TRUECARE GmbH sucht in Frankfurt am Main eine/n Key Account Manager (w/m/d) (ID-Nummer: 13842488)
Novoferm Vertriebs GmbH sucht in Mitteldeutschland / Frankfurt eine/n Key Account Manager (m/w/d) (ID-Nummer: 13836444)
ProTect Dienstleistungs GmbH sucht in eine/n Key Account Manager Österreich (all genders) (ProTect) (ID-Nummer: 13849269)
ATLAS Vertriebsservice GmbH sucht in eine/n Key Account Manager / Organisationsbetreuer (m/w/d) (ID-Nummer: 13798351)
Stellenbeschreibung Unser Mandant ist ein international tätiger Technologieanbieter im Bereich digitaler Netzwerke in der Tourismusbranche, wir suchen einen erfahrenen Key Account Manager (m/w/d) für den strategischen Vertrieb im Hospitality-Segment. Key Account Manager (m/w/d) IT Raum Frankfurt / Offenbach am Main Ihre Aufgaben: Sie betreuen bestehende Key Accounts aus der Hotel- und Hospitalitybranche und entwickeln diese partnerschaftlich weiter, um langfristige Geschäftsbeziehungen zu stärken und zusätzliche Umsatzpotenziale zu erschließen.
DELTA Electronics (Germany) GmbH sucht in eine/n Key Account Manager – Telecom Solutions (m/w/d) (ID-Nummer: 13867583)
Würth Deutschland sucht in eine/n Technischer Key Account Manager Bereich Brandschutz (m/w/d) (ID-Nummer: 13747952)
Wir sind Ihr kompetenter und verläßlicher Partner auf der Suche nach Ihrem Traumjob, kurzfristig, langfristig, zur Übernahme oder zur Vermittlung. Key Account Manager m/w/d Vollzeit Key Account Manager m/w/d in Frankfurt Die Bader + Kara GmbH Frankfurt sucht ab sofort einen Key Account Manager m/w/d intern in der Zeitarbeit, zu Ihren Aufgaben zählen u.a.
PCT Performance Chemicals GmbH sucht in eine/n Key Account Manager / Objektberater (m/w/d) (ID-Nummer: 13664831)
Elis Deutschland sucht in eine/n Key Account Manager (m/w/d) New Sales (ID-Nummer: 13836423)
Etengo AG sucht in Mannheim, Frankfurt am Main, Düsseldorf, Köln, Berlin, München eine/n (Senior) Key Account Manager (m/w/d) mit Führungsperspektive (ID-Nummer: 13806639)
Für den Bereich Spezialpharmazeutika suchen wir dich zum schnellstmöglichen Zeitpunkt als Key Account Manager (m/w/d) im Bereich der Uro-Onkologie. deine aufgaben: Sei ganz vorne mit dabei! Regelmäßige Besuche und fachliche Beratung von ausgewählten Ärzt/innen (Schwerpunkt Urologie und Onkologie/Hämatologie) sowie von speziellen Kundengruppen (Qualitätszirkel, Netzwerker, etc.) gehören zu deinen Hauptaufgaben.
PharmD, PhD, or MD – other doctoral degrees may be considered).Experience in the area of dermatology and/or autoimmune diseases preferred.Previous experience as MSL or other medical function prerequisite.Field experience is a plus.Flexibility, diplomacy, and ability to manage expectations.Problem solving and entrepreneurial skills.Ability to travel frequently with overnight stays (e.g. thought leader visits, internal client meetings, medical meetings and congresses, and training meetings).
For this important task, they are looking to hire an ambitious salesperson. YOUR ROLE Reporting directly to the General Manager of the German subsidiary and the Head of Sales Europe (dotted line), you are responsible to implement Wismettac’s sales strategy in the German retail and/or foodservice market With the objective of growing the sales revenue, you systematically work through the market by defining and evaluating potential profits and deriving the necessary next steps By identifying, approaching, and acquiring key customers, you build and maintain a broad customer base You set up and implement solid sales structures and prepare to further expand the German business YOUR PROFILE You have a proven track-record in sales functions and experience in launching new food products in Germany You have a solid network within and a profound knowledge of the German retail and/or foodservice sector Being a self-confident, determined, and proactive self-starter, you thrive on challenges and ambitious sales targets and are willing to go the extra-mile THE OFFER FOR YOU Wismettac’s founding philosophy is to “bring the food of the world to Japan and the food of Japan to the world” and thus enrich the lives of people through food.
On behalf of an internationally operating organization, we are seeking an experienced Payroll professional to take full ownership of payroll operations for an international entity and serve as the key contact for all payroll-related matters. 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.
On behalf of an internationally operating organization, we are seeking an experienced Payroll professional to take full ownership of payroll operations for an international entity and serve as the key contact for all payroll-related matters. 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.
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. Qualifications Registered Nurse, other healthcare professional, or Clinical Research Associate (CRA) required.High flexibility to travel (including internationally if needed).Bachelor’s degree (BA/BS) in Health Sciences or related field, or equivalent qualifications.Located in Germany with fluency in German and English languages.1–2 years of relevant direct experience in working with research sites.Clinical competence in the therapeutic area.Excellent interpersonal and communication skills.Strong written and verbal communication skills.Ability to work independently and coordinate across multiple functions.Solutions-oriented approach and positive attitude.Strong customer service orientation and collaborative mindset.Demonstrates empathy and cultural awareness.Upholds the values of IQVIA and the CTE group.
