Pharmacoepidemiologist M / F

AIXIAL GROUP; Paris; Sur place; EUR 40 000 - 80 000; Plein temps

Résumé du poste

Une entreprise innovante recherche un Pharmacoépidémiologiste passionné pour rejoindre une équipe dynamique et internationale. Dans ce rôle, vous contribuerez à des avancées significatives dans la recherche clinique, en assurant la qualité scientifique des études et en collaborant avec des équipes multidisciplinaires. Vous aurez l'opportunité de travailler sur des projets qui impactent positivement la vie de millions de personnes à travers le monde. Avec un engagement envers le développement de carrière et la diversité, cette entreprise offre un environnement propice à la croissance personnelle et professionnelle. Rejoignez-nous pour faire la différence dans le domaine des sciences de la vie.

Prestations

Développement de carrière

Environnement de travail inclusif

Mentorat et coaching

Impact positif sur la santé globale

Qualifications

• 5+ années d'expérience dans un poste similaire.
• Diplôme en santé publique, épidémiologie ou domaine équivalent.

Responsabilités

• Assurer la qualité scientifique des études confiées.
• Gérer l'évaluation épidémiologique des signaux de sécurité.
• Rédiger des résumés pour les autorités réglementaires.

Connaissances

Gestion de projet

Compétences en écoute

Diplomatie

Analyse de la littérature scientifique

Rédaction de documents réglementaires

Travail en équipe multidisciplinaire

Formation

Master (BAC+5)

PhD

PharmD

Description du poste

You are a highly skilled professional with passion for the world of life sciences and clinical research? You want to thrive in a dynamic and collaborative international environment where your expertise directly impacts people's lives? Come and join Aixial Group to contribute to shaping the future of clinical research!

We are currently looking for a Pharmacoepidemiologist M / F to carry out the following tasks (non-exhaustive list) :

• Ensuring the scientific quality of entrusted studies (protocols, statistical analysis plans, study reports, result interpretation, study documents, project meetings)
• Ensuring the operational follow-up of entrusted studies (management of service providers, management of internal procedures related to studies)
• Managing the epidemiological evaluation of safety signals (review and analysis of scientific literature)
• Contributing to updates of crisis management plans, responses to health authority queries, and participation in cross-functional meetings (with pharmacovigilance, medical affairs, and regulatory affairs)
• Writing summaries in a confidential context towards regulatory authorities
• Carefully following operational procedures while respecting deadlines
• Analyzing pharmacoepidemiological scientific literature for safety signals / SER, RMP, PBRER / PSUR
• Reviewing protocols, statistical analysis plans, and study reports for PASS (Post-Authorisation Safety Study)
• Ensuring compliance with submission timelines of PASS study documents to regulatory authorities

Your profile :

• You have a Master's degree (BAC+5), PhD, PharmD with a specialization in public health, epidemiology, or equivalent field of study
• You have at least 5 years of experience in a similar position
• Ability to manage a project and work transversally in multidisciplinary teams: medical, regulatory, marketing, etc.
• You have good listening skills and diplomacy
• You are fluent in English (written and spoken)
• You have a professional or fluent level in French would be a plus

Who Are we?

• We are one of the world’s leaders in CRO (Contract Research Organisation) with the commitment, expertise, and flexibility needed to deliver efficient clinical trials.
• We work with global pharmaceutical, biotech, cosmetic, medical device, and many other companies around the globe, providing them with innovative and scalable solutions.
• We are operating in 10 countries across 3 continents, bringing together over 1000 talented professionals dedicated to making a positive impact in the life sciences industry.
• We have been part of ALTEN Group since 2014 and are continuously exploring new opportunities to expand our activity worldwide.

Why Join Us?

• Make a positive impact and be at the forefront of the project: You will be part of groundbreaking advancements in clinical research that have positive impacts on millions of people’s lives globally.
• Career Development: People are our biggest asset. We are committed to empowering our team continually and building a positive and supportive environment that fosters growth, flexibility, and teamwork. At Aixial Group, you will be coached and mentored throughout your journey to help you advance your professional and personal growth.
• Our commitment to Diversity, Equality, and Inclusion: We aim to create a workforce that promotes dignity and respect, where individual differences are recognized and valued, and where each employee can give their best. Gender equality is at the core of the development strategy of Aixial Group.

Aixial Group continues to grow and recruit in the clinical trial professions.

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