. • Betreuung und Überwachung der Produktionsprozesse (Übersetzung, Layout, Druck) • Steuerung, Monitoring, Reporting und Optimierung von Performance Massnahmen • Kontinuierliche Markt-, Wettbewerbs- und Trendbeobachtungen • Operative Schnittstelle zwischen Produktmanagement, Marketing, Vertrieb , Global Marketing Communication und Headquarters • Sicherstellung der Markenrichtlinien in allen Aspekten der Marketingkommunikation Ihr Profil: • Erfolgreich abgeschlossenes Studium im Bereich Marketing, Digitale Medien, Marketingkommunikation oder eine vergleichbare Qualifikation • mind. 2 Jahre Berufserfahrung im Online-Marketing, hohe Affinität zu digitalem Marketing • idealerweise Erfahrung im B2B Marketing, vorzugsweise in der med-tech Branche • Erfahrung im Website-Management, SEO, Paid Advertising sowie KI-Anwendungen • Erfahrung mit Marketing-Automation-Tools (SAP Marketing), digitalen Analyseplattformen und weiteren relevanten Tools • Kenntnisse im Social Media Marketing • Sicherer Umgang mit Website-Analyse- und Trackingtools wie Google Analytics 4, Google Search Console und Google Tag Manager • Gutes Fachwissen & Begeisterung für aktuelle digitale Trends und technologische Innovationen • Kenntnisse im Umgang mit Adobe Experience Manager, Adobe Indesign und Adobe Photoshop Kenntnisse sowie sehr gute Kenntnisse in MS Office • Sehr gutes sprachliches und textuelles Ausdrucksvermögen in Deutsch • Deutsch fließend in Wort und Schrift und gutes Englisch • Organisationstalent, Sie behalten auch in hektischen Momenten einen kühlen Kopf und die Übersicht • Durchsetzungsfähigkeit und Sicherheit in internationalen und multifunktionalen Teams mit ausgeprägter Teamfähigkeit • hohe Fähigkeit zur Selbstorganisation, Flexibilität und Proaktivität • Präsentationssicherheit und Kommunikationsstärke • Eigeninitiative und große Begeisterungsfähigkeit • Unternehmerisches Denken mit einem Fokus auf Lösungsfindung und abteilungsübergreifender Zusammenarbeit • Hohe kunden- und erfolgsorientierte Arbeitsweise • Hohes Engagement und Selbstständigkeit sowie die Fähigkeit, in einem dynamischen und sich schnell verändernden Marktumfeld erfolgreich zu agieren Was wir Ihnen bieten… • Vielfältige attraktive Sozialleistungen • Eine Altersvorsorge die mitwächst • Ein engagiertes Team und tolle Kollegen • Regelmäßige fachliche und persönliche Weiterbildungsangebote • Flache Hierarchien • Moderner Arbeitsplatz in einem spannenden, dynamischen Umfeld • Betriebliches Gesundheitsmanagement und vieles mehr Haben wir Ihr Interesse geweckt?
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 the health care field.Minimum of two-four years of on-site monitoring experience alternatively an equivalent combination of education, training and experience.Knowledge 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.Fluency in German on at least C1 level and a good command of English.Flexibility to travel up to 40-60% of working time.Driver’s license class B.
Zu Ihren Aufgaben gehören insbesondere: Wissenschaftliche und karrierebezogene Betreuung und Mentoring der Promovierenden Gemeinsame Weiterentwicklung der Forschungsagenda der Gruppe Publikation und Präsentation Ihrer Forschung in internationalen Fachzeitschriften und auf Konferenzen Initiierung und Koordination von drittmittelgeförderten Forschungsprojekten Mitwirkung an institutsweiten Entscheidungsprozessen im gemeinsamen Austausch innerhalb des IMES-Leitungsteams Lehre im neuen Bachelorstudiengang Biomedizintechnik, einschließlich der Konzeption neuer Lehrveranstaltungen Ihr Profil Voraussetzung für die Einstellung ist ein abgeschlossenes wissenschaftliches Hochschulstudium in einem relevanten ingenieurwissenschaftlichen Fachgebiet (z.
Requirements: BSc or MSc degree in Biostatistics or related field and 10+ years’ relevant experience within the life-science industry, along with at least 2 years’ experience in managing staff Familiarity with complex statistical methods that apply to Phase I-IV clinical trials In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Familiarity with moderately complex statistical methods that apply to applicable clinical trials Strong working knowledge of SAS Working knowledge of relevant Data Standards (such as CDISC/ADaM) From camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.
Excellent knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Fluent languages skills in German on at least C1 level and good command of English.
What you should bring: Bachelor’s or higher-level University Degree preferably in life science, or High School Diploma and apprenticeship within the life science, medical or pharmaceutical field or within office management.At least 2-4 years’ experience as Clinical Trial Coordinator or within another administrative role in clinical research, e.g. as Clinical Trials Assistant, Study Start-Up Assistant.Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Fluent languages skills in German on at least C1 level and good command of English.Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.Effective communication, organizational and planning skills.Ability to work independently and to effectively prioritize tasks while working on multiple projects.Ability to establish and maintain effective working relationships with coworkers, managers and clients.Home-office within the following region: Ulm, Neu-Ulm, Memmingen, Ehingen an der Donau, Ravensburg, Leutkirch im Allgäu, etc. and the ability to visit our client’s office on a regular basis.Preferably to start on 1. or 16.
