Stanislas Buffet Email & Phone Number

Boudry

11 months contract

- Importation et distribution of champagne produced by independent winegrowers- Management of champagne tasting events for corporate or private clients- Refletdesbulles.ch online web site management- Champagne wine presentation during trade exhibition (Champagne trade exhibition (Geneva, Zürich), wedding salon (Genève, Lausanne), Arvinis at Montreux))

Vernier - Geneva

- Adverse Event case processing: receipt, data entry, coding, and evaluation of Adverse Event reports according to the applicable SOPs, including writing the narrative; perform seriousness, listedness and causality assessment- Performing global and local literature review- Acting as SME (Subject Matter Expert) and providing training about littérature review processes- Writing of procedural documents such as Adverse Event Reporting Plans (AERPs)

Genève

- Write safety sections of trial related documents (e-g- protocol, informed consent, case report form, SAE form, monitoring plan, Interactive Voice Response System specifications, SAE reconciliation plan) and coordinate review of these sections by Medical Evaluation if necessary- Prepare Periodic SUSAR reports as per Working Instructions- Write the Drug Safety Manual in collaboration with GDS Safety Data management and GDS Regions management- Review documents related to outsourcing… Show more - Write safety sections of trial related documents (e-g- protocol, informed consent, case report form, SAE form, monitoring plan, Interactive Voice Response System specifications, SAE reconciliation plan) and coordinate review of these sections by Medical Evaluation if necessary- Prepare Periodic SUSAR reports as per Working Instructions- Write the Drug Safety Manual in collaboration with GDS Safety Data management and GDS Regions management- Review documents related to outsourcing (e.g. CRO contracts, Request for Proposals and Service Agreements with CROs) and approve decision of outsourcing GDS activities related to trials Show less

- Review and comment on protocol, statistical analysis plan, data entry guideline and study report- Create, review and finalize CRF/eCRF based on standardized CRF pages and input from team- Management of the trial to completion : represent DM on trial Implementation Team and provide the DM team with the information and guidance to complete the project. Create and maintain DM study documentation. Ensure adequate filing and archiving of relevant data and documentation- Code data… Show more - Review and comment on protocol, statistical analysis plan, data entry guideline and study report- Create, review and finalize CRF/eCRF based on standardized CRF pages and input from team- Management of the trial to completion : represent DM on trial Implementation Team and provide the DM team with the information and guidance to complete the project. Create and maintain DM study documentation. Ensure adequate filing and archiving of relevant data and documentation- Code data Concomitant Medications with coding dictionary (WHODrug)- Assist database developer in development of clinical databases and programming of validation checks as applicable. Prepare annotated CRFs/eCRFs as specified Show less

Clinical Database cleaning

Master Degree In R&D Project Management, Optional Subject – Data Management

Project management, quality management, team management and communication, operational planning, marketing. Database creation, management.

Wine Sommelier Certificate, Wine & Spirits

Master’S Degree Equivalency, Physiology And Cellular Biology - Optional Subject – Microbiology

Bachelor'S Degree, Physiology And Cellular Biology - Optional Subject – Microbiology

University General Studies Degree (Deug), Life And Earth Science