Heraeus Holding GmbH sucht in eine/n Senior Manager (m/w/d) Corporate Development & Technology (ID-Nummer: 14548805)
Instone Real Estate Development GmbH sucht in eine/n BIM Manager (m/w/d) (ID-Nummer: 14509688)
42Watt sucht in eine/n Sales Manager Wärmepumpen (gn) - Außendienst, Region Mainz – Wiesbaden - Frankfurt (ID-Nummer: 14594125)
EY-Parthenon Financial Services GmbH sucht in eine/n EY-Parthenon Manager Strategy Commercial Due Diligence & Value Creation (Financial Services) (w/m/d) (ID-Nummer: 14591479)
EY Deutschland sucht in eine/n Manager Umsatzsteuer / Indirect Tax (Financial Services) (w/m/d) (ID-Nummer: 14575244)
Arup Deutschland GmbH sucht in Düssseldorf, Frankfurt am Main eine/n (Senior) Project Manager - Corporate Real Estate (m/w/d) (ID-Nummer: 14164207)
DAIKIN Airconditioning Germany GmbH sucht in eine/n Area Sales Manager (m/w/d) Kaltwasser - Großraum München, Stuttgart oder Frankfurt (ID-Nummer: 14520905)
Wir suchen nach Mitarbeitern (m/w/d) aus den Bereichen: Account Manager (m/w/d), Sales Consultant (m/w/d), Vertriebsmitarbeiter im Außendienst (m/w/d), Key Account Manager (m/w/d), Gebietsverkaufsleiter (m/w/d), Vertriebsaußendienstmitarbeiter (m/w/d), Account Executive (m/w/d), Sales Executive (m/w/d), Business Development Manager (m/w/d) JETZT BEWERBEN
Wir suchen nach Mitarbeitern (m/w/d) aus den Bereichen: Account Manager (m/w/d), Sales Consultant (m/w/d), Vertriebsmitarbeiter im Außendienst (m/w/d), Key Account Manager (m/w/d), Gebietsverkaufsleiter (m/w/d), Vertriebsaußendienstmitarbeiter (m/w/d), Account Executive (m/w/d), Sales Executive (m/w/d), Business Development Manager (m/w/d) JETZT BEWERBEN
Unser Bereich Advisory Financial Services ist spezialisiert auf umfassende Beratungsleistungen für Banken, Asset Manager, Versicherungsunternehmen und FinTechs. Mit unseren spezialisierten Teams unterstützen wir unsere Kundinnen und Kunden ganzheitlich bei allen strategischen und operativen Herausforderungen von unseren Standorten in Düsseldorf, Frankfurt, Hamburg und München.
Mandatory Tool Skills: Excellent proficiency in MS Project is a must-have. You should be able to create, manage, and analyze complex schedules independently. Desired Tool Skills: Experience with Primavera P6 is highly desirable and will be considered a significant advantage.
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.
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 Bachelor's Degree (BA/BS) in Health Sciences or related field, or equivalent academic/professional qualifications Clinical research experience at the site level required Nurse or other healthcare professional preferred CRA experience preferred High flexibility to travel (including internationally if needed).
Fluent written and verbal communication skills in German language (minimum C1 level), along with a strong command of English.Ability to work independently, manage multiple priorities, and collaborate effectively within cross-functional teams. Willingness to travel within the assigned region (up to 40-60% of working time).
Serves as Data Center technical subject matter expertise and hands on participation to maintain, troubleshoot and manage Data Center Systems. Essential Functions: Manages the installation, maintenance, and upgrades of internal and external computer hardware systems used for designing, developing, and deploying company products.Works with Infrastructure and Business services to provision and setup environments.Assist with designs of automation scripts and best practice processes to minimize the human intervention required for Data Center Environments.Proposes and guides implementation of systems and enhancements that will improve the reliability and performance of the Data Center Environment.Monitors usage and performance and utilizes all standard tool sets for management of all aspects of the Data Center environment.Responds to production issues escalated by client and support teams –requires a deep understanding of the Data Center functionality, architecture, and design, as well as production hardware infrastructure design.Trains personnel on Data Center Processes and systems.Works with Service Providers to ensure that the operational aspects of a Data Center are working properly.
