Want to be part of our team at Women's Healthcare Center? Explore our job openings and see how you can contribute to high-quality women's healthcare. View our open positions now and apply today. What are we looking for? As a Medical Secretary at Women's Healthcare Center, you are the face of our reception desk and work in the secretariat. Where you take on various front and back office tasks. You are responsible for, among other things, receiving patients at the counter, maintaining the agendas and making appointments, and you answer medical questions on the phone. Together with your colleagues, you are responsible for the entire course of affairs surrounding the doctors' consultation hours. Job requirements - Several years of work experience at an outpatient clinic as a medical secretary is an advantage - You can work independently, are stress-resistant and work accurately - Patient focus is central to Women's Healthcare Center and is therefore an important part of the position - It goes without saying that you have good communication and social skills and a very customer-oriented attitude. - You have a good command of the Dutch language, both spoken and written, and can speak English well. - You are also proficient in using email and Windows - Given the diversity of tasks, we expect a collegial attitude and flexible deployment Who are we Women's Healthcare Center is an independent treatment center (ZBC) for women's care with specialists in the field of gynecology, urology and radiology. Women's Healthcare Center aims to treat patients in a calm and friendly atmosphere outside of the hospital atmosphere. The aim is to provide personal guidance which should lead to optimal quality of care provided. We offer We offer you a challenging job in a pleasant, small working environment. This is a temporary position, initially for a period of 1 year. Depending on your experience and education, you will be classified and we offer employm...

What are you looking for? Loading component... Medical Monitoring High quality oversight for safety and compliance. Expert medical monitoring is crucial for streamlining clinical research. An integrated approach will improve outcomes while ensuring trial subject safety. We offer unrivaled expertise in medical monitoring services, providing tailored solutions in accordance with study specifications and requirements. Our safety physicians have extensive knowledge of a broad range of therapeutic areas and will support essential project oversight and procedure clarity, enabling close interaction with key partners and timely delivery of evaluations. We also offer support for smooth patient recruitment, ensuring safety and helping you to define and qualify inclusion/exclusion criteria. Our experts provide high-quality medical review services for study protocols, clinical study reports, review and approval of MedDRA and ATC codes, as well as medical reviews of a wide range of safety data, including adverse effects (AEs) and serious adverse effects (SAEs) reported in the clinical and/or safety database. Additional services include independent medical monitoring for safety review meetings and participation in Independent Data Monitoring Committees (IDMCs) and Data Safety Monitoring Boards (DSMBs). SGS is recognized as the benchmark for quality and integrity in clinical research. We are your first choice when looking for exceptional customized medical monitoring for your research project.

Medical Advisor - Location: Amsterdam, Netherlands - Contact: Stefan Charles - Job type: - Contact phone: +31 (0)20 406 97 50 - Industry: Clinical Research - Contact email: stefan_charles@oxfordcorp.com Our client operates within the global pharmaceutical industry and focuses on clinical research and the development of innovative therapies. Working in a highly regulated and collaborative environment, the organization supports clinical studies that contribute to advancing healthcare. To strengthen the Clinical Study team, our client is seeking a Medical Advisor who can bridge science, operations, and stakeholders. Job Description As a Medical Advisor, you act as the medical and scientific expert within clinical trial activities. You support both local and international study teams by ensuring that research is conducted in line with regulatory standards and scientific best practices. The role involves advising on study designs, supporting feasibility assessments, and addressing medical questions that arise during trials. You collaborate with internal departments and external partners such as investigators and specialists, ensuring strong alignment between global strategies and local execution. You also contribute to documentation and support communication with regulatory authorities. Requirements - Medical degree preferred, or PhD/PharmD in life sciences. - Strong scientific knowledge and understanding of clinical development. - Experience in clinical practice, research, or pharmaceutical development. - Familiarity with ICH-GCP guidelines and regulatory frameworks. - Strong stakeholder management and communication skills. - Fluent in English. - Proactive, independent, and comfortable working in a dynamic environment. - Work visa required, and already situated in the Netherlands. If these requirements are not met you will not receive a response to your application

