Non-clinical Drug Safety Study Monitor

Summary / purpose of the position Schedule, Design, Supervise, and Review toxicology and safety pharmacology invitro and invivo studies Ensure that toxicology dossiers of Ipsen products are designed and conducted in compliance with international regulatory requirements and internal Ipsen procedures for clinical evaluation and regulatory registration Create...

Job Description: Participate in the development of documents covering Safety aspects in clinical studies/investigations such as: investigator brochure, protocol, safety plan, statistical analysis plan, etc. Analyze the effects and adverse events of pharmaceutical products and medical devices, identify potential cases of PV/MV and ensure their reporting in...

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 800 Excelyates. Our unique one-stop provider service model - leveraging full-service,...

**KELLY OCG**, est une société de prestation de services intellectuels dédiée aux industries de santé. Notre savoir-faire, le domaine des **Life Sciences**. Notre client est un laboratoire pharmaceutique international, qui s’engage pour le progrès thérapeutique au bénéfice des patients, en lien avec les professionnels de santé. Sa croissance...

We are looking for a Medical Director in the Rare Diseases Therapeutic Area to join our Clinical Development team. The Medical Development Director will provide medical guidance and leadership in the design, implementation, monitoring and interpretation of our clinical development programs in rare liver diseases. **Main responsibilities / job...

We are looking for a Medical Director in the Rare Diseases Therapeutic Area to join our Clinical Development team. The Medical Development Director will provide medical guidance and leadership in the design, implementation, monitoring and interpretation of our clinical development programs in rare liver diseases.Main responsibilities / job expectationsMain...

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 800 Excelyates. Our unique one-stop provider service model - leveraging full-service,...

**Title**: Clinical Trial Associate (CTA) H/F **Company**: Ipsen Pharma (SAS) To assist in the delivery of Clinical Development objectives and achieve Clinical Operation Excellence, mainly by supporting the Clinical Research Manager (CRM)/Clinical Project Manager (CPM) in administrative activities within the conduct of the clinical studies. To also...

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care.We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model – leveraging full-service,...

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model – leveraging full-service,...

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care.We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 900 Excelyates. Our unique one-stop provider service model – leveraging full-service,...

**Purpose of the position** The Clinical Partnerships Oversight Manager is responsible for supporting the management of Ipsen’s relationships with it’s Service Providers (CROs) within Clinical Development. They are a critical player in the Service Provider Governance and Escalation structure, working to support the Clinical Partnerships Oversight...

**Title**: SVP, Head of Global Patient Safety **Company**: Ipsen Pharma (SAS) - The Senior Vice President, Global Patient Safety is accountable to define the overall Patient Safety strategy for Ipsen across the portfolio (Oncology, Neurosciences, Rare Diseases) from Discovery to development and post marketing approvals’ maintenance, in order to meet...

Ipsen is a dynamic and growing global specialty-driven biopharmaceutical company focused on innovation and specialty care. We aim to make a sustainable difference by significantly improving patients’ health and quality of life and providing them with effective therapeutic solutions for unmet medical needs through differentiated and innovative medicines in...

**Main responsibilities / job expectations** **Main Medical Writing responsibilities** - Manages the preparation of regulatory documents e.g. CSRs, briefing documents, meeting requests, Clinical modules. - Leads Writing/Editing complex Clinical Dossiers/Safety Reports - Reviews documents to ensure compliance with documentation quality standards and...

**Title**: IT Business Analyst Clinical **Company**: Ipsen Pharma (SAS) The role of IT Clinical Development Domain (CDO) and will be empowered to - Leads the analysis of business problems and the translation of business requirements into successful technical solutions and processes to meet business needs. - Analyze business partner’s operations to...

**Title**: IT Business Analyst Clinical **Company**: Ipsen Pharma (SAS) The role of IT Clinical Development Domain (CDO) and will be empowered to - Leads the analysis of business problems and the translation of business requirements into successful technical solutions and processes to meet business needs. - Analyze business partner’s operations to...

Descriptif du poste Nous sommes actuellement à la recherche d’un **Medical Writer H/F** dont les missions principales seront les suivantes (liste non-exhaustive): - Rechercher des informations auprès des interlocuteurs techniques (rédacteurs médicaux, médecins, statisticiens, équipiers des affaires réglementaires et de pharmacovigilance) -...

THE STERIMED GROUP With 1, employees and 12 factories on 3 continents, STERIMED is the world's leading manufacturer of materials and packaging systems based on renewable resources for the sterilization of medical devices, a market experiencing strong structural growth and an absolute requirement for quality and safety. Sterimed develops, produces,...

As Director/Sr Director, External Innovation - Oncology, you will play a leadership role in IPSEN’s External Innovation group, spearheading efforts to identify, evaluate, and secure Oncology external opportunities (pre-clinical and clinical stage as well as marketed therapeutic assets). It is expected that these efforts will provide direct and visible...