Rare Disease Clinical Research Physician

Emploi pas sur LinkedIn

🕒 il y a 3 mois

🇮🇹 Italie – Télétravail

💵 €68 480 / an

⏰ Temps Plein

🟡 Intermédiaire

🟠 Senior

🧪 Chercheur Clinique

👻 Score fantôme 9%

Ce que ça veut dire : la probabilité que personne ne recrute vraiment pour cette offre.Comment le lire : 60 % ou plus, on pense que c'est une offre fantôme. Un score plus bas est moins inquiétant.Pourquoi ce score :

• Ouverte depuis 92 jours.
• Les offres de cette entreprise sont généralement pourvues en 58 jours.

Postuler Maintenant

Trouver des Emplois à Distance Similaires

Chiesi Group

Site WebLinkedInTous les Emplois

5001 - 10000 employés

🏥 Santé

🏭 Fabrication

💊 Pharmaceutique

Healthcare • Manufacturing • Pharmaceuticals

Le Groupe Chiesi est une entreprise pharmaceutique mondiale axée sur la recherche, le développement et la commercialisation de médicaments innovants. Reconnu pour son engagement à améliorer la vie des patients, l'entreprise se spécialise dans des domaines tels que les maladies respiratoires, les soins spécialisés et les maladies rares. Le Groupe Chiesi met l'accent sur la durabilité et la responsabilité d'entreprise, avec pour objectif d'améliorer la santé et le bien-être à l'échelle mondiale tout en étant dédié à la gestion environnementale.

Description

• Provide scientific and technical leadership for analytical method development, method qualification and validation, analytical control strategy, comparability, technology transfer, stability strategies, and lifecycle activities • Lead an extended technical team and align analytical CMC deliverables with project objectives, regulatory expectations, quality requirements, timelines, and budget • Build and retain product knowledge within GRD • Support effective decision-making and external partner oversight • Establish fit-for-purpose ways of working for rare disease development • Act as subject matter expert for analytical and CMC technical areas involving biological products such as protein therapeutics • Lead or contribute to CMC strategies from candidate selection through clinical supply, technology transfer, process characterization, validation, regulatory submission, launch, and lifecycle management • Provide guidance on expression systems, cell line development, clone selection, cell banks, media and feed development, upstream process development, harvest, clarification, purification, impurity clearance, scale-up, and process control • Translate scientific and analytical data into risk-based CMC strategies and development decisions • Lead identification and management of critical quality attributes and key product quality attributes • Drive phase-appropriate control strategies covering process parameters, in-process controls, release testing, characterization, comparability, specifications, and lifecycle knowledge management • Lead technical risk assessments, process change assessments, comparability strategies, troubleshooting, investigations, deviations, CAPAs, and continuous improvement activities • Lead technical discussions with internal stakeholders, CDMOs, CROs, academic partners, and external consultants • Support selection, evaluation, and oversight of external development and manufacturing partners • Contribute to technical and regulatory documentation, business development and due diligence assessments, and GRD CMC ways of working

🎯 Exigences

• A university degree in biotechnology, biochemistry, chemistry, biology, pharmacy, engineering, or a related scientific discipline • Advanced degree is an advantage • Significant experience in analytical method development, method qualification and validation for biologics • Experience with analytical control strategy, stability testing, comparability, technology transfer, or lifecycle management within CMC development • Strong scientific understanding of analytical techniques relevant to biologics development • Understanding of assay performance, robustness, method lifecycle, data interpretation, and regulatory expectations for validated methods • Strong understanding of GMP, regulatory expectations, quality systems, and development requirements for clinical and/or commercial manufacturing • Experience working with CDMOs, CROs, external partners, or outsourced development and manufacturing models • Ability to translate complex technical information into clear recommendations, fit-for-purpose plans, and practical decisions • Experience leading technical discussions, coordinating cross-functional activities, and influencing stakeholders in a matrix environment • Excellent written and verbal communication skills in English • Proactive, solution-oriented, and comfortable taking responsibility when priorities evolve

🏖️ Avantages

• Annual bonus scheme, subject to company and individual performance • Pension • Private medical insurance • Wellbeing programme • Flexible benefits programme • Comprehensive healthcare programs • Work-life balance initiatives • Relocation support • Flexible working arrangements • Remote work options • Tax assistance services for foreign colleagues • Access to resources and training • Performance bonuses

📊 Vérifiez votre score de CV pour ce poste

Améliorez vos chances d'obtenir un entretien en vérifiant votre score de CV avant de postuler.

Télécharger le CV