Head of Medical Safety GCSP At Bavarian Nordic, we are committed to saving and improving lives by unlocking the power of the immune system. Our commercial portfolio includes market\-leading vaccines against smallpox/mpox, rabies, tick\-borne encephalitis, typhoid fever, and cholera. We excel in R\&D innovation, manufacturing, and commercialization\-working every day to protect people's health and quality of life and protecting our tomorrow. We are looking for an experienced Head of Medical Safety GCSP providing medical leadership across Global Clinical Safety \& Pharmacovigilance (GCSP). The position reports to the Head GCSP \& EU/UK QPPV and can be based in either Germany or Switzerland \- travel up to \~20% within Europe should be expected. The roleAs our Head of Medical Safety GCSP, you will be accountable for all medical safety related aspects of clinical safety and pharmacovigilance as well as ad hoc safety issues and innovation projects in your area of expertise. In this role, you will manage and mentor a team of six (Sr) Safety Physicians and (Sr) Safety Scientists. Key responsibilities Lead and develop the medical safety team and ensure that appropriate tools and skillsets are available/developed Ensure high quality clinical safety contributions to development programs and for the life\-cycle management of marketed products in compliance with regulations, guidelines, BN operating procedures (SOPs) Serve as member of the GCSP Leadership Team and in governance committees as assigned Ensure medical safety support for GCP and GVP audits and inspections Contribute to company strategic initiatives and innovations Stay abreast of innovative technologies, tools, innovations, and regulations concerning area of expertise What you bringTo become a success in this role, you bring a Medical Doctor (MD) degree combined with leadership experience within clinical safety and pharmacovigilance. You are recognized for setting direction, taking accountability, and leading teams with passion, clarity and empathy in a highly regulated, global environment. You balance strategic oversight with confident decision?making and strong ethical stakeholder engagement. 10\+ years of experience across clinical safety and pharmacovigilance, including senior Medical Safety roles Deep regulatory expertise across global safety activities, including signal management and risk minimization You bring solid knowledge of global clinical safety and pharmacovigilance regulations including GCP, GVP, and ICH guidelines, along with hands\-on experience in CTD compilation and MAAs/BLAs submissions to major health authorities. Besides this, you communicate fluently in English with solid written, verbal, and presentation skills using medical and regulatory terminology. You are highly proficient in relevant IT tools and database applications and are a self\-driven, positive team player who helps to build and sustain high performance and team cohesion. Most importantly, you thrive in change; your judgment, integrity, and resilience help safeguard patient safety and support our transition from development to full commercialization in a fast\-moving, life\-science environment. Please note an advanced degree is required, and an MD qualification is mandatory for this role. Why this roleThis role offers a unique opportunity to take end?to?end responsibility for all medical safety activities within clinical safety and pharmacovigilance in a science driven organization with a strong purpose. You will mentor a team, work closely with global stakeholders, contribute directly to regulatory submissions and patient safety, and have real influence on how safety processes and risk management activities are shaped and executed. It is a role with both strategic impact and hands?on responsibility, ideal, if you want to grow your expertise while making a meaningful difference. In this role, you will have the platform to make a lasting impact on public health, advance our mission, and set new benchmarks for medical excellence in a dynamic, growth\-oriented biotechnology environment. ApplicationIf you are ready to take on a pivotal role in a growing organization and drive meaningful change in healthcare, apply now and join Bavarian Nordic in our mission to improve health outcomes and foster sustainable growth. Please note that we do not support any relocation package for this role. We kindly request that headhunters or recruitment agencies refrain from contacting us regarding this position. Bavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America. Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For more information, visit jpid589a182jm jit0623jm jiy26jm

