Prüfung von Sponsoring-Anfragen auf FSA-Konformität, Transparenzvorgaben und interne Standards Herstellung vollständiger Dokumentation gemäß Lilly-ProzessenAbgleich der Anfragen mit strategischen Prioritäten der BrandsBudgetmonitoring sowie Erstellung monatlicher Reports für Business, Finance und Compliance.Enge Abstimmung mit Brand Teams, Medical, Legal und ComplianceAnsprechpartner für interne Stakeholder und externe Dienstleister (inkl.
Verwaltung der betrieblichen Altersvorsorge in der Entgeltabrechnung Bewertung der Lohnsteuerpauschalierung von geldwerten Vorteilen Kontenabstimmung der Personalkonten im Rechnungswesen Erstellung von Auswertungen und Reports ------ Deine Qualifikation Erfolgreich abgeschlossene kaufmännische Ausbildung und/oder Weiterbildung zum/zur Lohn- und Gehaltsbuchhalter/in, Steuerfachangestellten oder eine vergleichbare Qualifikation Einschlägige Berufserfahrung in der Entgeltabrechnung Fundierte Kenntnisse im Lohnsteuer- und Sozialversicherungsrecht Hohe Dienstleistungsorientierung sowie eine proaktive und eigenständige Arbeitsweise Engagement und Teamgeist: du übernimmst gerne Verantwortung, bringst deine Ideen ein und trägst so zum Erfolg des Teams und des Unternehmens bei Sicherer Umgang mit MS Office ------ Das bieten wir Dir Professionelle Einarbeitung und begleiteter Onboarding-Prozess Mobiles Arbeiten JobRad und Corporate Benefits Kostenlose Getränke Firmenevents und Teambildungsmaßnahmen ------
Payroll Manager (m/w/d) Ihre Aufgaben: Full responsibility for the accurate and timely end-to-end payroll processing for a German legal entity Ensure compliance with all applicable German labor laws, tax regulations, and social security requirements Close collaboration with HR and Finance regarding salary adjustments, benefits, and other compensation-related changes Manage and oversee external payroll service providers, ensuring quality and performance standards Coordinate with external pension and benefits providers, including data exchange, reporting, and audit support Prepare regular and ad-hoc payroll reports for internal and external stakeholders Support internal and external audits, including reconciliations and resolution of discrepancies Review quarterly tax filings and perform payroll-related reconciliations Identify and implement process improvements and automation initiatives to enhance efficiency and accuracy Act as the primary point of contact for employees regarding payroll-related inquiries Provide guidance on time tracking and approval workflows within the Workforce Management system Ensure proper documentation and maintenance of payroll records Ihr Profil: Bachelor’s degree in Accounting, Finance, Business Administration, or a comparable qualification Minimum of 5 years’ experience in payroll administration, with a strong focus on German payroll In-depth knowledge of German payroll regulations, tax law, and compliance requirements Experience working with external payroll vendors Strong proficiency in payroll systems and HRIS/time tracking tools Analytical mindset with strong attention to detail and accuracy Highly organized, reliable, and able to handle sensitive information with discretion Fluent in German and English Preferred Qualifications Experience with equity-based compensation, bonus schemes, or international assignments Familiarity with internal control frameworks and compliance requirements (e.g., SOX) Advanced Excel skills and experience in payroll data reporting and audit preparation Strong communication skills with the ability to work both independently and collaboratively Ability to manage a diverse workload in a deadline-driven environment Ihre Vorteile: You can look forward to a secure, future-oriented position with performance-based compensation and attractive working conditions.
