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.
Qualifications Bachelor's Degree Related field OR 5-year relevant sponsor or clinical research organization clinical site contracting experienceGood negotiating and communication skills with ability to challenge.Strong legal, financial and/or technical writing skills.Strong understanding of regulated clinical trial environment and knowledge of drug development process.Good understanding of clinical trial contract management.Fluent in English and German language IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Ihre Aufgaben Unterstützung der PCMs in der täglichen Arbeit, auch im internationalen Umfeld Unterlagen für jährliche Konformitätsbewertung vorbereiten Vorbereitung und Recherche für Risk-Assessment Zusammenstellung und Pflege von produktspezifischen Technical Files Verantwortliche Zusammenstellung von produktspezifischen Summarized Technical Documentation (STED) Unterlagen für die internationale Registrierung Verantwortliche Zusammenstellung von produkt-spezifischen Unterlagen für die Klinische Bewertung (CER = Clinical Evaluation Report) Ihr Profil Erfolgreich abgeschlossenes wirtschaftliches oder technisches Studium, Technikerausbildung oder Technischer Betriebswirt Berufserfahrung in dem oben aufgeführten Aufgabenbereich Grundkenntnisse im regulatorischen Umfeld von Medizinprodukten hilfreich Sehr gutes Organisationstalent und Flexibilität Selbständige, strukturierte sowie verantwortungsbewusste Arbeitsweise Hohe Leistungsbereitschaft sowie Bereitschaft zur flexiblen Gestaltung der Arbeitszeit Grundkenntnisse im regulatorischen Umfeld von Medizinprodukten hilfreich Sehr gute Englisch-Kenntnisse in Wort und Schrift Das klingt nach einer spannenden Aufgabe für Sie?
Job Overview: As a Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external clients’ needs, across complex projects and studies.
. --------------------------------------------- Senior Data Scientist Data Science & Advanced Analytics Frankfurt, Germany The Senior Data Scientist is responsible for designing, deploying and continuously optimizing scalable ML solutions that translate business requirements into measurable impact across EMEA markets. The position combines technical execution with business alignment, ensuring solutions remain adaptable to evolving commercial needs while maintaining architecture consistency and standardization.