Global Medical Marketing Manager We are looking for someone to start immediately or by agreement: Global Medical Marketing Manager m/w/d (100%) As a Swiss family business with a 160\-year history, we at SIGVARIS GROUP employ more than 1,600 people worldwide. We are committed to helping people feel good every day with high\-quality and innovative products in the field of medical compression therapy. Our portfolio covers a wide range of needs and indications. Continuous development and innovation, as well as a consistent commitment to solutions that support our customers in all their activities, make us the preferred partner for all stakeholders. At SIGVARIS GROUP, we are committed to creating an excellent working environment for our most valuable asset: our employees. Their talents, diversity and commitment are crucial to our innovative strength and success. Your responsibilities: Define and lead the global medical activation plan across "MOH", congresses, KOL initiatives, and educational campaigns Own the global MOH roadmap, content planning process, and activation calendar in collaboration with the agency and internal stakeholders Lead the planning and execution of global congresses, medical symposia, speaker programs, and advisory board support Coordinate external medical communication and scientific storytelling in alignment with global medical priorities Ensure scientific narratives are translated into engaging and compliant activation formats for HCPs and stakeholders Manage and guide the MOH / medical marketing agency across content, channels, events, operations, and reporting Work closely and co\-manage with other medical team members, the global and regional scientific societies and associations to build long term win\-win partnerships Collaborate with the Clinical Evidence Manager to ensure scientific robustness of external content and event topics Collaborate with the Medical Training Manager to ensure educational consistency and high learning value across MOH and congress activities Build and maintain KOL engagement plans related to medical activation, congress participation, and educational formats Create and maintain a global advisory board to our focus indications Coordinate closely with Global Product Management, Branding, Innovation and Regions to ensure alignment and local relevance Support regional adaptation and adoption of MOH and medical communication initiatives Monitor performance and engagement metrics across digital medical activation and recommend optimization actions Your qualifications: Degree in Life Sciences, Healthcare Marketing, Medical Communication, or related field 5\+ years of experience in medical marketing, scientific communication, congress management, or HCP engagement Experience in Phlebology and/or Lymphology is a big plus Attending regular weekly meeting in St. Gallen office Strong experience in digital medical education, congresses, and agency management Ability to translate scientific content into compelling external activation Strong project management, stakeholder alignment, and execution capabilities Experience working cross\-functionally with Medical, PM, Branding, and Regions Fluent in English and German, other languages especially French highly valued Willingness to travel for congresses, key events, and stakeholder meetings 30\-40% travel time required. What we offer: Be part of an international company and contribute to people's well\-being with a variety of tasks. Every day Work independently with plenty of room for personal and professional development Stable family business with a strong market and value orientation Competitive salary \& benefits as well as excellent insurance coverage Flexible working model, including the option to work from home Are you interested in this exciting role? If so, please send us your application. Apply now SIGVARIS AG \- Gröblistrasse 8 \- 9014 St. Gallen jid8c937efjm jit0521jm jiy26jm

Associate Director, Medical Affairs Obesity Medical & Scientific Affairs, International Operations Strategic Office Zurich, Switzerland If you’re driven by a desire to translate cutting-edge science into real-world clinical impact, elevate standards of care, thrive through collaboration, and help reshape how the world understands obesity—this is your moment. At Novo Nordisk we are looking for an Associate Director, Medical Affairs – Obesity, to help lead the evolution of one of the most transformative therapy areas in modern medicine—and one of the greatest healthcare challenges of our time. Your New Role As Associate Director, Medical Affairs – Obesity, you’ll play a pivotal role in advancing Novo Nordisk’s global obesity strategy across International Operations (IO)—covering all markets outside the U.S. You’ll operate at the scientific forefront, turning the latest research into meaningful medical advances, while ensuring our approach to obesity and related conditions is rooted in evidence, empathy, and excellence. You’ll serve as a trusted scientific partner across regions and functions—shaping how we engage with healthcare professionals, key opinion leaders, and patients. Your work will directly influence how obesity is understood, treated, and prioritized in more than 190 countries. Your key responsibilities will be: Lead the execution of medical strategy and tactics for obesity and related conditions across IO, incl. new product launches ensuring tight alignment with global medical and development priorities. Champion obesity as a serious, chronic disease, while integrating insights across the broader cardiometabolic portfolio. Partner with regional and affiliate Medical Affairs teams to strengthen medical education, scientific exchange, and patient journey insights. Represent market and regional perspectives in global forums—to shape clinical development and communication strategies. Drive high-impact scientific engagement with thought leaders, academic institutions, and professional societies to elevate the global narrative around obesity. You will also support RWE and data generation initiatives in collaboration with global and local teams, aligning with medical and access goals. Operate effectively in a global, matrixed environment, partnering across Medical, Clinical, Commercial, and Access functions. This is a role for someone who brings both intellectual rigor and relentless dedication—someone ready to go the extra mile to deliver strong results and make a lasting difference, all within a supportive, values-driven environment that champions sustain-able high performance. Please note: For Zurich-based roles at this level within IO Strategic Operations, international mobility within a three-five year horizon is expected. Your New Team You’ll join the IO Cardiometabolic Medical & Scientific Affairs team—a dynamic, mission-driven group at the heart of Novo Nordisk’s fastest-growing therapeutic area. Reporting to the Director, Medical Affairs Obesity, you’ll be part of a global network of medical leaders shaping the future of care for people living with obesity and related conditions. Based in Zurich, Switzerland, you’ll work from our International Operations Strategic Office—a hub for innovation, talent development, and cross-regional collaboration. As part of Novo Nordisk’s Talent Incubator, this role offers exceptional exposure to global strategy and the chance to build an international network that can accelerate your career. Your Skills & Qualifications We’re looking for a scientifically rigorous, strategically agile, and highly collaborative leader who thrives where medicine, science, and business impact intersect. What you bring: MD preferred, or an advanced scientific degree with 7+ years of experience in the pharmaceutical industry – ideally, though not mandatorily, in obesity, endocrinology, or cardiometabolic diseases. Proven track record in Medical Affairs, including experience in pre-launch planning, scientific communication, and stakeholder engagement. Solid understanding of clinical development pathways, regulatory frameworks (EMA/FDA), and real-world evidence generation. Demonstrated ability to lead cross-functional initiatives and influence without formal authority in a global matrix. Exceptional scientific communication, analytical thinking, and presentation skills—with the ability to distill complex data into clear, compelling narratives. A proactive, solutions-oriented mindset and deep commitment to improving outcomes for people living with obesity. Above all, you combine scientific depth with strategic execution, and you believe—wholeheartedly—that obesity deserves the same seriousness, investment, and innovation as any other chronic disease. Working at Novo Nordisk At Novo Nordisk, we don’t just treat diseases—we redefine what’s possible. For over a century, our “unordinary” mindset has driven us to challenge conventions, champion patients, and pursue science with purpose. We know careers aren’t linear—and lives aren’t one-size-fits-all. That’s why we foster a culture of mutual respect, curiosity, and sustainable high performance, where your growth matters as much as our mission. Here, dedication is valued. You’ll be part of a global community united by a simple truth: Together, we’re life-changing. What We Offer Beyond a competitive compensation package, we offer continuous learning, global mobility opportunities, and a people-first culture. Our benefits are thoughtfully designed to support both your professional ambitions and personal well-being—at every stage of your journey. Ready to Make an Impact? If you’re ready to lead with science, collaborate with purpose, and help transform the future of obesity care, we’d love to hear from you. To submit your application, please upload your CV in English (click on Apply and follow the instructions).

