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Sandrine Rosso is listed as Consultante à PharMarketing GDPR lifescience at PharMarketing, based in Greater Nice Metropolitan Area, France. AeroLeads shows a work email signal at free.fr and a matched LinkedIn profile for Sandrine Rosso.
Sandrine Rosso previously worked as Freelance recherche clinique, audit BPC, anonymisation données cliniques et soutien en RGPD at Freelance and Gestionnaire d'étude Clinique at Galderma, Sophia Antipolis. Sandrine Rosso holds Certification, Rgpd Et Protection Des Données Personelles from Impact Rgpd.
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Management d'études Cliniques de CROs et Monitoring; Anonymisation des documents cliniques (selon EMA policy/0070) Qualité: Organisation de système Qualité et procédures et Réalisation d'audit BPCRGPD vérification et support pour le respect de la protection des données personnelles
Listed skills include Cro, Fda, Protocol, Crf Design, and 3 others.
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Protection des données personnelles: support pour la vérification de la mise en place et du respect du RGPD, DPO externe
Biot, France
Management d’étude clinique et étude épidémiologique o Suivi des études cliniques internationales DM, médicaments et non-interventionnelle et Management des CROso Rédaction/revue de protocole, CRF/eCRF, information et consentement patients, documents patients, et documents d’étude (CRF guideline, Plan de monitoring, Trial Master file…),o Vérification de contenus/qualité de TMF.o Monitoring des sites d’investigation (sur site ou en remote)o Revue des rapports de monitoring, suivi et management des actions.Système de management de la Qualité o Revue de processus et rédaction de SOPs,o Audit BPC : préparation, conduite et suivi,Anonymisation des données cliniques selon l'EMA policy/0070Vérification ou support pour le respect du RGPD/Protection des données personnelles
Sophia Antipolis
Specific mission of :-Set-up of clinical studies including Ethics Committee submission files preparation.-Quality control of TMF before long term archiving
CRO management and study follow-up.Quality Assurance activities for Clinical Research.Organisation/set-up and follow-up of processes linked to clinical research activities.Preparation and answers to the report of the FDA and EMA joint Inspection.
Monitoring of Phase I and II studies in Europe.Set-up of secondary monitoring process for Phase I/II studies.Set-up and organisation of clinical studies archiving activities.
Management of Trial Master Files for clinical studies managed by the CRO.
Activities and Societies: Support pour la vérification du respect du RGPD au sein de TPE/PME
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Sandrine Rosso works for PharMarketing.
Sandrine Rosso is listed as Consultante à PharMarketing GDPR lifescience at PharMarketing.
AeroLeads has found 1 work email signal at @free.fr for Sandrine Rosso at PharMarketing.
Sandrine Rosso is based in Greater Nice Metropolitan Area, France while working with PharMarketing.
Sandrine Rosso has worked for Pharmarketing, Freelance, Galderma, Sophia Antipolis, Nicox, Sophia Antipolis, and Fdm Pharma, Sophia Antipolis.
You can use AeroLeads to view verified contact signals for Sandrine Rosso at PharMarketing, including work email, phone, and LinkedIn data when available.
Sandrine Rosso holds Certification, Rgpd Et Protection Des Données Personelles from Impact Rgpd.
Sandrine Rosso is listed with skills including Cro, Fda, Protocol, Crf Design, Ctms, Clinical Development, and Medical Writing.
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