Payroll Manager (m/w/d) Ihre Aufgaben: Full responsibility for the accurate and timely end-to-end payroll processing for a German legal entity Ensure compliance with all applicable German labor laws, tax regulations, and social security requirements Close collaboration with HR and Finance regarding salary adjustments, benefits, and other compensation-related changes Manage and oversee external payroll service providers, ensuring quality and performance standards Coordinate with external pension and benefits providers, including data exchange, reporting, and audit support Prepare regular and ad-hoc payroll reports for internal and external stakeholders Support internal and external audits, including reconciliations and resolution of discrepancies Review quarterly tax filings and perform payroll-related reconciliations Identify and implement process improvements and automation initiatives to enhance efficiency and accuracy Act as the primary point of contact for employees regarding payroll-related inquiries Provide guidance on time tracking and approval workflows within the Workforce Management system Ensure proper documentation and maintenance of payroll records Ihr Profil: Bachelor’s degree in Accounting, Finance, Business Administration, or a comparable qualification Minimum of 5 years’ experience in payroll administration, with a strong focus on German payroll In-depth knowledge of German payroll regulations, tax law, and compliance requirements Experience working with external payroll vendors Strong proficiency in payroll systems and HRIS/time tracking tools Analytical mindset with strong attention to detail and accuracy Highly organized, reliable, and able to handle sensitive information with discretion Fluent in German and English Preferred Qualifications Experience with equity-based compensation, bonus schemes, or international assignments Familiarity with internal control frameworks and compliance requirements (e.g., SOX) Advanced Excel skills and experience in payroll data reporting and audit preparation Strong communication skills with the ability to work both independently and collaboratively Ability to manage a diverse workload in a deadline-driven environment Ihre Vorteile: You can look forward to a secure, future-oriented position with performance-based compensation and attractive working conditions.
Objektleiter (m/w/d) Für unseren Kunden aus der technischen Dienstleistungsbranche suchen wir zur Unterstützung und zum schnellstmöglichen Zeitpunkt Sie als: Objektleiter (m/w/d) Ihre Vorteile: Anstellung in einem unbefristeten Arbeitsverhältnis Schneller und unkomplizierter Einstieg Urlaubs- und Weihnachtsgeld Individuelle Betreuung als Mitarbeiter (m/w/d) Zukunftsorientierte Einsätze Ihre Tätigkeiten: Betreuung von Objekten und Überwachung der vereinbarten InstandhaltungsleistungenErstellung von Reports und Vorbereitung des BerichtswesensPlanung, Organisation und Steuerung von Instandsetzungs- und Wartungsarbeiten zur Sicherstellung der Betriebsbereitschaft des ObjektesBetreuung und Koordination von externen Dienstleistern und FremdfirmenOrganisation der Personalplanung sowie Arbeitseinsätze Ihre Qualifikationen: Abgeschlossene Qualifikation als Meister oder Fachwirt im Bereich Elektrotechnik, Haustechnik oder vergleichbaresLangjährige Berufserfahrung als Objektleiter (m/w/d) in der technischen Objektbetreuung oder GebäudetechnikGute Deutschkenntnisse in Wort und SchriftBesitz eines PKW-FührerscheinsEigenständigkeit und eine strukturierte ArbeitsweiseEinsatzbereitschaft und Kundenorientiertes Auftreten Ihr Kontakt zu Hofmann: Sie möchten als Objektleiter (m/w/d) arbeiten?