FMTC logo Amsterdam - Instructor Medical Frist Aid & Medical Care - On-site - - Amsterdam , Noord-Holland , Netherlands - • Schiphol , Noord-Holland , Netherlands • +1 more Job description Do you thrive on inspiring others, sharing knowledge, and making a real impact through hands-on training? Are you someone who takes ownership, embraces variety, and feels at home in an international and fast-moving environment? For our training center in Amsterdam , we are looking for a driven and passionate Medical First Aid & Medical Care Instructor (m/f/d) who wants to enable people to work safely and optimally prepare them for emergency situations in offshore environments. Who Are We? At FMTC Safety, everything revolves around people and safety. We are a fast-growing, global organization preparing professionals to work safely in some of the world's most demanding environments: from offshore platforms and wind farms to ships and industrial sites. What makes us different? We go where our clients need us. With training centers strategically located around the world, we offer maximum flexibility: in timing, location, and delivery. Our mindset is simple: we make it happen . Even if there's only one participant, the training goes ahead. This requires more than just knowledge, it requires passion, flexibility and a true customer-first mentality. And that's exactly what defines our instructors. Job requirements Your Role as a Medical First Aid & Medical Care As a Medical First Aid & Medical Care Instructor (m/f/d) in Amsterdam , you are at the heart of our training center. You don't just deliver courses, you create impactful learning experiences that truly prepare people for real-life offshore emergencies. What will you do? No two days are the same and that's exactly what excites you. You take full ownership of your trainings and: - Deliver Medical First Aid and Medical Care courses - Guide practical exercises, such as life-saving a...

L'institut de Cancérologie de Bourgogne est dirigé par des oncologues-radiothérapeutes et des oncologues médicaux associés. Le fonctionnement des 3 sites est assuré par : - Des médecins, oncologue médicaux et radiothérapeutes dirigeants - Une directrice générale et une équipe administrative assurant des fonctions transversales - Des manipulateurs d'électroradiologie - Des secrétaires médicales - Des dosimétristes, - Des physiciens médicaux Les trois centres disposent d'un service de radiothérapie et le centre de Dijon dispose également d'une structure de consultations en chimiothérapie, et de traitement en curiethérapie. Le poste recherché est basé à Chalon sur Saône, pour un CDI et à temps plein Le/la secrétaire médical(e) est l'interlocuteur(trice) privilégié(e) des médecins, de l'équipe soignante, des patients, des services extérieurs au centre. Il/Elle a pour missions générales : d'accueillir les patients, de les aider dans leur démarches, d'organiser le planning des médecins, de prendre en charge les appels téléphoniques, le courrier, de constituer les dossiers médicaux et de gérer les hospitalisations. Le/la future secrétaire médical(e) aura en charge : - Accueil des patients - Accueil téléphonique. - Frappe des courriers. - Classement des courriers entrants et des fax. - Affranchissement et envoi des courriers - Gestion des rendez-vous internes et externes. - Préparation du dossier médical pour les consultations et création du dossier administratif informatique et archivage des dossiers - Gestion des transports des patients - Gestion de la facturation des consultations, des traitements et gestion du règlement des consultations Missions spécifiques : -Gestion de la facturation des consultations et des traitements -Gestion du règlement des consultations Une formation sera assurée sur place par l'équipe actuelle de secrétaires. L'équipe est composée de 5 secrétaires et d'une secrétaire responsable Profil : Formation SECRETAIRE MEDICAL(E) et EXPERIENCE SECRETARIAT MEDICAL(E) NECESSAIRE

