/sites and foreseeing and mitigating any risks. Requirements: reparation of Clinical Trial Application Forms as well as preparation of submission...
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Regulatory / SSU
il y a 1 mois
France, FR Planet Pharma Temps pleinRole: Regulatory and Study Start UpLength: 4 MonthsLocation: FranceRole Overview:Responsible for delivery, in terms of timeliness and quality, of site activation readiness within the assigned country/sites and foreseeing and mitigating any risks.Requirements:reparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial...
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Regulatory / SSU
il y a 1 mois
France Planet Pharma Temps pleinRole: Regulatory and Study Start UpLength: 4 MonthsLocation: FranceRole Overview:Responsible for delivery, in terms of timeliness and quality, of site activation readiness within the assigned country/sites and foreseeing and mitigating any risks.Requirements:reparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial...