10 Pharmacovigilance jobs in the United Arab Emirates
Pharmacovigilance Associate
Posted today
Job Viewed
Job Description
- Location: United Arab Emirates, Dubai
- Target start date: 01/12/2025
iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.
PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.
About The Job
As
Pharmacovigilance Associate
VIE
within our Pharmacovigilance & Safety team, you'll be in charge of assigned operational Pharmacovigilance tasks within the greater gulf countries. You will support the Greater Gulf PV team to ensure that local PV activities are performed in compliance with the GPV policies, as well as global, regional and local PV regulations to warrant safe and appropriate use of Sanofi products on the market in the assigned country(ies), as well as establish and maintain a robust and efficient local PV system by ensuring the availability and implementation of proper systems/procedures, tools and training.
Ready to get started?
Join the engine of Sanofi's mission — where deep immunoscience meets bold, AI-powered research. In R&D, you'll drive breakthroughs that could turn the impossible into possible for millions.
About Sanofi
We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.
Main Responsibilities
- Maintain robust collaboration/interaction with the in-country partner functions, to carry out and monitor local PV activities, in compliance with PV regulatory requirements and company procedures/guidelines.
- Establish and implement processes in compliance with regional/local PV regulations and global Sanofi group procedures and cooperate with the CQH to document them in local Quality Documents as appropriate.
- Manage local compliance metrics generation, Root Cause Analysis (RCA), Corrective Actions/Preventive Actions (CAPAs) implementation and related tracking activities.
- Warrant inspection readiness of the local PV system (auditable trail of all PV activities performed locally is maintained and readily available) with key stakeholders (i.e. Quality, Medical and Regulatory).
- Complete in timely manner audit and inspection observations CAPAs in close interaction with Global/Local Functions.
- Responsible of the oversight of its local PV activities through completion of periodic reports (e.g. PV Activity Report) and providing this oversight to the Region PV Head and GPV SMEs.
- Screen and analyze national regulations, and forward any future/new/updated PV regulation (draft or final) to GPV via Regulatory Intelligence unit and Region PV Head.
Experience
About you
- Experience with pharmacovigilance systems and safety-related product management in both clinical development and marketed products is highly appreciated.
- A minimum of experience in either pharmacovigilance or regulatory or quality or medical or clinical development is necessary.
Soft And Technical Skills
- Interpersonal skills of diplomacy and team player dynamics; knowledge of and respect for cultural differences; professionalism and mediation are important.
- Demonstrate problem solving skills, sense of urgency, capacity to work under pressure.
- Ability to work in international and transversal teams.
- Sufficient knowledge in international and national (Pharmacovigilance) regulations as well as industry standards.
- Sufficient ability to interpret clinical data including safety data.
Education
- Medical Doctor, Pharmacist, Pharm D, Veterinary Doctor, Health Sciences PhD, MPH or Master's degree in a similar field.
Languages
- Proficiency in English (verbal and written) to accurately communicate PV information.
- Arabic knowledge would be a plus.
Why choose us ?
- Be part of a pioneering biopharma company where patient insights shape drug development.
- Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.
- Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.
- Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.
- Help improve the lives of millions of people globally by making drug development quicker and more effective.
iMove is a unique program tailored for European youth interested in challenging themselves with meaningful assignments across the globe. At Sanofi we have a strong ambition to invest in young talents who will drive the success of Sanofi tomorrow.
Sanofi's Work Abroad Program, iMove, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our iMove Work Abroad Program is a unique opportunity to make a difference through your work.
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Pursue
Progress
.
Discover
Extraordinary
.
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what's never-been-done-before. You'll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people's lives? Let's Pursue Progress and Discover Extraordinary – together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
Pharmacovigilance Associate
Posted today
Job Viewed
Job Description
Join to apply for the Pharmacovigilance Associate - VIE Contract role at TALENTMATE
Job Description
- Location: United Arab Emirates, Dubai
- Target start date: 01/12/2025
iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28. Candidates cannot apply to a VIE assignment in their country of citizenship. Applications must be submitted in English and should use a personal email address.
About The Job
As Pharmacovigilance Associate VIE within our Pharmacovigilance & Safety team, you'll be in charge of assigned operational Pharmacovigilance tasks within the greater Gulf countries. You will support the Greater Gulf PV team to ensure that local PV activities are performed in compliance with GPV policies, and with global, regional and local PV regulations to warrant safe and appropriate use of Sanofi products in the assigned country(ies). You will help establish and maintain a robust local PV system by ensuring the availability and implementation of proper systems/procedures, tools and training.
Ready to get started? Join the engine of Sanofi's mission — where deep immunoscience meets bold, AI-powered research.
About Sanofi
We are an R&D-driven, AI-powered biopharma company focused on improving people's lives. Our work spans understanding the immune system and developing medicines and vaccines to treat and protect millions worldwide.
Main Responsibilities
- Maintain robust collaboration with in-country partner functions to carry out and monitor local PV activities, in compliance with PV regulatory requirements and company procedures/guidelines.
- Establish and implement processes in compliance with regional/local PV regulations and global Sanofi procedures; cooperate with CQH to document them in local Quality Documents as appropriate.
- Manage local compliance metrics, Root Cause Analysis (RCA), CAPAs and related tracking activities.
- Warrant inspection readiness of the local PV system with key stakeholders (Quality, Medical, Regulatory).
- Complete audits and inspection observations CAPAs in collaboration with Global/Local Functions.
- Oversee local PV activities through periodic reports and provide oversight to the Region PV Head and GPV SMEs.
- Screen and analyze national regulations and communicate any future/new PV regulations to GPV via Regulatory Intelligence and Region PV Head.
Experience
Experience with pharmacovigilance systems and safety-related product management in clinical development and marketed products is appreciated. A minimum of experience in pharmacovigilance or regulatory or quality or medical or clinical development is necessary.
Soft And Technical Skills
- Diplomacy, teamwork, cultural awareness, professionalism.
- Problem solving, sense of urgency, ability to work under pressure.
- Ability to work in international and transversal teams.
- Knowledge of international and national pharmacovigilance regulations and industry standards.
- Ability to interpret clinical safety data.
Education
- Medical Doctor, Pharmacist, Pharm D, Veterinary Doctor, Health Sciences PhD, MPH or Master's degree in a related field.
Languages
- Proficiency in English (verbal and written) to accurately communicate PV information. Arabic knowledge is a plus.
Why choose us?
- Be part of a pioneering biopharma company where patient insights shape drug development.
- Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.
- Collaborate across diverse, multidisciplinary teams.
- Commitment to diversity, equity, and inclusion with Employee Resource Groups and leadership programs.
- Help improve lives globally by making drug development quicker and more effective.
iMove is a unique program tailored for European youth seeking meaningful assignments across the globe. Sanofi offers jobs with real responsibilities in more than 40 countries. This program invites talented individuals to contribute to solving healthcare needs worldwide.
At Sanofi, we provide equal opportunities to all regardless of race, color, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or protected status by law.
Job Details
- Role Level: Mid-Level
- Work Type: Contract
- Country: United Arab Emirates
- City: Dubai
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#J-18808-Ljbffr
Pharmacovigilance Associate
Posted today
Job Viewed
Job Description
Pharmacovigilance Associate - VIE Contract
iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein, and Iceland) aged between 18 and 28.
PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.
PLEASE NOTE that applications submitted only in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications submitted in English will be considered. Please ensure to apply with your personal email address.
About the job
About Sanofi
Main responsibilities :
- Maintain collaboration with in-country partner functions to carry out and monitor local PV activities, ensuring compliance with PV regulatory requirements and company procedures.
- Establish and implement processes compliant with regional/local PV regulations and global Sanofi procedures, documenting them in local Quality Documents as appropriate.
- Manage local compliance metrics, conduct Root Cause Analysis (RCA), implement Corrective and Preventive Actions (CAPAs), and track related activities.
- Ensure inspection readiness of the local PV system, maintaining an auditable trail of all PV activities and coordinating with stakeholders such as Quality, Medical, and Regulatory teams.
- Complete audit and inspection observations CAPAs in a timely manner, working closely with Global and Local functions.
- Oversee local PV activities through periodic reports (e.g., PV Activity Report) and provide oversight to the Region PV Head and GPV SMEs.
- Review national regulations and communicate updates or new PV regulations to GPV via the Regulatory Intelligence unit and Region PV Head.
About you
Experience :
- Experience with pharmacovigilance systems and safety-related product management in clinical development and marketed products is highly valued.
- A minimum of experience in pharmacovigilance, regulatory affairs, quality, medical, or clinical development is required.
Soft and technical skills :
- Diplomacy, teamwork, cultural awareness, professionalism, and mediation skills are important.
- Problem-solving skills, sense of urgency, and ability to work under pressure.
- Ability to work effectively in international and cross-functional teams.
- Knowledge of international and national pharmacovigilance regulations and industry standards.
- Ability to interpret clinical and safety data.
Education :
- Medical Doctor, Pharmacist, Pharm D, Veterinary Doctor, Health Sciences PhD, MPH, or a Master's degree in a related field.
Languages :
- Proficiency in English (verbal and written) is required.
- Knowledge of Arabic is a plus.
Why choose us?
- Be part of a pioneering biopharma company where patient insights influence drug development.
- Work with AI-powered science that accelerates discovery and improves outcomes.
- Collaborate with diverse, multidisciplinary teams to spark new ideas.
- Join a workplace committed to diversity, equity, and inclusion, with Employee Resource Groups and leadership programs.
- Contribute to improving lives globally by making drug development faster and more effective.
iMove is a unique program for European youth seeking meaningful assignments worldwide. Sanofi is committed to investing in young talents driving our future success.
Sanofi's Work Abroad Program, iMove, offers roles with real responsibilities and growth opportunities across functions such as marketing, finance, regulatory, supply chain, clinical trials, production, and more in over 40 countries. Join us to make a difference in healthcare.
LI-EUR
Pursue, discover
Better medications, outcomes, and science are out there. Progress depends on people from diverse backgrounds, locations, and roles united by a shared goal: making miracles happen. Let's be those people.
Sanofi is an equal opportunity employer, welcoming applicants regardless of race, color, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability, or gender identity.
Learn more about our Diversity, Equity, and Inclusion initiatives at our website.
#J-18808-LjbffrReprésentant en pharmacovigilance
Posted today
Job Viewed
Job Description
Ce poste est disponible dans un contexte de pharmacovigilance et d'information médicale.
Description du posteL'objectif principal est de surveiller la sécurité des produits.
- Surveillance continue du profil de sécurité des produits en développement et commercialisés :
- Valider les livrables des chargés de vigilances
- Surveiller et analyser en continu le profil de sécurité d'emploi et le rapport bénéfice/risque des produits, à partir des informations collectées en France et à l'international
- Relire et argumenter le cas échéant les paragraphes concernant la tolérance des produits dans le protocole d'essais, les brochures investigateurs, les IMPDs, les rapports d'essais cliniques, les dossiers d'AMM
- Vérifier l'existence d'un système de vigilances local
- Rédiger les plans de gestion de risque et en assurer leur diffusion au niveau des filiales
- Rédiger les réponses à toutes les questions émanant des autorités
- Assurer l'activité de détection de signal
- Analyser l'impact des textes réglementaires
- Mettre à jour les procédures inhérentes à l'activité
- Participer aux Due diligence
- Démontage et analyse de textes réglementaires
- Gestion de projet et planification
- Rédaction et communication écrite
- Analyse de données et recherche documentaire
Junior ou débutant
Pour ce poste, nous recherchons un candidat motivé et diplômé avec une bonne connaissance des règles de pharmacovigilance et des lois sanitaires locales. La capacité à travailler en équipe et à communiquer efficacement est essentielle.