Für die Medizinische Hochschule Brandenburg Theodor Fontane wird zum 1. Januar 2027 eine/ein Präsidentin/Wissenschaftliche Geschäftsführerin bzw. Präsident/Wissenschaftlicher Geschäftsführer (m/w/d) gesucht. Die Medizinische Hochschule Brandenburg Theodor Fontane (MHB) ist eine staatlich anerkannte Hochschule in kommunaler und gemeinnütziger Trägerschaft. Sie steht für innovative Lehr- und Forschungskonzepte sowie für die Einheit von Forschung, Lehre und Patientenversorgung. Mit den MHB Hochschulstandorten und Universitätskliniken Bernau, Rüdersdorf, Neuruppin und Brandenburg an der Havel sowie aktuell landesweit mehr als 31 kooperierenden Kliniken und rund 350 Lehrpraxen sieht sie ihren Gründungsauftrag in einer Antwort auf geänderte Anforderungen an das Gesundheitswesen im Land Brandenburg und in vergleichbaren Regionen. Dementsprechend widmet sich die MHB schwerpunktmäßig dem Thema Gesundheit und Krankheit des Alterns. Die/Der Präsidentin ist gleichzeitig Wissenschaftlicher Geschäftsführer*in der MHB. Für die verantwortungsvolle Aufgabe als Präsidentin/Präsident und Wissenschaftliche Geschäftsführerin/Wissenschaftlicher Geschäftsführer suchen wir eine gestalterische Führungspersönlichkeit mit Überzeugungskraft, Motivationsvermögen sowie Kommunikations- und Kooperationsfähigkeit. Sie/Er soll die innovativen Ansätze der Universität weiterentwickeln und die Vernetzung der Universität mit der Region, den universitären und nicht-universitären Forschungseinrichtungen des Landes und der Politik weiter erfolgreich vorantreiben. Sie sind eine herausragende und engagierte Führungspersönlichkeit, die über folgendes Profil verfügt: ausgewiesene Erfahrung und Kompetenz im Management und in der Strategieentwicklung langjährige Leitungserfahrung in einer Stellung mit herausgehobener Verantwortung in Wissenschaft und/oder Wirtschaft nachgewiesene Kompetenzen in der Forschung und Lehre, in einer aufstrebenden wissenschaftsbasierten Einrichtung profunde Kenntnisse der nationalen und internationalen Hochschullandschaft Erfahrungen im Umgang und in Kooperationen mit Akteuren in herausgehobener Verantwortung aus Wissenschaft, Gesellschaft, Politik und Wirtschaft ein Interesse und Erfahrung in der digitalen Medizin und medizinnahen Tätigkeit eine Habilitation oder Professur Die Berufung/Wahl erfolgt für 5 Jahre, Wiederwahlen sind möglich. Die Präsidentin/Der Präsident wird entsprechend §13 (3) Grundordnung der MHB aufgrund des Wahlvorschlags einer gemeinsamen Findungskommission von Senat und Gesellschaftern vom Senat gewählt und von der Gesellschafterversammlung der Trägerin nach Maßgabe des Gesellschaftsvertrages zur Geschäftsführerin/zum Geschäftsführer der Trägerin bestellt. Die Medizinische Hochschule Brandenburg strebt eine Erhöhung des Anteils von Frauen im wissenschaftlichen Bereich an und lädt Frauen nachdrücklich zur Bewerbung ein. Bei gleicher Eignung werden schwerbehinderte Bewerber*innen bevorzugt berücksichtigt.

