Hybrid Jobs in Hauts-de-France, France

Direction Médicale, Patient, Consommateur (DMPC) Innovation DATA team drives data product strategy for healthcare consumers. The Data Product Owner leads end‑to‑end data projects, defines requirements, manages budgets, coordinates stakeholders, and oversees change management and deployment.

Pôle d'Expertise Paie at Spie batignolles handles payroll and personnel administration for the Civil Engineering & Foundations division. The Payroll Manager processes payroll, validates time‑cards, prepares monthly DSNs, manages contract terminations and oversees hiring formalities and benefits administration.

Pôle d'Expertise Paie at Spie batignolles manages payroll and personnel administration for the Génie civil & fondations division. The role processes payroll, validates time‑keeping data, prepares monthly DSN filings and handles contract terminations and employee onboarding.

Pierre Fabre seeks a Global Medical Advisor in Oncology for a 6‑month fixed‑term contract to support the Medical Lead in developing and implementing medical strategy for metastatic colorectal cancer. Responsibilities include coordinating medical plans, ensuring scientific omnichannel communication, developing content, engaging key external contacts, and reviewing internal materials.

Pierre Fabre, a leading dermo‑cosmetics and pharmaceutical group, seeks a Translational PK/PD Modeler to join its PKPD/Tox Modeling & Simulation Team in Toulouse. The role involves developing advanced oncology PK/PD models, guiding dose selection, supporting IND submissions, and communicating results to cross‑functional stakeholders.

Pierre Fabre, a leading dermo‑cosmetics and pharmaceutical group, seeks a Global Customer Innovation Manager to drive omnichannel engagement across franchises and markets. The role leads design and rollout of initiatives enhancing Healthcare Professional (HCP) understanding and engagement, bridging franchise, medical, and affiliate teams.

Pierre Fabre seeks a Global Customer Excellence Lead to drive transformation of sales force effectiveness for healthcare professionals. Lead CRM rollout, change management, omnichannel HCP journey mapping, segmentation, incentive design, and territory alignment.

Pierre Fabre, a leading dermo‑cosmetics and pharmaceutical group, seeks a Safety Officer (Vigilance Associate – Periodic Reports) for a 6‑month contract to replace maternity leave. Based in Hauts‑de‑Seine, France, the role involves drafting and quality‑controlling PSURs, PBRERs, DSURs and other periodic vigilance reports, ensuring timely submission to subsidiaries, partners and regulatory authorities, and maintaining traceability and archiving.

Pierre Fabre, a leading dermo‑cosmetics and pharmaceutical group, seeks a Global Market Access Senior Manager to develop pricing and reimbursement strategies for oncology and rare disease products. The role involves collaborating with the Global Market Access Director, validating country dossiers, anticipating payer objections, supervising consultants, maintaining pricing conditions for mature products, conducting price impact and IRP analyses, and participating in pricing committees.

Pierre Fabre is the 2nd largest dermo‑cosmetics laboratory in the world and a leading French pharmaceutical group. The company employs about 10,000 people worldwide and distributes products in 130 countries.

Pierre Fabre seeks a Project Manager for Real‑World Evidence studies in dermatology and pharma. The role involves leading cross‑functional teams, coordinating CROs, ensuring regulatory compliance, managing budgets, and delivering high‑quality data.

Pierre Fabre, a leading French dermo‑cosmetics and pharmaceutical group, seeks a Regulatory CMC Development Expert to strengthen its Worldwide Regulatory Affairs team. The role focuses on crafting and executing CMC regulatory strategies from early clinical stages to marketing authorization, collaborating closely with pharmaceutical development and regulatory teams.

Pierre Fabre seeks a senior Clinical Development Safety Statistics Expert to lead safety signal detection, benefit–risk evaluation, and regulatory compliance across oncology trials. The role involves designing safety processes, coordinating reviews, developing analytics tools, and collaborating with R&D stakeholders, with up to two remote days per week.

Pierre Fabre, a leading French dermo‑cosmetics and pharmaceutical group, seeks a Lead Statistical Programmer to strengthen its Biometry Department. The role focuses on designing, executing, and validating statistical programs for randomized controlled trials (RCTs) and real‑world evidence (RWE) studies, ensuring compliance with regulatory standards such as ICH, EMA, FDA, and PMDA.

Ajax Systems seeks an Area Sales Manager for Île‑de‑France to drive regional sales, build client relationships, and collaborate with cross‑functional teams. The role involves regular client visits, market analysis, and achieving commercial targets in a fast‑growing security technology company.

Pierre Fabre, a leading dermo‑cosmetics and pharmaceutical group, seeks a Chef de Projets – Etudes RWE to manage medical data generation projects within its PMO. Based in Boulogne or Toulouse, the role combines project leadership, budget oversight, and coordination of CRO partners to ensure data quality, cost control, and regulatory compliance. Responsibilities include setting up project plans, monitoring performance, supervising CROs, developing risk and communication plans, and collaborating with medical writers on study protocols.

Pierre Fabre, a leading dermo‑cosmetics and pharmaceutical group, seeks a Lead Statistician – Real World Evidence to join its Biometry Department in Toulouse or Boulogne, with the option to work remotely or in a hybrid model. The role requires deep expertise in RWE study design, sample size calculation, protocol writing, and statistical analysis plan development, as well as proficiency in SAS and knowledge of regulatory guidelines (ICH, EMA, FDA, NICE, ENcEPP).

AI & Data Transformation Office (ADTO) at Aneo, a boutique tech consultancy helping CAC 40 and scale‑up clients move AI projects from experimentation to production at scale in regulated finance environments. The Senior MLOps & AI Lead defines AI/GenAI strategy, designs and operates scalable AI infrastructure on‑prem, cloud or hybrid, and guides clients through architecture, cost, compliance and industrialisation.

Regulatory Affairs team in AbbVie France Oncology/Hematology division ensures compliance and market access for oncology and hematology products. The role manages promotional material review, drug registration dossiers, and regulatory submissions while collaborating with marketing, medical, and European regulatory contacts.

Regulatory Affairs team at AbbVie France ensures compliance and market access for oncology/hematology products. The role manages promotional material review, drug registration dossiers, and supports market access strategy while coordinating with European regulatory contacts.