LAVORO HEAD OF REGULATORY AFFAIRS PARMA, EMILIA ROMAGNA
(18 offerte di lavoro)
Listado de trabajos de Head of regulatory affairs en Parma, Emilia romagna
Senior global regulatory affairs project manager
Experience required 5 years in regulatory with good knowledge of drug development and regulatory procedures education at least bachelor’s degree in life sciences...
Head of global complaints, product quality risk & incident management
In-depth knowledge of regulatory requirements and industry standards related to product quality and complaints management (e... experience in multiple risk management...
Head of global quality life cycle
Deep understanding of quality management systems, compliance standards, and regulatory requirements within the pharmaceutical sector... main responsibilities integrated...
Head of clinical project management
Strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements, and cro/vendor management... promote a mindset of accountability, continuous improvement...
Excellent knowledge of the clinical trials settings... regulatory compliance: ensure all documents comply with the applicable regulatory guidelines and company...
Global r&d demand and business knowledge data scientist
Support the definition and periodic refresh of the r&d strategy through the collection and elaboration of both qualitative and quantitative information...
Basic knowledge of project management comprehensive understanding of drug development process... purpose of the role: improving the lives of patients...
Senior clinical research physician non-obstructive respiratory diseases
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... they will drive the preparation of documents for regulatory submissions...
Sr. director, r&d external opportunities
We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors... leadership and coordination - mobilize...
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Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... engage with regulatory authorities, external experts, and key...
We believe that the success of chiesi is built and shaped by our people and our strong set of shared values and behaviors... she/he will partner with customer facing...
Principal extractable and leachable scientist
Deep knowledge of gmp/cgmp and guidelines (ich, emea, pqri, health canada) related to the pharmaceutical development of inhalation products...
Clinical research physician copd/bronchiectasis
Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... clinical section of the investigator’s brochure, protocols and clinical...
Intern - computational jr chemist / bioinformatician
Basic knowledge of python (e... participating in the analysis and interpretation of computational results, under the guidance of senior scientists...
Modeling & simulation scientist
Author, review or approve pharmacometrics reports and related sections of regulatory documents; participate in meetings with clients and regulatory agencies...
Scientist - in vitro pharmacology - respiratory targeted drug discovery
Maintain detailed and accurate records of experiments and results... design, develop, and execute in vitro pharmacological assays to evaluate the efficacy and mechanism...
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Vuoi trovare lavoro?
