Octapharma Biopharmaceuticals GmbH sucht in eine/n Group Associate Expert Neutralization Testing (m/w/d) (ID-Nummer: 13725564)
Octapharma Biopharmaceuticals GmbH sucht in eine/n Associate Expert (m/f/d) R&D USP (ID-Nummer: 13701993)
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).
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.
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. 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 on medical devices trials.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), ISO 14155 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.Mentoring less experienced team members, acting as subject matter expert for specific topics or additional tasks might be included.
Fachinformatik) Sie bringen einschlägige Erfahrung in der Administration heterogener IT-Systeme mit Sie besitzen fundierte Kenntnisse in der Administration von Servern und Netzwerken Erfahrungen mit Cloud-Technologien, idealerweise Microsoft Azure, sind von Vorteil Zusatzqualifikationen wie Network Engineer Associate, Solutions Architect Expert, Windows Server Hybrid Administrator Associate oder ITIL Foundation sind wünschenswert Sie haben Erfahrung in der Analyse und Optimierung von Prozessen innerhalb der IT-Infrastruktur Sie arbeiten analytisch, strukturiert und zielgerichtet und besitzen ein ausgeprägtes Verständnis für Verfügbarkeit, Betriebssicherheit und effiziente IT-Abläufe.
Fachinformatik)Sie bringen einschlägige Erfahrung in der Administration heterogener IT-Systeme mitSie besitzen fundierte Kenntnisse in der Administration von Servern und NetzwerkenErfahrungen mit Cloud-Technologien, idealerweise Microsoft Azure, sind von VorteilZusatzqualifikationen wie Network Engineer Associate, Solutions Architect Expert, Windows Server Hybrid Administrator Associate oder ITIL Foundation sind wünschenswertSie haben Erfahrung in der Analyse und Optimierung von Prozessen innerhalb der IT-InfrastrukturSie arbeiten analytisch, strukturiert und zielgerichtet und besitzen ein ausgeprägtes Verständnis für Verfügbarkeit, Betriebssicherheit und effiziente IT-Abläufe.
Ihre Aufgaben: Konzeption, Planung und Implementierung von NetScaler Infrastrukturen Konfiguration und Administration von NetScaler Systemen, NetScaler SDX Hardware und NetScaler ADC Betrieb und Optimierung von NetScaler Gateways und Portaltechnologien für sicheren Remote Zugriff Integration von NetScaler Lösungen in bestehende Microsoft Infrastrukturen mit Windows Server, Active Directory und Hyper V Umsetzung von Lastverteilung und Sicherheitskonzepten in Citrix Umgebungen Unterstützung bei Rollout, Migrations und Infrastrukturprojekten in komplexen heterogenen Server und Client Landschaften Berücksichtigung von Netzwerk und Sicherheitskonzepten wie DNSSEC, Zero Trust und MFA Dokumentation der Arbeitseinsätze gemäß Vorgaben des Auftraggebers Ihr Profil: MUST HAVE Mindestens fünf Jahre Berufserfahrung in der Konzeption, Planung und Implementierung von NetScaler Infrastrukturen in der öffentlichen Verwaltung im Zeitraum 01 2016 bis 01 2026 Umfassende Erfahrung mit NetScaler Systemen, NetScaler SDX Hardware, NetScaler ADC sowie NetScaler Gateways und Portaltechnologien Fundierte Kenntnisse in Microsoft Technologien wie Windows Server, Active Directory und Hyper V Gültige Sicherheitsüberprüfung gemäß § 8 Abs. 1 Nr. 3 LSÜG BW zum Zeitpunkt der Angebotsabgabe Mindestens ein gültiges, nicht älter als fünf Jahre altes Zertifikat aus dem Bereich Citrix NetScaler, Citrix Certified Professional Networking, Citrix Certified Expert Networking oder Microsoft Azure Network Engineer Associate mit Nachweis Nachweisbare Projekterfahrung in mindestens drei abgeschlossenen Projekten in der öffentlichen Verwaltung in den letzten fünf Jahren mit dokumentiertem Erfolg NICE TO HAVE Grundkenntnisse in DFSN, ADFS, DNS, DHCP und ADDS Fortgeschrittene Kenntnisse in Netzwerken, Virtualisierung mit Hyper V und VMware sowie Cloud Plattformen wie Azure Grundkenntnisse in Netzwerk und Sicherheitskonzepten wie DNSSEC, Zero Trust und MFA Erfahrung in hybriden Umgebungen unter M365 und Azure sowie mit hybriden und cloudbasierten Infrastrukturen Weitere gültige Zertifikate wie VMware VCP DCV, Microsoft Windows Server Administration Associate oder ITIL Foundation Rahmenparameter: Einsatzort: Stuttgart Laufzeit: nach Zuschlag bis Ende 2026 + Option auf Verlängerung Auslastung: Vollauslastung Ihr GECO-Ansprechpartner freut sich auf Ihre Kontaktaufnahme und über die Zusendung Ihrer aussagekräftigen Projekthistorie sowie Ihrer Honorarvorstellung.
The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge.
The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge.
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 two years of on-site monitoring experienceKnowledge 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.Good command of German and English.Flexibility to business travel up to 60% of working time.Driver’s license class B.
DHL Supply Chain is a world-class company, and we hire only world-class people.People who aren’t afraid to work hard – in fact, people who want to work hard.In this HR Business Partner role: You’ll partner to proactively identify and solve issues You’ll act in both strategic and tactical capacities providing full life-cycle Human Resources support You’ll work closely with business leaders to evolve and embed the people element of the business strategy You’ll take a hands-on approach in monitoring the pulse of our employees to ensure a high level of employee engagement You’ll provide formal and informal coaching to associates at all levels of our business in an impactful, collaborative, and consultative manner You’ll manage the people impacts of organizational change projects aligned to the business Your voice will be heard loud and clear in management circles You’ll deliver results You’ll love it You won’t find an HR opportunity like the one you’ll find with DHL Supply Chain. If you're an exceptional HR expert with a can-do attitude, who's passionate about doing things the right way the first time, join us – the world is waiting for you.Now, here’s what we need from you: 7 years HR experience with 2 years in the Logistics industry At least 5 years in an HR management role Degree in HR or relevant related field Advanced computer proficiency in Microsoft Office Strong labour relations skills and experience working with unions Strong interpersonal skills necessary to communicate at various levels within the organisation
Your responsibilities might include: Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.Collaborate with clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.Assist with periodic review of study files and completeness.Collaborate with CRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.Act as a mentor for less experienced Clinical Trial Coordinators and assist with training and onboarding of new colleagues.May serve as subject matter expert for business processes or lead Clinical Trial Coordinators study teams.May participate in departmental quality or process improvement initiatives.