Tasks typically include, but are not limited to: Document management: Set-up and management of clinical document in the Electronic Document Management System (EDMS) Review and approval of the Statistical Analysis Plan in the EDMS Management of timelines including proposal of timelines to trial/project team (based on timelines communicated by sponsor), finalising them after agreement, and updating them as appropriate Preparation for and attendance of the required trial team meetings or submission meetings Preparation, conduct, and documentation of kick-off meetings, e.g. for TDO/CTP, IB or CTR writing Preparation, conduct, and documentation of Results Alignment Meetings (RAM; not applicable for Phase I in healthy volunteer studies) Writing of drafts including appropriate in-text tables and figures according to the timelines agreed upon with trial/project team Provision of drafts and management of all review cycles by the trial/project team, reaching consensus on comments/changes, integration of changes into the text, and completion of the Review Documentation Form (as applicable) Initiation and monitoring or conducting of Quality Control (QC) checks as well as completion of the Quality Control Documentation Form (QCDF) Creation and provision of the final document version to the trial/project team Initiation of publishing and pre-archive checks, monitoring and resolution of findings E-approval of final clinical document in the EDMS Technical checks after the final draft of initial IBs and IB updates in the EDMS, and by going through a Final Formatting checklist document FTE Medical Writer will follow the appropriate process as per document type and according to sponsor SOPs Qualifications Bachelor’s degree in a scientific, clinical, regulatory, or related field required; advanced degree (e.g., MSc, PhD, PharmD, MD) preferred Approx 5 years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be considered Strong knowledge of global regulatory requirements and guidelines (e.g., ICH, FDA, EMA) across all phases of clinical development Broad understanding of clinical research processes, including study design, data analysis, and regulatory submission requirements Demonstrated ability to lead writing activities for complex documents and provide strategic input to cross-functional teams Excellent written and verbal communication skills, with the ability to clearly and accurately present complex scientific and clinical information Strong organizational, time management, and project management skills, with the ability to manage multiple priorities and meet tight deadlines Proven ability to work collaboratively in a cross-functional, team-oriented environment while also operating independently when needed High attention to detail with a commitment to quality, consistency, and scientific accuracy Proficiency in Microsoft Word and document formatting best practices Experience with electronic document management systems (eDMS) and familiarity with document templates, style guides, and structured authoring tools IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
📌 Overview We are seeking an experienced Senior Site Contracts Associate to manage contract strategy and oversee all start‑up contracting activities for selected sponsors. In this role, you will support complex studies and multi‑protocol programs, ensuring high-quality delivery and operational excellence.
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage clinical research projects in different therapeutic areas and to cooperate closely with one of our key clients. The country Clinical Research Lead (CRL) responsibilities include operational delivery of strategic clinical studies assigned to the country, in accordance with ICH/GCP, Incyte SOPs, local operating guidelines and local requirements.
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.
As the world’s largest clinical trial site network and CRA footprint we empower our clinical teams to work confidently collaboratively and globally. Responsibilities: Manage and execute the site identification process and perform regulatory start-up and maintenance activities in accordance with regulations SOPs and project requirements.Prepare and manage site regulatory documentation.Review and negotiate site regulatory documents and contracts with sites and sponsors.Maintain review and report on site performance metrics.Serve as the primary point of contact for investigative sites.Track completion of regulatory and contractual documents for sites.Ensure contracts are fully executed.Establish project timelines.Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations SOPs project requirements and contractual/budgetary guidelines.Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites Site Activation Manager (SAM) Project Management team and other departments as necessary.Ensure adherence to SOPs Work Instructions (WIs) quality of designated deliverables and project timelines.Perform start-up and site activation activities according to applicable regulations SOPs and work instructions.Distribute completed documents to sites and internal project team members.Prepare site regulatory documents reviewing for completeness and accuracy.Ensure accurate completion and maintenance of internal systems databases and tracking tools with project-specific information.Review and provide feedback to management on site performance metrics.Review establish and agree on project planning and project timelines.Ensure monitoring measures are in place and implement contingency plans as needed.Inform team members of completion of regulatory and contractual documents for individual sites.Review track and follow up on the progress approval and execution of documents regulatory ethics Informed Consent Form (ICF) and Investigator Pack (IP) release documents in line with project timelines.Provide local expertise to SAMs and project team during initial and ongoing project timeline planning.Perform quality control of documents provided by sites.May have direct contact with sponsors on specific initiatives.
