20 offres d'emploi Director Medical Affairs - France |
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Lieu : France
Société : elemed
Take the lead in directing and monitoring all medical activities,..Maintain coherence between our Core Markets and France medical strategies and global directives,..
Postuler | Plus d'offres Director Medical Affairs
Plus d'offres - France |
Lieu : France
Société : Meet
regulatory affairs and others) Liaison with Healthcare Professionals,..PhD or PharmD in a relevant field 4 years' experience in medical affairs within the pharmaceutical / biotech industry Strong scientific and clinical knowledge in oncology (or similar) Excellent comm..
Postuler | Plus d'offres Medical Affairs Manager
Plus d'offres - France |
Lieu : Auvergne-Rhône-Alpes
Société : Mantell Associates
Mantell Associates is partnered with a growing Medical Devices organisation in their search for a Regulatory Affairs Manager...
Postuler |
Lieu : Auvergne-Rhône-Alpes
Société : Mantell Associates
searching for a Regulatory Affairs Manager to participate in the registration/renewal and modifications of export products...
Postuler |
Lieu : France
Société : Skills Alliance
as well as working with Medical Affairs on development plans,..Ability to identify discrepancies in clinical trial data and to write queries from a medical perspective...
Postuler | Plus d'offres Medical Director - Clinical Development
Plus d'offres - France |
Lieu : France
Société : CDG CONSEIL
la créativité,..L'agilité,..médecin) est requise avec une expérience d'au moins 3 ans sur un poste médical dans l'industrie pharmaceutique...
Postuler |
Lieu : France
Société : CDG CONSEIL
Il est indispensable de maîtriser la méthodologie des essais cliniques et des études observationnelles...l'autonomie et l'organisation sont des qualités recherchées...
Postuler |
Lieu :
Société : Chronos Consulting
They are looking for a Clinical Affairs Program Manager Europe...you will be responsible for developing strategies for a successful execution of roadmap clinical trials that demonstrate medical product safety and efficacy...
Postuler |
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Lieu : Ile-de-France
Société : SUN PHARMA
..utilizing scientific and medical evidence-based information Strategically prepare and support the development,..
Postuler | Plus d'offres Medical Manager
Plus d'offres - Ile-de-France |
Lieu : Sarlat-la-Canéda
Société : Barrington James
Regulatory Affairs,..We are dedicated to advancing innovative treatments to address unmet medical needs and improve patient lives...
Postuler | Plus d'offres Director of Process Development
Plus d'offres - Sarlat-la-Canéda |
Lieu : France
Société : The Medical Affairs Company
and consistent medical and scientific support and communications...Collaborate with Medical Affairs,..
Postuler |
Lieu : Paris
Société : CARVALONN EXECUTIVE SEARCH
regulataory,..Medical affairs,..budgets and quality standard of pharmaceutical industrie Hor she will work closely with CMC,..
Postuler |
Lieu : Hauts-de-Seine
Société : CABINET CARVALONN
for an added value in commercializing the products according to timelines,..EXPERIENCE IN FOOD COMPLEMENT IS REQUIRED AND MANDATORY FOR THIS ROLE ..
Postuler | Plus d'offres PROJECT MANAGER FOOD COMPLEMENTARY
Plus d'offres - Hauts-de-Seine |
Lieu : milan
BOSTON SCIENTIFIC
Boston Scientific Boston Scientific is transforming lives through innovative medical solutions...
Postuler |
Lieu : Nord
Société : Arthur Hunt Group
Your main tasks will be to lead and manage certification projects on the US market,..FDA) the project management methodology project teams in interaction with international teams planning that budgets are respected risks and monitor action plans US marketing authorisations...
Postuler |
Lieu : France
Société : Barrington James
5 years within Regulatory Affairs Dermatology or Gene therapy is a bonus Experience in early phase trials Scientific academic background HOW TO APPLY By clicking "apply" you will be sending your CV to Courtney Laidler at Barrington James...
Postuler |
Lieu : Paris
Société : neuroClues
and Good Clinical Practice (preferably ISO 14155) applied to innovative medical technologies...Work closely with regulatory affairs and product management teams to prepare and submit documentation for regulatory approvals of clinical investigations...
Postuler | Plus d'offres Head of Clinical
Plus d'offres - Paris |
Lieu : Dreux
Société : Proclinical Staffing
change controls) in line with defined KPIs...Evaluate impact of changes to the project scope,..Good communication skills and ability to work in a matrix and global environment...
Postuler |
Lieu : Paris
Société : Institut du Cerveau Paris Brain Institute
Communicate and champion the institute's open science strategy and accomplishments in collaboration with the scientific and medical affairs department,..
Postuler |
Lieu : créteil
You will be in charge to support our main medical suppliers in order to monitor,..facilitator and very structured
Capacity to analyze and integrate products features and impacts of tests or quality results
Knowledge of Medical Devices Regulation appreciated
CAN..
Postuler | Plus d'offres Product Quality Engineer
Plus d'offres - créteil |
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