Key Responsibilities: Leadership: Serve as a biostatistical consultant for other members of the department and staff members from other Biostatistics departments within the company Represent sponsors at meetings with regulatory agencies or other regulatory meetings, may participate as a member of a Data and Safety Monitoring Committee Participate in independent research activities, teaching opportunities, presentations, and preparation of manuscripts for publication Participate as high level lead biostatistician on major projects, including developing/reviewing protocols, preparing analysis plans, and writing sections of joint clinical/statistical reports, integrated summaries and/or NDA sections Leading studies at an operational level Provide expert review and initiate methodology development work with regards to statistical standards and validation procedures Consult on operational/statistical/therapeutic area topics Knowledge Sharing: Maintain knowledge and awareness of developments in biostatistics and clinical trial methodology, and regulatory requirements that impact on analyses Performs as subject matter expert (SME) Risk Management: Identifies risks to project delivery and/or quality, leads in a way to minimize risks Anticipates risks to avert need for study level escalations, supports lead in implementing risk mitigation actions Lock and Unblinding Process: Leads the database lock and unblinding process for the statistical team Participate on the biostatistics randomization team (drafts randomization specifications and/or perform quality control (QC) review of randomization schedules) Statistical Expertise: Provide expert statistical input into review of statistical deliverables (i.e. statistical section of a protocol, statistical analysis plans, table shells, programming and table specifications, data review, tables, listings, figures, and statistical sections for complex and/or integrated reports) Provide expert input into data management deliverables (i.e. database design, CRF design, validation checks and critical data) Provide expert review of ADaM reviewers guide (ADRG) and metadata Perform senior biostatistical review (SBR) Produce or perform quality control review of sample size calculations for complex studies Requirements: Masters or PhD degree in Biostatistics or a related field with relevant experience within the life-science industry Expert in a broad range of complex statistical methods that apply to Phase 2-3 clinical trials Expert in strategically collaborating with clinical and drug development expertsExperience in serving as statistical lead for regulatory submissions, including preparation of submission datasets, eCTD support, meeting with regulatory teams, and responding to regulatory queries In-depth knowledge of applicable clinical research regulatory requirements, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Strong working knowledge of SAS or RExcellent knowledge of CDISC Data Standards Superb communication and collaboration skills Independent and pro-active problem solving skills IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Structured and Results-Oriented Mindset Structured, independent and results-driven way of thinking and working with a strong sense of ownership. International and Intercultural Competence High level of intercultural competence with experience working with international teams and diverse stakeholders.
RSV‑spezifische Expertise (wünschenswert) Verständnis von Impfstoff‑Wirksamkeitsendpunkten und Sicherheitsprofilen. Vertrautheit mit nationalen Impfempfehlungen (STIKO) und internationalen Leitlinien. Kommunikationsstarke Persönlichkeit mit ausgeprägter Fähigkeit, komplexe Inhalte verständlich aufzubereiten. Präsentationsstark – sowohl vor klinischen Entscheidungsträgern als auch wissenschaftlichem Fachpublikum.
What sets you apart: Academic & Professional Background Degree in Business, Economics, or Finance with 6–9 years of experience in top-tier strategy consulting (MBB/Tier 2) focusing on operations or value optimization. Proven track record in international healthcare, life sciences, or related industries. Financial & Analytical Expertise Strong analytical skills with deep expertise in P&L drivers and margin-focused initiatives.
Regulatory Strategy & Execution Excellence Proven experience in the development, coordination and leadership of national and international regulatory strategies. Stakeholder & Interface Management High level of competence in managing complex interfaces and engaging with internal and external stakeholders.
In this pivotal role, you will: Lead international media relations to position CSL as a trusted leader in biopharma, plasma economics and healthcare innovation across key international markets.
·Strong global knowledge and awareness/understanding of the biopharma industry, drug development lifecycle and operational clinical trial delivery.In-depth knowledge of applicable clinical research regulatory requirements; e.g. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Strong business acumen including confidence with financial considerations, excellent negotiation and influencing skills, and comfort working in both sales and operational environments.Strong customer management skills and demonstrated ability to understand customer needs, have difficult conversations with internal/external stakeholders and customers, negotiate solutions and understand impacts on the overall program/portfolio.Strong leadership skills, ability to lead a virtual team in a matrix organization.Ability to work strategically to realize organizational and project goals, identifying and developing positive and compelling visions for the successful delivery of projects and taking account of a wide range of issues across, and related to, the projects and the organization.Strong presentation skills.Excellent written, verbal communication and interpersonal skills, including good command of English language (both written and spoken).Strong software and computer skills, including MS Office applications.Must have prior experience in the Clinical Research Organization (CRO) industry MINIMUM REQUIRED EDUCATION AND EXPERIENCE Bachelor's degree in life sciences and relevant global clinical research experience (director level), including hands on operational delivery and/or drug development experience in the applicable therapeutic area (Internal Medicine/Immunology) At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world.
Strategic and Analytical Mindset Excellent analytical and problem-solving capabilities combined with a strategic, results-oriented approach. International and Intercultural Competence Strong intercultural skills with experience working in cross-functional and international teams.
Strategic and Analytical Mindset Excellent analytical and problem-solving capabilities combined with a strategic, results-oriented approach. International and Intercultural Competence Strong intercultural skills with experience working in cross-functional and international teams.
Strategic and Analytical Mindset Excellent analytical and problem-solving capabilities combined with a strategic, results-oriented approach. International and Intercultural Competence Strong intercultural skills with experience working in cross-functional and international teams.
Travel Requirements Position will involve national and occasional international travel, up to 75% of the time, with overnight stays. Languages German English Working Conditions Remote working, with regular internal meetings at national and regional offices depending on business requirements.