Spécialiste de la pharmacovigilance
Posted today
Job Viewed
Job Description
Ce poste vous propose de participer à l'élaboration et à la mise en œuvre d'un système de surveillance continue du profil de sécurité des produits. Vous collaborerez avec les équipes de développement et commercialisation pour valider les livrables des chargés de vigilances.
- Réception et analyse des rapports de signal
- Mise en place et suivi des plans de gestion de risque
- Analyse du rapport bénéfice/risque
Vos compétences en pharmacovigilance, en réglementations pharmaceutiques et en analyse de données seront essentielles pour réussir dans ce rôle.
Pour accomplir ces tâches, vous aurez besoin de bonnes capacités de communication, d'une bonne compréhension des normes internationales et nationales ainsi que des exigences réglementaires.
L'employeur est un leader dans son secteur et offre des opportunités de formation et de développement professionnels importantes.
Pierre Fabre est reconnu comme l'un des meilleurs employeurs au monde. Le groupe est classé dans le Top 10 de l'industrie cosmétique et dans le Top 10 de l'industrie pharmaceutique mondiale.
Pharmacovigilance and medical information associate
Posted today
Job Viewed
Job Description
Pharmacovigilance and medical information associate page is loaded Pharmacovigilance and medical information associate Apply locations UAE - Dubai time type Full time posted on Posted 5 Days Ago job requisition id JR Who we are ?
Pierre Fabre is the 2nd largest dermo-cosmetics laboratory in the world, the 2nd largest private French pharmaceutical group and the market leader in France for products sold over the counter in pharmacies.
Its portfolio includes several medical franchises and international brands including Pierre Fabre Oncologie, Pierre Fabre Dermatologie, Eau Thermale Avène, Klorane, Ducray, René Furterer, A-Derma, Naturactive, Pierre Fabre Oral Care.
Established in the Occitanie region since its creation, and manufacturing over 95% of its products in France, the Group employs some 10,000 people worldwide. Its products are distributed in about 130 countries.86% of the Pierre Fabre Group is held by the Pierre Fabre Foundation, a government-recognized public-interest foundation, while a smaller share is owned by its employees via an employee stock ownership plan.
In 2019, Ecocert Environment assessed the Group’s corporate social and environmental responsibility approach in accordance with the ISO 26000 sustainable development standard and awarded it the “Excellence” level.
Pierre Fabre is recognized as one of the "World's Best Employers 2021" by Forbes. Our group is ranked in the Top 3 in the cosmetics industry and in the Top 10 in the pharmaceutical industry worldwide.
Assurer la surveillance continue du profil de sécurité des produits en développement et commercialisés :
-Valider les livrables des chargés de vigilances
-Surveiller et analyser en continu le profil de sécurité d’emploi et le rapport bénéfice/risque des produits, à partir des informations collectées en France et à l’international
-Relire et argumenter le cas échéant les paragraphes concernant la tolérance des produits dans le protocole d’essais, les brochures investigateurs, les IMPDs, les rapports d’essais cliniques, les dossiers d’AMM
-Vérifier l'existence d'un système de vigilances local
-Rédiger les plans de gestion de risque et en assurer leur diffusion au niveau des filiales
-Rédiger les réponses à toutes les questions émanant des autorités
-Assurer l'activité de détection de signal
-Analyser l'impact des textes réglementaires
-Mettre à jour les procédures inhérentes à l'activité
-Participer aux Due diligence
We are convinced that diversity is a source of fulfillment, social balance and complementarity for our employees, which is why our offers are open to all, without restriction.
#J-18808-LjbffrPharmacovigilance and medical information associate
Posted today
Job Viewed
Job Description
Qui sommes-nous ?
Pierre Fabre est le 2ème laboratoire dermo-cosmétique mondial, le 2ème groupe pharmaceutique privé français et le leader des produits vendus hors prescription dans les pharmacies en France.
