Wir nehmen uns Zeit für Sie - um gemeinsam mit Ihnen den nächsten Schritt Ihrer Karriere oder Ihres Wiedereintritts ins Berufsleben zu planen. Und stehen Ihnen auch mit einem umfangreichen Angebot an Qualifizierungen und Weiterbildungen zur Seite. Für unseren Kunden, mit Sitz im Großraum Frankfurt, suchen wir ab sofort einen Mitarbeiter im First Level Support (m/w/d).
Wir nehmen uns Zeit für Sie - um gemeinsam mit Ihnen den nächsten Schritt Ihrer Karriere oder Ihres Wiedereintritts ins Berufsleben zu planen. Und stehen Ihnen auch mit einem umfangreichen Angebot an Qualifizierungen und Weiterbildungen zur Seite. Unser Auftraggeber bietet multitechnische Dienstleistungen für Gebäude, Anlagen und Infrastrukturen.
Statistical Analysis & Methodology Independently author Statistical Analysis Plans (SAPs), including drafting in collaboration with cross‑functional partners, pharma statisticians, or from finalized protocols.Implement non‑standard or advanced statistical methodologies, such as:Complex time‑to‑event analysesMMRM and other longitudinal modelsMethods aligned with estimands, including deep understanding of competing policies, assumptions, and analytical implicationsPerform or oversee statistical analyses, ensuring scientific rigor and regulatory compliance.Conduct sample size calculations using SAS or R, and justify design assumptions when engaging with clinical leadership.
Essential Functions Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.Develop contract language, payment language and budget templates as required as applicable to the positionUtilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreementsReport contracting performance metrics and out of scope contracting activities as required.Work with Quality Management to ensure appropriate contract management and quality standards.
Dein Fokus liegt in der Konzeption, Auslegung und Optimierung von Automatisierungs- und Regelungssystemen zur effizienten Entwicklung und Steuerung unserer Anlagen #sort: 200#PES# Erstellen von Spezifikationen und Datenblättern für die Instrumentierung petrochemischer AnlagenPlanen von MSR-Ausrüstung und Auswahl und Auslegung von GerätenSpezifizieren von Messsensoren und Aktoren gemäß P&ID und verfahrenstechnischen VorgabenSpezifikation von Steuerungs- und ProzessleitsystemenErstellen von I/O- und Schnittstellenlisten für Sensorik, Aktorik und DatenaustauschBerechnung von SIL-Loops/Support im Safety ManagementBerechnung von Exi-LoopsKenntnisse in Anwendung und Auslegung von Gas-Chromatografien Planung, Durchführung und Dokumentation von SoftwareupdatesZusammenarbeit mit Verfahrenstechnik, Anlagenbetreiber, Hardware- und Softwareplanung für MSR-TechnikAbgeschlossenes Studium oder technische Weiterbildung im Bereich der Elektrotechnik, Automatisierungstechnik, Verfahrenstechnik, Chemieingenieurwesen oder eine vergleichbare QualifikationMehrjährige Berufserfahrung in der Designer Instrumentierung oder EMSR- Planer (m/w/d) in der chemischen und petrochemischen IndustrieErfahrung in der Entwicklung von Automatisierungs- und ReglungskonzeptenKenntnisse im Explosionsschutzbereich sowie der SIL-Klassifizierung Selbstständige, strukturierte Arbeitsweise, gepaart mit hoher Motivation und TeamfähigkeitBereitschaft zu anteiligen Dienstreisen Gute Deutsch- und Englischkenntnisse in Wort und SchriftEin stark wachsendes Clean Tech- Unternehmen mit einer klaren MissionFlache Hierarchien und eine offene UnternehmenskulturFlexible Arbeitszeiten sowie die Möglichkeit hybrid oder mobil zu arbeitenViel Platz für Eigeninitiative, Gestaltungsspielraum und persönliche und fachliche WeiterentwicklungAbwechslungsreiche & verantwortungsvolle AufgabenBetriebliche Altersvorsorge und eine Bezuschussung zur Berufsunfähigkeitsversicherung Fitnessstudio-KooperationKostenlose Getränke & SnacksAttraktive Gesundheitsangebote am Puls der Zeit
Acting as a strategic partner, you will optimize site experience and performance while fostering strong relationships and sharing medical and scientific information with healthcare providers and caregivers. Key Responsibilities Develop study-specific action plans with research sites to accelerate recruitment and support procedural training.Educate healthcare professionals and their staff on study protocols related to clinical trials.Partner with referral networks to identify potential trial participants.Maintain and analyze customer records to tailor strategies for pre-screening, screening, and enrollment.Complete internal reporting and organize group events to optimize program delivery.Address and manage objections effectively.Stay current with technical knowledge in relevant therapeutic areas.
Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
. • Ensure appropriate trial-specific training of internal and external partners in line with Trial Training Plan. • Develop and maintain relationships with investigational sites and support CRAs in site contacts. • In collaboration with Site Monitoring Lead and CRAs, ensure: o provision of appropriate trial oversight for the trials by monitoring compliance of trial sites and team to GCP, local regulations, customer SOPs, and adherence to trial protocol. o adequate trial supply distribution to sites. o continuous and timely data entry and cleaning, and on time Data Base Lock. o collection of required documents, with timely, complete, and compliant archiving of all relevant documents for the eTMF and CTR Appendices. • Identify risks and contingencies and partner with project leader in problem solving and resolution efforts. • Report to and relate with Trial Leader to provide updates, exchange critical information and share trial conduction information, within regulatory and compliance burdens. • Participate in and actively drive organizational, quality and process improvement initiatives to commence future leading change.
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.
Risk-Based Quality Management: Defines medically critical data/processes and associated risks.Contributes to Integrated Quality and Risk Management Plan (IQRMP).Participates in risk discussions during trial conduct. Clinical Quality Monitoring: Co-authors Clinical Quality Monitoring Plan (CQMP).Aligns CQMP with IQRMP-identified risks and mitigations.
YOUR ROLE Responsible for growing the long-term value and performance of the entire bread category by developing a category strategy to analyze and optimize the profitability of the product line Managing and coaching 2 Product Leaders Supporting OpCo’s in making strategic product choices, acting as an internal advisor and decision driver for the category Maintaining the standard portfolio, developing and maintaining strategic brands and concepts across multiple countries Leading innovations projects from business case to market introduction by customers, end-to-end (E2E) Building solid bridges between the group, organization and OpCo’s and co-create with cross functional colleagues Identifying additional markets to launch and defining with OpCo’s, M&A and strategic partnership options to address adjacent growth opportunities and complete the category portfolio Collaborating intensively with the other Global Category Managers, Product Leaders, the Commercial Development Manager and the OpCo’s Member of the Marketing/R&D Management Team and reporting to the Group Marketing/R&D Director YOUR PROFILE BSc/MSc degree in Marketing, Business Administration, Food Science & Technology or similar Relevant experience in international B2B marketing, category management in senior management roles, preferably in the international food ingredients industry Capable of understanding the technical aspects of products like functional ingredients such as enzymes, emulsifiers or other raw materials Strong project management skills by leading and participating in cross-functional teams and by building bridges between global and local teams Good understanding about trends, market and customer requirements and able to translate these into plans and actions Comfortable working in an international matrix organisation with different stakeholders, markets and cultures and willingness to travel in Europe; Zeelandia offers the possibility for hybrid working in combination with working in the office in Zierikzee or any other Zeelandia office or plant in Europe Excellent communication and presentation skills in English Personal skills: leadership, well organised, analytically strong, drive for innovation, setting priorities, convincing and taking decisions priorities, convincing and taking decisions CONTACT If you are interested in this position, please contact Jakob Jan Verbraak from our IFR-A partner DUPP, telephone: +31 317-468686 / +31 6-51820349 or apply through their website www.dupp.nl or e-mail your written application to info@dupp.nl.