An der Medizinischen Hochschule Brandenburg Theodor Fontane (MHB) ist zum nächstmöglichen Zeitpunkt eine Vollzeitstelle (40 Stunden pro Woche, Teilzeit möglich) als Ärztlich-Wissenschaftlicher Mitarbeiterin als Lehrkoordinator*in (m/w/d) am Institut für Allgemeinmedizin am Standort Brandenburg an der Havel zu besetzen. Die Stelle umfasst die (Weiter-)Entwicklung, Koordination, Durchführung und Sicherstellung qualitativ hochwertiger Lehrveranstaltungen in der Allgemeinmedizin. Die Stelle ist auf 24 Monate befristet, mit der Option zur Verlängerung. Das Institut für Allgemeinmedizin der MHB setzt sich für die hausärztliche Ausbildung und Forschung in Brandenburg ein. In enger Zusammenarbeit mit den Lehrpraxen vor Ort werden den Studierenden der MHB praxisnahe Fertigkeiten, ein fundiertes Verständnis und vor allem Begeisterung für die hausärztliche Tätigkeit vermittelt - bereits ab dem ersten Studienabschnitt. In Kooperation mit dem Forschungspraxen-Netzwerk der MHB lassen sich praxisrelevante Fragestellungen wissenschaftlich untersuchen und neue Erkenntnisse direkt in der klinischen Versorgung erproben. Vor diesem Hintergrund übernehmen Sie eine zentrale Rolle in der Umsetzung und (Weiter-)Entwicklung der Lehraktivitäten des Instituts, gern auch in Verbindung mit einer parallelen klinischen Tätigkeit: Entwicklung, Planung und Durchführung hochqualitativer Lehrveranstaltungen und Prüfungen in der Allgemeinmedizin Fachlich fundierte Betreuung und Qualifizierung von Lehrpraxen mit regelmäßigen Vor-Ort-Besuchen zur Sicherstellung hoher Ausbildungsstandards Akquise, Auswahl und Koordination externer Lehrender zur nachhaltigen Sicherung eines exzellenten Lehrangebots Mitwirkung an der Weiterentwicklung des Curriculums sowie Planung und Umsetzung innovativer Lehrprojekte bei Bedarf Konzeption, Durchführung und fundierte Auswertung von Lehr- und Kursevaluationen zur kontinuierlichen Qualitätssicherung Unterstützung bei wissenschaftlichen Forschungsvorhaben und Publikationen Fachliche Qualifikation: Abgeschlossenes Medizinstudium Fachärzt*in für Allgemeinmedizin oder fortgeschrittene Weiterbildung in der Allgemeinmedizin Fundiertes Wissen in Primärversorgung, Praxisorganisation und Patientenmanagement Erfahrung in Forschung und wissenschaftlicher Publikation von Vorteil Lehre & Didaktik: Nachweisbare Lehrerfahrung und idealerweise medizin-didaktische Qualifikation Freude an der Vermittlung von Wissen und der Arbeit mit Studierenden Erfahrung in der Entwicklung von Lehrformaten und Curricula von Vorteil Fähigkeit, praxisnahe Inhalte anschaulich und motivierend zu vermitteln Arbeitsweise & Persönlichkeit: Selbstständige, strukturierte und effiziente Arbeitsweise Teamorientiert, kommunikativ und organisationsstark Freundliches, souveränes Auftreten Hohe Motivation, die Primärversorgung im Land Brandenburg aktiv zu stärken Interesse an einer akademischen Karriere neben bzw. zusätzlich zur Praxistätigkeit Integrität, Verlässlichkeit und Diskretion in allen Aufgabenbereichen IT-Kompetenzen: Erfahrung mit digitalen Lehrformaten und eLearning-Tools von Vorteil Schnelle Auffassungsgabe für neue Anwendungen Sicherer Umgang mit modernen digitalen Arbeitsmitteln Sprachkenntnisse: Deutsch: sehr gute Kenntnisse in Wort und Schrift (C1/C2) Englisch: gute Kenntnisse in Wort und Schrift (C1) Gezielte Förderung Ihrer akademischen Entwicklung durch Unterstützung bei Promotion, Habilitation und fachbezogenen Fortbildungsmaßnahmen Anrechnung von bis zu 6 Monaten auf Ihre Weiterbildung in der Allgemeinmedizin (in Beantragung) Für nachhaltige Mobilität: vergünstigtes Deutschlandticket als Jobticket; BusinessBike (bei Festanstellung) Attraktive Vergütung gemäß den Richtlinien für wissenschaftliche Mitarbeitende Option auf mobiles Arbeiten Selbstbestimmtes und flexibles Arbeiten (orientiert an unserer Kernarbeitszeit) in einer wertschätzenden Arbeitsatmosphäre 28 Tage Erholungsurlaub (Erhöhung nach Betrieb... Homeoffice: Umfang: Nach Vereinbarung