Son portefeuille compte plusieurs franchises médicales et marques internationales dont Pierre Fabre Oncologie, Pierre Fabre Dermatologie, Eau Thermale Avène, Klorane, Ducray, René Furterer, A-Derma, Naturactive et Pierre Fabre Oral Care.
Implanté depuis toujours en région Occitanie, fabricant plus de 95% de ses produits en France, le groupe emploie près de collaborateurs dans le monde et distribue ses produits dans quelque 130 pays. Pierre Fabre est détenu à 86% par la Fondation Pierre Fabre, une fondation reconnue d'utilité publique, et secondairement par ses collaborateurs à travers un plan d'actionnariat salarié.
En 2021, Ecocert Environnement a évalué la démarche de responsabilité sociétale et environnementale du Groupe selon la norme ISO 26000 du développement durable et lui a attribué le niveau « Excellence ».
Pierre Fabre est reconnu comme l'un des « Meilleurs Employeurs du Monde 2021 » par Forbes. Notre groupe est classé dans le Top 6 de l'industrie cosmétique et dans le Top 7 de l'industrie pharmaceutique dans le monde. Nous sommes convaincus que notre engagement et notre passion font préserver notre indépendance et vivre notre raison d'être.
Votre mission
Assurer la surveillance continue du profil de sécurité des produits en développement et commercialisés :
- Valider les livrables des chargés de vigilances
- Surveiller et analyser en continu le profil de sécurité d'emploi et le rapport bénéfice/risque des produits, à partir des informations collectées en France et à l'international
- Relire et argumenter le cas échéant les paragraphes concernant la tolérance des produits dans le protocole d'essais, les brochures investigateurs, les IMPDs, les rapports d'essais cliniques, les dossiers d'AMM
- Vérifier l'existence d'un système de vigilances local
- Rédiger les plans de gestion de risque et en assurer leur diffusion au niveau des filiales
- Rédiger les réponses à toutes les questions émanant des autorités
- Assurer l'activité de détection de signal
- Analyser l'impact des textes réglementaires
- Mettre à jour les procédures inhérentes à l'activité
- Participer aux Due diligence
Qui êtes-vous ?
Nous sommes convaincus que la diversité est une source d'épanouissement, d'équilibre social et de complémentarité pour nos collaborateurs, nos offres sont donc ouvertes à toutes et tous sans restriction.
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About the latest Pharmacovigilance Jobs in United Arab Emirates !
Pharmacovigilance and medical information associate
Posted today
Job Viewed
Job Description
Pierre Fabre is the 2nd largest dermo-cosmetics laboratory in the world, the 2nd largest private French pharmaceutical group and the market leader in France for products sold over the counter in pharmacies.
Its portfolio includes several medical franchises and international brands including Pierre Fabre Oncologie, Pierre Fabre Dermatologie, Eau Thermale Avène, Klorane, Ducray, Ren, Furterer, A-Derma, Naturactive and Pierre Fabre Oral Care.
Established in the Occitanie region since its creation and manufacturing over 95% of its products in France, the Group employs some 10,000 people worldwide. Its products are distributed in about 130 countries. 86% of the Pierre Fabre Group is held by the Pierre Fabre Foundation, a government-recognized public-interest foundation, while a smaller share is owned by its employees via an employee stock ownership plan.
In 2019 Ecocert Environment assessed the Group's corporate social and environmental responsibility approach in accordance with the ISO 26000 sustainable development standard and awarded it the Excellence level.
Pierre Fabre is recognized as one of the World's Best Employers 2021 by Forbes. Our group is ranked in the Top 3 in the cosmetics industry and in the Top 10 in the pharmaceutical industry worldwide.