Lead trial oversight meetings as applicable, communicate status transparently, and secure timely, well-informed decisions from stakeholders and decision-making forums. Manage safety, risk, issues and escalation: Anticipate trial risks, assess impact, define risk-balanced mitigation, track corrective actions and escalate with appropriate timing, context and proposed solutions.
CHEPLAPHARM Arzneimittel GmbH sucht in eine/n Manager Procurement Excellence & Business Process Management (m/w/d) (ID-Nummer: 14532810)
BauWatch Projekt Service GmbH sucht in Frankfurt, Mainz, Wiesbaden, Darmstadt eine/n (Senior) Key Account Manager/in (m/w/d) - Data Center (ID-Nummer: 14529868)
Precitec Optronik GmbH sucht in eine/n Office Manager / Organisation & Unternehmensservice (m/w/d) (ID-Nummer: 14528512)
4C GROUP AG sucht in München, Frankfurt, Berlin, Düsseldorf eine/n Manager Turnaround Manager (w/d/m) (ID-Nummer: 13744044)
EY-Parthenon sucht in eine/n EY-Parthenon Manager Risk & Regulatory - Transaction Diligence (Financial Services) (w/m/d) (ID-Nummer: 14575849)
KG sucht in Darmstadt, Frankfurt am Main, Wiesbaden eine/n Supply Chain Manager (m/w/d) (ID-Nummer: 13503868)
4C GROUP AG sucht in München, Berlin, Frankfurt, Düsseldorf eine/n Manager Controlling (w/d/m) (ID-Nummer: 12937672)
Hilti Deutschland AG sucht in Mannheim, Heidelberg, Frankfurt, Karlsruhe eine/n Sales Manager (m/w/d) - Außendienst für Großkunden in den Regionen Mannheim, Heidelberg, Frankfurt, Karlsruhe (ID-Nummer: 14537171)
Fissler GmbH sucht in eine/n Global Brand Manager (w/m/x) | Fissler GmbH (ID-Nummer: 14146235)
Piepenbrock Unternehmensgruppe GmbH + Co. KG sucht in eine/n Regionaler Sales Manager (m/w/d) (ID-Nummer: 14543190)
Hilti Deutschland AG sucht in eine/n Sales Manager (m/w/d) - Außendienst für Großkunden in den Regionen Mannheim, Heidelberg, Frankfurt, Karlsruhe (ID-Nummer: 14541472)
Stadt Mörfelden-Walldorf sucht in eine/n Abteilungsleitung Zentrale Dienste (w/m/d) (Verwaltungsmanager, Public Manager (w/m/d) o. ä.) (ID-Nummer: 14569329)
Hays – Interne Karriere bei Uns sucht in eine/n Senior Sales Manager (m/w/d) (ID-Nummer: 14563740)
Aerotec Group sucht in eine/n Sales & Business Development Manager – MRO (m/w/d) (ID-Nummer: 14570482)
Bauplanung Stoessel GmbH sucht in eine/n Projekt-Manager/in Immobilien (m/w/d) (ID-Nummer: 14434836)
wenglor sensoric gmbh sucht in eine/n Vertriebsmitarbeiter/Technical Sales Manager (m/w/d) Sensortechnologien im Außendienst im Großraum Frankfurt / Darmstadt / Mannheim / Heilbronn (ID-Nummer: 14281138)
HAPEKO Deutschland GmbH sucht in eine/n Gebietsverkaufsleiter / Area Sales Manager (m/w/d) (ID-Nummer: 14510247)
CHEPLAPHARM Arzneimittel GmbH sucht in eine/n (Senior) CMO Supply Manager (m/w/d) (ID-Nummer: 14592375)
EY Deutschland sucht in eine/n (Senior) Manager Accounting Advisory Banken (Financial Services) (w/m/d) (ID-Nummer: 14575249)
Permodo GmbH sucht in eine/n Customer Success Manager (m/w/d) (ID-Nummer: 14416704)
Nexia GmbH Wirtschaftsprüfungsgesellschaft / Steuerberatungsgesellschaft sucht in Frankfurt am Main, Köln, Mannheim eine/n (Senior) Manager / Wirtschaftsprüfer (m/w/d) in der Qualitätssicherung (ID-Nummer: 14597311)
Für unseren Standort in Frankfurt am Main suchen wir Sie zur Verstärkung unseres Teams als Airfreight Manager (m/w/d) unbefristet in Festanstellung und Vollzeit Jobbeschreibung Als Airfreight Manager sind Sie verantwortlich für die Verwaltung und Steuerung des Erfolges Ihrer Mitarbeiter.
