Cours d'anglais gratuitsRecevoir 1 leçon gratuite chaque semaine // Créer un test
Connectez-vous !

Cliquez ici pour vous connecter
Nouveau compte
Des millions de comptes créés.

100% gratuit !
[Avantages]


Comme des milliers de personnes, recevez gratuitement chaque semaine une leçon d'anglais !



- Accueil
- Aide/Contact
- Accès rapides
- Lire cet extrait
- Livre d'or
- Nouveautés
- Plan du site
- Presse
- Recommander
- Signaler un bug
- Traduire cet extrait
- Webmasters
- Lien sur votre site



> Nos sites :
-Jeux gratuits
-Nos autres sites
   


Correction/ resume

<< Thèmes généraux, jeux, chansons || En bas

[POSTER UNE NOUVELLE REPONSE] [Suivre ce sujet]


Correction/ resume
Message de fouz94 posté le 22-08-2010 à 08:01:05 (S | E | F)

BONJOUR,

J'aurai encore besoin de votre aide précieuse pour mon CV!
MERCI BEAUCOUP!

Clinical Data Manager/ Programmer
PROFILE
Clinical Data Management professional with experience managing CDM responsibilities within Oracle Clinical, Inform, Clintrial and SAS Systems, developing/maintaining global data standards, CDISC/STDM mapping, validation/edit check programming, ad hoc reporting, editing/querying clinical data for consistency and accuracy, medical coding, management of clinical studies from data-base set-up to data-base lock ,developing/maintaining internal documentation, specifications and processes. Create/deliver departmental training and ongoing mentoring. Involvement in validation and quality control of new/updated application systems
Career Objective: To obtain an international position in Clinical Data Management using my French and English skills to bridge gap between the two cultures.

Technical Experience
Programming knowledge and familiarity in SQL, PL/SQL, SAS
ecrf sofware : ORACLE Clinical V4.03/ V4.5, INFORM, CLINTRIAL 4.03
Software: ACCESS, ENTRY POINT, SYMETRYC, DATA WAREHOUSE
Proficient in Microsoft Windows; Microsoft Office
Extensive working knowledge of CDISC/SDTM standards


PROFESSIONAL EXPERIENCE
2001 - Present
xxxxx Company (Lxxxxx, France), Contractor in clinical research activities.
I worked at the following companies via this Contract Research Organization:

Since January 2010 
xxxxx Company (Uxxxxx, France) as Business Administrator under SAS Data Warehouse and Inform (ecrf)
• Administrate Ipsen standard data model in consistency with drug development operational objective and timelines
• Ensure clinical studies are compliant with the standard (standard (e) CRF pages/forms, external data process)
• Develop/maintain global data standards, CDISC/STDM
• Take part in the solution of problems send to Data warehouse group
• Create/deliver departmental training and ongoing mentoring
• validation and quality control of new/updated application systems
• Create and maintain the documentation: user guide, guideline, database structure specification, CRF completion guideline...
• Review the study protocols and the draft of (e)CRF/CRF
• Review and validate the study database specification
• Perform the testing/UAT for (e)CRF screens, database structure, data loading, etc…

April 2001-december 2009
xxxxx company (Cxxxxx, France)

Study database support group, April 2007 – December 2009
as Database Designer under Clintrial V4 and ORACLE Clinical (RDC)
• Design databases for clinical studies (setup).
• Edit Check Programming according to “Data Validation Plans” for several studies
• Ensure clinical studies are compliant with the standard (standard (e) CRF pages/forms, external data process)
• Take part in the solution of problems send to Database group
• validation and quality control of new/updated application systems
• Perform the testing/UAT for (e)CRF screens, database structure, data loading, etc…


as Clinical Data manager under Clintrial V4 and SAS
July 2006 – January 2004; Oncology area :
• Management of clinical studies from data-base set-up to data-base lock within Clintrial V4.3
• Consistency check and CRF data-quality: clinical data validation, queries management.
• Meetings preparation and organization: data-review, pre-lock meeting, clinical trial team meeting.
• Study documents preparation and update: follow-up with CRF design, preparation of CRF completion guidelines, data entry conventions, data-transfer specification, data-validation plan and data-review plan, Monitoring Plan and Data Management Plan

July 2003 – January 2004; Phase I:
• Management of clinical studies from data-base set-up to data-base lock within Clintrial V4.3
• Consistency check and CRF data-quality: clinical data validation, queries management.
• Meetings preparation and organization: data-review, pre-lock meeting, clinic

-------------------
Modifié par bridg le 22-08-2010 08:44
Titre/anonymat



Réponse: Correction/ resume de fouz94, postée le 25-08-2010 à 09:41:51 (S | E)
MERCI bridg!



[POSTER UNE NOUVELLE REPONSE] [Suivre ce sujet]


<< Thèmes généraux, jeux, chansons


 


> INDISPENSABLES : TESTEZ VOTRE NIVEAU | GUIDE DE TRAVAIL | NOS MEILLEURES FICHES | Les fiches les plus populaires | Une leçon par email par semaine | Exercices | Aide/Contact

> INSEREZ UN PEU D'ANGLAIS DANS VOTRE VIE QUOTIDIENNE ! Rejoignez-nous gratuitement sur les réseaux :
Instagram | Facebook | Twitter | RSS | Linkedin | Email

> NOS AUTRES SITES GRATUITS : Cours de français | Cours de mathématiques | Cours d'espagnol | Cours d'italien | Cours d'allemand | Cours de néerlandais | Tests de culture générale | Cours de japonais | Rapidité au clavier | Cours de latin | Cours de provençal | Moteur de recherche sites éducatifs | Outils utiles | Bac d'anglais | Our sites in English

> INFORMATIONS : Copyright - En savoir plus, Aide, Contactez-nous [Conditions d'utilisation] [Conseils de sécurité] Reproductions et traductions interdites sur tout support (voir conditions) | Contenu des sites déposé chaque semaine chez un huissier de justice | Mentions légales / Vie privée | Cookies. [Modifier vos choix]
| Cours, leçons et exercices d'anglais 100% gratuits, hors abonnement internet auprès d'un fournisseur d'accès. | Livre d'or | Partager sur les réseaux |