Applicants should have: A university degree in a health care or other scientific discipline or a vocational education in the medical field.A completed advanced training in clinical research is mandatory.Fluent written and verbal communication skills in German on at least C1 level, including good command of English is mandatory.Flexibility to regular business travel up to 40-60% of the working time and a driving license class B.Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.Excellent organizational and problem-solving skills.Effective time management skills and ability to manage competing priorities.Ability to establish and maintain effective working relationships with coworkers, managers and clients.Availability to start on 16.
Innovation Facilitation: Provide standard components and tools that enable application teams to innovate rapidly without reinventing the wheel. Technical Shielding: Abstract and manage complex technical challenges, allowing application teams to focus on application-specific functionalities. Collaboration: Work closely with cross-functional teams to understand their needs and integrate GenAI solutions seamlessly.
Job Overview: As an Associate Director, Biostatistics, with regional/site presence, you will manage a team of Biostatistics staff and fulfil the role of site head or functional head within a site. You will provide direction and guidance in carrying out project assignments, interfacing with clients and other internal departments, and applying advanced statistical methods to project work.
. • Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines • Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables • Use and promote the use of established standards, SOP and best practices • Provide training and mentoring to SP team members Requirements: • Bachelor's Degree in Maths, Computer science, Statistics, or related field • 7+ years’ Statistical Programming experience within the Life Science Industry • Strong Efficacy experience • Advanced knowledge of statistics, programming and/or clinical drug development process • Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro • Language • Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM) Join IQVIA to see where your skills can take you • Global exposure • Variety of therapeutic areas • Collaborative and supportive team environment • Access to cutting-edge and innovative, in-house technology • Excellent career development and progression opportunities • Work-Life Balance, with a strong focus on a positive well-being Unleash your potential!
Job Ticket, Corporate Benefits, Fahrradleasing, Familienservice, Zuschuss zu Kinderbetreuungskosten und Altersvorsorge ab dem ersten Tag • Regelmäßige Charity- und Mitarbeiterevents, um das WIR-Gefühl zu stärken und ein firmenweites Netzwerk aufzubauen Das machst Du bei uns: • Du entwickelst eigenverantwortlich kundenspezifische Immobilienstrategien für internationale und nationale Großunternehmen • Du bist Key-Account Manager für internationale Kunden in Frankfurt und Umgebung und strategischer Partner auf C-Level • Du berätst unsere Kunden umfassend bei deren Immobilienstrategie – von Portfolio-Optimierung bis Workplace Transformation • Du führst eigenständig Verhandlungen von Mietverträgen und begleitest komplexe Mietvertragsabschlüsse • Du koordinierst den gesamten Anmietungsprozess und die strategische Abstimmung mit technischen und juristischen Beratern • Du analysierst kontinuierlich und proaktiv den Frankfurter Büroimmobilienmarkt auf Chancen und Risiken • Du arbeitest eng mit unterschiedlichen JLL-Einheiten zusammen, wie Project & Development Services und Workplace Solutions • Du akquirierst eigenständig neue Mandate und Kunden • Du repräsentierst JLL auf Branchenevents und Networking-Veranstaltungen • Du mentorst Junior-Kollegen in ihrer fachlichen und persönlichen Entwicklung Das wünschen wir uns: • Ein abgeschlossenes Studium mit immobilienwirtschaftlicher Ausrichtung, BWL, Wirtschaftsgeographie oder eine Ausbildung als Immobilienkaufmann/-frau mit entsprechender Weiterbildung • Mindestens 5 Jahre Berufserfahrung im Office Leasing, Tenant Representation oder im gewerblichen Immobilienvertrieb • Nachweisbare Erfolge in der Betreuung von Firmenkunden und der Abwicklung komplexer Transaktionen • Fundierte Kenntnisse des Frankfurter Büroimmobilienmarktes • Etabliertes Netzwerk zu relevanten Marktteilnehmern (Mieter, Vermieter, Entwickler) • Ausgeprägtes analytisches Talent für komplexe Zusammenhänge • Verhandlungssichere Deutsch- und Englischkenntnisse in Wort und Schrift • Herausragende Akquisitionsstärke und nachgewiesene Erfolge im eigenständigen Aufbau von Kundenbeziehungen • Exzellente Team- und Kommunikationskompetenzen sowie eine hohe Dienstleistungsorientierung • Unternehmerisches Denken und Verhandlungsgeschick auf höchstem Niveau Wir sind neugierig darauf Dich kennenzulernen!
Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations.Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in Sponsor clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head.Ensures timely preparation of local Master CSA (including site budget) and amendments as needed.Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations.Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs.Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction).Sets up and maintains the study in CTMS at study country level as well as local websites as required by local laws and regulations.Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans.Reviews monitoring visit reports (as required and following Sponsor SOPs) and pro-actively advices the monitor(s) on study related matters.Performs any required co-monitoring, Accompanied Site Visits/training visits with study CRAs.Proactively identifies risks and facilitates resolution of complex study problems and issues.Organises regular Local Study Team meetings on an agenda driven basis.Actively works towards achieving good personal relationships with all Local Study Team members, sites’ staff and global stakeholders.Reports study progress/update to the Global Study Associate Director/ Global Study Team including SMM Lead.Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary.Develops, maintains and reviews risk management plan on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed.Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable.Plans and leads National Investigator meet Ensures that all study documents are ready for final archiving and completion of local part of the eTMF.Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and QA.Provides input to process development and improvement.Provides regular information to Line Managers at country level on study/ies and planned study milestones/key issues.Updates Line Managers about the performance of the CRAs/CSAs.Ensures that study activities at country level comply with local policies and code of ethics.Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.Ensures compliance with Sponsor´s Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment).Collaborates with local Medical Affairs team.Supports SMM in different initiatives (local, regional or global) as agreed with the SMM Line Management.