Porsche Consulting GmbH sucht in eine/n Senior Expert Produktstrategie & Modularisierung (all genders) mit Fokus auf Automotive & Industrial Goods (ID-Nummer: 10657816)
Porsche Consulting GmbH sucht in eine/n Senior Expert Cost & Value Engineering (all genders) mit Fokus auf Automotive & Industrial Goods (ID-Nummer: 9281759)
🎓 Qualifications & Experience Bachelor’s degree in a related field (required). 5+ years of site contracting experience within a sponsor or CRO, including demonstrable experience as an international contract expert. Equivalent combinations of education, training, and experience will be considered. Strong negotiation and communication skills, with the ability to challenge and influence.
Ihre Zukunft beginnt heute Die Arbeitswelt von morgen braucht Experten wie Sie – Menschen mit dem Mut, Neues zu gestalten. Bei JLL finden Sie nicht nur einen Job, sondern eine Berufung, die Sie persönlich und beruflich erfüllt.
. • Independently author and review trial-level documents. • Act as subject matter expert on site management and monitoring topics. • Join and presents at global/regional/local Trial Team meetings and Investigator Meetings
Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits.Supporting the development of a subject recruitment plan.Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.Collaborating with experts on study sites and client representatives. Qualifications: University Degree in life science or other scientific discipline or apprenticeship in health care.Minimum of one year of on-site monitoring experience, alternatively miminum one year experience as Study Coordinator/CTC etc.Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment.Fluent command of German and English.Flexibility to business travel up to 60% of working time.Driver’s license class B.
Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits.Supporting the development of a subject recruitment plan.Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.Collaborating with experts at study sites and with client representatives.Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices).Mentoring of less experienced team members, support as subject matter expert for specific topics or additional tasks might be included.
Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits.Supporting the development of a subject recruitment plan.Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.Collaborating with experts at study sites and with client representatives.Depending on client model there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices).
Sie führen den Sales Cycle end-to-end und steuern funktionsübergreifende Expert-Teams vom ersten Kontakt bis zum Vertragsabschluss. Was Sie gestalten Pipeline entwickeln & Chancen erkennen Sie identifizieren gemeinsam mit unserem Business Development Team High-Value-Chancen.
Allocate direction, advice, and intellectual leadership to clients and delivery teams. Form pursuit teams for larger engagements with the appropriate experts from the broader IQVIA organization during pre-sales, sales and delivery phases. Oversee the delivery in a Principal-in-Charge (PIC) role for projects in your area of expertise, with full responsibility vis-à-vis our clients for quality, time and budget.
As such you will manage cross-functional trial teams at the customer, acting as that accountable point for delivery and quality whilst maintaining financial control. You will be supported by domain experts in every function, enabled by best-in-class technology and data analytics. 1. Role purpose As Clinical Trial Leader, you will act as the primary driver of study execution and be accountable for the operational performance of assigned clinical trials across preparation, initiation, conduct, close-out, and reporting.
Zur Verstärkung unseres Teams suchen wir einen Head of Technical Experts Digital (m/w/x) ------ Ihre Aufgaben Fachliche und disziplinarische Führung des Teams On-Site Customer Enablement Digital WorkflowsWeiterentwicklung, Schulung und Förderung der Mitarbeitenden im TeamDurchführung und Nachverfolgung von Zielvereinbarungs- und FeedbackgesprächenCoaching der On-Site Customer Enablement Manager zur professionellen Lösung anspruchsvoller KundensituationenSicherstellung der erfolgreichen Umsetzung der verkauften digitalen Produkte und Workflows bei Kunden, sowie Ressourcenplanung.Unterstützung des Außen- und Innendienstes bei komplexen Kunden- und Workflow-HerausforderungenAufbau, Pflege und Weiterentwicklung nachhaltiger KundenbeziehungenEnge Zusammenarbeit mit internen Schnittstellen wie Kundenservice Digital, Produktmanagement & Marketing, sowie weiteren Teams im Bereich Customer Success & Growth ManagementAktive Mitwirkung an strategischen Themen und der Weiterentwicklung zukunftsorientierter After-Sales-Prozesse, sowie des Service- und SupportangebotsTeilnahme an Fortbildungsveranstaltungen, Messen und KongressenFörderung einer teamübergreifenden Zusammenarbeit zwischen Innen- und Außendienst ------ Ihr Profil Qualifikation Zahntechnische oder zahnmedizinische Ausbildung oder betriebswirtschaftliche Ausbildung bzw.