Your missionAssurer la surveillance continue du profil de sécurité des produits en développement et commercialisés :
- Valider les livrables des chargés de vigilances
- Surveiller et analyser en continu le profil de sécurité d emploi et le rapport bénéfice/risque des produits à partir des informations collectées en France et à l international
- Relire et argumenter le cas chant les paragraphes concernant la tolérance des produits dans le protocole des essais, les brochures investigateurs, les IMPDs, les rapports d essais cliniques et les dossiers d AMM
- Vérifier l existence d un système de vigilances local
- Rédiger les plans de gestion de risque et en assurer leur diffusion au niveau des filiales
- Rédiger les réponses à toutes les questions émanant des autorités
- Assurer l activité de détection de signal
- Analyser l impact des textes réglementaires
- Mettre à jour les procédures inhérentes à l activité
- Participer aux Due Diligence
We are convinced that diversity is a source of fulfillment social balance and complementarity for our employees which is why our offers are open to all without restriction.
Required Experience:
IC
#J-18808-LjbffrPharmacovigilance and medical information associate
Posted today
Job Viewed
Job Description
Pharmacovigilance and medical information associate page is loaded
Pharmacovigilance and medical information associate Apply locations UAE - Dubai time type Full time posted on Posted 5 Days Ago job requisition id JR Who we are ?Pierre Fabre is the 2nd largest dermo-cosmetics laboratory in the world, the 2nd largest private French pharmaceutical group and the market leader in France for products sold over the counter in pharmacies.
Its portfolio includes several medical franchises and international brands including Pierre Fabre Oncologie, Pierre Fabre Dermatologie, Eau Thermale Avène, Klorane, Ducray, René Furterer, A-Derma, Naturactive, Pierre Fabre Oral Care.
Established in the Occitanie region since its creation, and manufacturing over 95% of its products in France, the Group employs some 10,000 people worldwide. Its products are distributed in about 130 countries.86% of the Pierre Fabre Group is held by the Pierre Fabre Foundation, a government-recognized public-interest foundation, while a smaller share is owned by its employees via an employee stock ownership plan.
In 2019, Ecocert Environment assessed the Group's corporate social and environmental responsibility approach in accordance with the ISO 26000 sustainable development standard and awarded it the "Excellence" level.
Pierre Fabre is recognized as one of the "World's Best Employers 2021" by Forbes. Our group is ranked in the Top 3 in the cosmetics industry and in the Top 10 in the pharmaceutical industry worldwide.
Your missionAssurer la surveillance continue du profil de sécurité des produits en développement et commercialisés :
-Valider les livrables des chargés de vigilances
-Surveiller et analyser en continu le profil de sécurité d'emploi et le rapport bénéfice/risque des produits, à partir des informations collectées en France et à l'international
-Relire et argumenter le cas échéant les paragraphes concernant la tolérance des produits dans le protocole d'essais, les brochures investigateurs, les IMPDs, les rapports d'essais cliniques, les dossiers d'AMM
-Vérifier l'existence d'un système de vigilances local
-Rédiger les plans de gestion de risque et en assurer leur diffusion au niveau des filiales
-Rédiger les réponses à toutes les questions émanant des autorités
-Assurer l'activité de détection de signal
-Analyser l'impact des textes réglementaires
-Mettre à jour les procédures inhérentes à l'activité
-Participer aux Due diligence
We are convinced that diversity is a source of fulfillment, social balance and complementarity for our employees, which is why our offers are open to all, without restriction.
#J-18808-LjbffrAssistant pharmacovigilance et informations médicales
Posted today
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Job Description
Mission de pharmacovigilance et d'informations médicales
L'assistant de pharmacovigilance et d'informations médicales est chargé de la surveillance continue du profil de sécurité des produits en développement et commercialisés.
Compétences requises- Avoir une bonne compréhension des règles réglementaires
- Pouvoir analyser des données complexes
- Avoir une excellente capacité d'écriture et de communication
- Diplôme dans un domaine lié à la santé ou à la pharmacie
- Expérience dans un rôle similaire
- Anglais (compétence courante)
Nous recherchons un candidat motivé par la recherche et la prise de décision. Vous serez impliqué dans la validation des livrables des chargés de vigilances et l'analyse du profil de sécurité des produits.