Vincent Demeautis Email & Phone Number

Région De Lausanne, Suisse

People Management : - Responsible and accountable for managing and supporting a team of Clinical Trial Managers as direct report (up to 5 CTMs). - Allocate resources, coach and tracks performance of CTMs with the objective to ensure an optimal planification, performance and leadership on the clinical trials.Clinical Operations Program Lead :- For 1 major compound (Program Strategy, Roadmap Development, Presentation to Management, Point of Escalation..)Study Management (Clinical Trial Manager Role) :- For 1 Phase I Study - Outsourced (Oncology) - Lead the clinical study, Responsible for the overall operational management and delivery of clinical studies on time, within budget and quality, in accordance with the global objectives of the project.Initiation and development of an innovative and standardized Study Dashboard :- Based on PowerBI technology with a cross-functional team - Fulfills unmet needs / high added-value / limited investment- Project awarded in 2021 (Debiopharm Shapers Award)

Lausanne, Vaud, Suisse

People Management : - Manage the Clinical Trial Associates (CTAs) team (Team expansion from 4 FTEs to 10 FTEs)- Allocate resources and tracks performance with the objective to ensure an optimal, efficient, standardized and proactive support to the CTMs and the Clinops Director. - Developed CTAs skills and expertise (Subject Matter Experts : Budget, Insurance, Minutes, Ct.gov, Trackers..).Study Management (Clinical Trial Manager Role) since 2018 :- Lead the clinical study, Responsible for the overall operational management and delivery of clinical studies on time, within budget and quality (ICH GCP, applicable local laws, SOP/OIs), in accordance with the global objectives of the project.• 2 Phase I Studies - Managed in-house (Oncology)• 1 Phase II Study – Outsourced – Re-setup following study hold (Infectious Disease)- Clinical Operations Program Lead for 1 major compoundCTM support until end of 2017 :- Provided an optimal, standardized and proactive support (Timelines, Budget, Process, Feasibility, Setup, Vendor Management, KPIs, Tools…) to the Clinical Trial Managers on 5 studies (Phase I and II – Outsourced - Oncology and Infectious disease)Transversal Activities – Project Management – Innovation:- Initiation of the implementation of a new eTMF platform (Veeva Vault) including Market screening, Business Case approval by management, System validation, Processes, Reports/Dashboards…- Coordinate creation, optimization and update of efficient reporting tools (e.g. Clinical Trial Management System (CTMS), Follow-up charts, Study Databases, Dashboards…).- SME for ClinOps Planning Management - Administrator of ClinOps Project Web Access - Supervision and coordination of ClinicalTrials.gov maintenance activities for Debiopharm

Lausanne Area, Switzerland

CTM Support : - Provided an optimal, standardized and proactive support (Timelines, Budget, Process, Feasibility, Setup, Vendor Management, KPIs, Tools…) to the Clinical Trial Managers on 5 studies (Phase I and II Oncology and Infectious disease and 1 Phase III pediatric), in accordance with the global objectives of the projects and SOPs/OIs, with the objective to develop and monitor clinical studies efficiency.Planning Management and Microsoft Project Subject Matter Expert- Providing daily support and trainings to the clinical operations teams.In-house CTMS Subject Matter Expert (Clinsight - CS Monitor): - Design, Setup and support to the teams

Lausanne Area, Switzerland

- Remote-Monitoring of clinical studies (Early Phase - Oncology)- Implementation of Planning Management Process and Tools (MS Project Server) at Clinical Trial Level.- Proactive support to the Clinical Trial Manager for clinical study activities with respect to time and quality (ICH GCP, applicable local laws), in accordance with the objectives of the project and SOPs/OIs.

France

-Developed an Internet platform of private sales specialized in service providers.-Unique and original concept allowing professionals to independently manage their customers development by offering short-term “Deals” -The company has been closed in 2012

Gaillard - France

-Daily Screening, Evaluation and Negotiation of new business opportunities -Daily Country Project Portfolio Management (10 NPD / 2 Licensing-In) with coordination of a team of 8 specialists.-Implementation of a new Idea Generation Process in 3 months-Project officer for the Gaillard Industrial site carve-out project for 6 months

Gaillard - France

-Daily Project Management for 5 brands + Market Intelligence activities-Reintegration of a Bayer subsidiary (Strategic directions, Process, Project pipeline, P&L considerations...) in 6 months and +20% EBIT as a result.-Implementation of a new reporting tool which improved the daily sales overview and accuracy of business platform in 3 months-Local Project management Optimization (Process, method and tools) in collaboration with Global HQ in 6 months and +15% time saving as a result.

-Daily Project management on 3 local brands.-Participation in marketing plans and commercial actions of new products for 2 strong brands on the OTC market: Supradyn and Rennie

Certificate, Project Management, Project Management, With Honours

Partnership between “Université de Savoie” and HEC Geneva (Double degree) Project Management and Health Institution Management.

Master, Law, Economics And Management, Specializing In Health Project Management, Project Management, With Honours

Clinical Research Associate Professional Training, Clinical Research

• Job Preparation : Missions, Responsibilities, Attitudes, Knowledge • Regulatory Trainings : ICH-GCP, Pharmacovigilance, Local.

Bachelor, Biology

Activities and Societies: – With honours – GRENOBLE - Specialities : Animal biology, Neurosciences and Immunology