Erstellen der Einweisungsunterlagen Pflege unserer BesprechungsräumeFühren und Verwalten von Lieferantenbeziehungen, rund um Lebensmittel- und Getränkelieferungen, Büromaterial, Arbeitskleidung in Zusammenarbeit mit dem zentralen Office ManagementBestellung von Arbeits- und Betriebsmittel, Verbrauchsmaterial und ErsatzteilenUnterstützung des Termin- und Kommunikationsmanagement für den BetriebsleiterErstellen von Ausfuhrscheinen, werksinternen Anträgen und Dokumenten sowie Unterstützung bei der Dokumentenablage und -lenkungDienstbotengänge innerhalb und außerhalb des WerkesUnterstützung bei der Reisekostenabrechnung sowie Erstellen von einfachen Reports (z. B. Schichtlisten nach Vorgabe)Unterstützung bei der Urlaubsplanung des TeamsAusbildung oder Studiengang im Bereich Administration, Kommunikation, Sekretariat oder eine entsprechende Qualifikation im Office ManagementMindestens 3 Jahre Berufserfahrung als Office Manager, Front Office Manager oder Administrative Assistant (m/w/d) oder vergleichbaremAusgeprägtes Koordinations- und Organisationsgeschick sowie proaktive ArbeitsweiseSehr gute Selbstorganisation und Umgang mit ZeitmanagementSicherer Umgang mit den gängigen MS Office ProgrammenSehr gute Deutsch- und Englischkenntnisse in Wort und Schrift (weitere Sprachen sind von Vorteil)Ein stark wachsendes Start-Up mit einer klaren MissionFlache Hierarchien und eine offene UnternehmenskulturViel Platz für Eigeninitiative/Gestaltungsspielraum sowie persönliche und fachliche WeiterentwicklungAbwechslungsreiche und verantwortungsvolle AufgabenBetriebliche Altersvorsorge und eine Bezuschussung zur BerufsunfähigkeitsversicherungFitnessstudio-KooperationKostenlose Getränke & SnacksAttraktive Gesundheitsangebote am Puls der Zeit
We are seeking a Principal Medical Writer to support full Clinical Study Report (CSR) writing for Phase 1 , protocol development, and preparation of regulatory modules (2.7.1/2.7.2) . This role requires strong writing skills and attention to detail to ensure high-quality, inspection-ready deliverables.
Ensure overall contract management, including review and approval of external service provider (ESP) contracts, change orders and ensure services are delivered per contract.Act as primary company contact for assigned trial at the country level and ensures local/country team is tracking project progress against planned timelines and monitors patient recruitment rate to ensure that target enrollment will be met across the allocated countries.Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to analyze trial progress. Participates in preparation for and conduct of Health Authority (HA) inspections and internal Quality Assurance audits.Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target.Deliver competent vendor management at the country level to support the study and may submit requests for vendor services and support vendor selection.Contribute to patient understanding of protocol and patient safety by contributing to the review of country specific informed consent in accordance with procedural document/templates.Ensure trial subject safety in that all AEs/SAEs/PQCs are reported within the required reporting timelines and documented, as appropriate.Ensure Inspection readiness by maintaining complete, accurate and timely data and essential documents in systems utilized for trial management (e.g.
Key Responsibilities: Receptionist Greet and welcome visitors, ensuring a positive first impressionManage incoming calls and direct them appropriatelyMaintain an organized and tidy reception areaCoordinate visitor access and issue visitor badgesProvide high-quality customer service and assist with inquiries Administrative Support Assist with scheduling and coordination of meetings and appointmentsManage incoming and outgoing mail, including sorting and distributing packagesMaintain accurate records and files, including office supplies inventoryPrepare and distribute internal communications, memos, and announcementsAssist with travel arrangements and expense reimbursements Workplace Operations Ensure meeting rooms are set up and equipped with necessary technologyAssist with event coordination, including room bookings and catering arrangementsLiaise with vendors and suppliers for office supplies and maintenance requestsCoordinate office equipment repairs and maintenanceAssist with access card management and security procedures Health and Safety Monitor and report any health and safety hazards or incidentsEnsure compliance with workplace safety policies and proceduresConduct regular inspections of common areas and report maintenance issuesAssist with emergency response protocols and evacuation procedures Qualifications: High school diploma or equivalent (additional education/training is a plus)Proven experience in a receptionist or administrative roleStrong interpersonal and communication skillsExcellent customer service orientationProficient in using office software and equipment (e.g., Microsoft Office Suite, phone systems)Ability to prioritize and multitask in a fast-paced environmentAttention to detail and strong organizational skillsUnderstanding of basic health and safety regulations What we can do for you: At JLL, we make sure that you become the best version of yourself by helping you realise your full potential in an entrepreneurial and inclusive work environment.
. • 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.
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.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 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.
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).
Participates in planning and reviewing medical sections of Clinical Trial Reports. Qualifications Medical degree from an accredited and internationally recognized medical school. Typically requires a minimum of 5-7 years' experience in clinical medicine.