FM-Partner, Instandhaltungsdienstleister, technische Gewerke), bewertest Risiken (Single Source, Kapazitäten, SLA-Erfüllung) und stärkst die Resilienz der Versorgung. Ausschreibungen für Services, Maintenance & CAPEX managen Du bereitest RFIs/RFPs/RFQs für Dienstleistungen, Rahmenverträge und Investitionsbedarfe vor, koordinierst die Angebote mit den Fachbereichen und sorgst für eine strukturierte, vergleichbare Bewertung (inkl.
Lieferantennetzwerk qualifizieren und ausbauen Du baust ein robustes, qualifiziertes Lieferantennetzwerk auf und entwickelst es gemäß pharmazeutischer Qualifizierungs- und Compliance-Anforderungen weiter. Single-Source-Risiken aktiv managen Du identifizierst Abhängigkeiten, steuerst Single-Source-Szenarien und setzt Maßnahmen auf, um Supply-Risiken frühzeitig zu reduzieren.
Lieferantennetzwerk qualifizieren & resilient aufstellen Du baust ein robustes, qualifiziertes Lieferantennetzwerk auf und entwickelst es weiter – inklusive aktivem Single-Source-Management und Bewertung von Supply-Risiken im regulierten Umfeld. Ausschreibungen für Materialien, Packmittel & Services managen Du bereitest RFIs/RFPs/RFQs vor, koordinierst sie mit internen Stakeholdern und bewertest Angebote strukturiert – insbesondere für vial-/fluidrelevante Packmittel sowie externe Partner (z.
Single-Source-Management) und entwickelst es gemäß pharmazeutischer Qualifizierungs- und Compliance-Anforderungen weiter. Ausschreibungen für Materialien & Lohnherstellung managen Du bereitest RFIs/RFPs/RFQs vor, koordinierst sie mit den internen Stakeholdern und bewertest Angebote strukturiert – insbesondere für tablet-/kapselrelevante Materialien und externe Partner (z.
Faltschachteln, Beipackzettel, Etiketten). Ausschreibungen für Packaging managen Du bereitest RFIs/RFPs/RFQs für Packmittel und passende externe Partner (z. B. Druckereien, Konfektionierer, Co-Packer) vor, koordinierst sie mit internen Stakeholdern und bewertest Angebote strukturiert.
Quality Agreements in Abstimmung mit Quality) passend abgebildet sind. Risiken, Kosten und Working Capital managen Du analysierst Beschaffungsmärkte, Trends, Kostentreiber und Supply-Risiken, führst Value-Analysen/TCO-Rechnungen durch und treibst Kostenreduktionsprogramme – bei gleichzeitiger Sicherstellung der Versorgung unter GMP/GDP.
Single-Source-Management und Risikobewertung). Ausschreibungen für Consulting- & Scientific-Services managen Du bereitest RFIs/RFPs/RFQs vor, koordinierst diese mit internen Stakeholdern und bewertest Angebote strukturiert – inklusive Methodik, Deliverables, Zeitplan, Ressourcenprofil, Governance und messbaren Erfolgskriterien.