En tant que secrétaire médico-social, vous partagez votre temps entre l'accueil, la salle d'attente et les différents bureaux des médecins ou professionnels du secteur social. Dans ce cadre, vos missions consistent à : Accueillir les patients, les informer et les orienter si besoin, Répondre aux appels téléphoniques et les transmettre si nécessaire, Analyser les demandes et évaluer les degrés d'urgence, Prendre les rendez-vous et gérer les plannings, organiser les réunions, Réaliser l'enregistrement informatique du dossier du patient, l'imprimer et le classer, Lancer les éditions (compte-rendu, note d'honoraires, etc.) et réaliser les envois, Gérer la facturation et la comptabilité courante, Gérer le courrier, effectuer l'archivage des documents, Gérer au quotidien la maintenance du système informatique, Mettre en œuvre, pour tous les correspondants et sous toutes ses formes, l'envoi des résultats. Alors, prêt(e) pour ce nouveau challenge ?

En tant qu’Assistant Médical (H/F), votre rôle et missions consistent à :- Accueillir les salariés et gérer les appels téléphoniques,- Assurer la gestion des agendas, la programmation des rendez-vous, - Assister les professionnels de l'équipe santé QVCT dans la gestion administrative quotidienne,- Préparer les fiches de renseignements des salariés et les documents permettant l'émission des fiches d'aptitudes et garantir la confidentialité des informations personnelles,- Gérer les facturations des actes médicaux,- Réaliser les tâches de secrétariat classique comme la rédaction des courriers et la gestion des appels téléphoniques, - Contribuer à l'amélioration des procédures administratives au sein de l'établissement,- Identifier les besoins en matériel et faire les commandes associées,- Ponctuellement, réalisation de supports de promotion de la sant,Alors, qu’en dites-vous ? Intéressé(e) ?

Konsult inom Medical Content, Copywriting & GEO till vår kund Har du erfarenhet av medicinsk kommunikation och förmågan att omsätta komplex medicinsk information till engagerande, lättillgängligt innehåll? Vi söker nu en konsult inom Medical Content, Copywriting och GEO för ett uppdrag hos en aktör inom digital hälsa – där du producerar och kvalitetssäkrar patientnära innehåll optimerat för både traditionell och AI-driven sökning. Om du kombinerar medicinsk förståelse med starka skrivkunskaper och ett öga för digital synlighet – kan detta vara uppdraget för dig. Om uppdraget Vår kund är en etablerad aktör inom hälsa och medicin med fokus på patientnära digitala lösningar. Du stödjer utvecklingen av innehåll inom ett specifikt terapiområde – innehållet ska vara medicinskt korrekt, målgruppsanpassat och optimerat för digital synlighet inklusive GEO och SEO. Ansvarsområden: Medicinsk kommunikation Tolka vetenskapliga publikationer, behandlingsriktlinjer och medicinska data. Producera och kvalitetssäkra innehåll som uppfyller regulatoriska krav och håller hög medicinsk korrekthet. Content & copywriting Skriva engagerande och pedagogiska texter för patienter och allmänhet. Anpassa budskap till olika målgrupper och digitala kanaler. Utveckla artiklar, patientguider, FAQ, webbtexter och kampanjmaterial. GEO & digital synlighet Strukturera innehåll för hög synlighet i både traditionella sökmotorer och AI-drivna sökupplevelser. Arbeta aktivt med GEO för att säkerställa att innehållet hämtas och prioriteras av generativa AI-sökmotorer och språkmodeller. Vi söker dig som Är självständig, proaktiv och van att driva projekt från strategi till konkret innehåll. Du har hög kvalitet i både medicinsk granskning och språk, strategisk förståelse för hur innehåll bidrar till patientutbildning och digital synlighet, samt god samarbetsförmåga i tvärfunktionella team. Krav och kvalifikationer Dokumenterad erfarenhet av medical writing eller medicinsk kommunikation God förståelse för ett eller flera terapiområden inom medicin och metabol hälsa Förmåga att tolka vetenskapliga publikationer, behandlingsriktlinjer och medicinska data Mycket god förmåga att skriva engagerande och pedagogiska texter för patienter och allmänhet Erfarenhet av att anpassa budskap till olika målgrupper och digitala kanaler Förståelse för GEO och hur generativa AI-sökmotorer hämtar och prioriterar innehåll Erfarenhet av att strukturera innehåll för synlighet i både traditionella och AI-drivna sökmiljöer Meriterande erfarenheter Erfarenhet från läkemedelsindustrin, medicinteknik, vårdgivare eller medicinsk kommunikationsbyrå Förståelse för regulatoriska krav och balanserad medicinsk kommunikation (LER) IMA-certifiering Erfarenhet av patientutbildande innehåll Erfarenhet från nordisk hälso- och sjukvård eller läkemedelsindustrin Plats och omfattning 100% omfattning, placering enligt överenskommelse. Resor i jobbet ingår. Ansökan För att söka uppdrag via Jappa behöver du skapa en konsultprofil på plattformen och skicka in din ansökan. Genom att göra detta blir din profil även synlig för andra uppdragsgivare som söker digitala, e-commerce- och kommersiella konsulter. Avsätt 10–15 minuter för att skapa din profil och bli aktuell för kommande uppdrag. Vi har ersatt gammelmäklare med en smart marknadsplats, branschkunskap, kvalitetssäkrade processer och AI. Resultatet är tydligare matchningar, snabbare besked och nöjdare både konsulter och kunder. Med Jappa blir det enkelt att hitta rätt uppdrag. Hos oss får du tillgång till en bred mix av möjligheter inom e-handel och tech – allt från kortare frilansuppdrag till längre engagemang och rekryteringar. Jappa är en talent-as-a-service-lösning där du som konsult står i centrum. Vi strävar alltid efter att matcha dig med uppdrag där du verkligen kan göra skillnad och utvecklas.

Head of Medical Scientific Affairs (ID2121\) The AO is a medically guided, not\-for\-profit organization, a global network of surgeons, and the world's leading education, innovation, and research organization specializing in the surgical treatment of trauma and musculoskeletal disorders. We are home to people from all over the world, from different backgrounds, with diverse talents and specialist areas. What binds us together is our passion for excellence, our dedication to our mission of improving patient care, and our understanding that we are stronger together: we are one AO. For more information, visit: / Head of Medical Scientific Affairs (ID2121\) Short Description The Head of Medical Scientific Affairs provides strategic and scientific leadership for AO's clinical evidence generation ecosystem and ensures that clinical research investments translate into meaningful improvements in patient care. He/she serves as a trusted scientific advisor to AO leadership, governance committees, and clinical divisions and represents AO ITC in internal and external scientific initiatives, partnerships, and expert forums. The role is accountable for developing a high\-impact portfolio of clinical studies across Trauma, CMF, Spine,TC, Veterinary, and related orthopedic disciplines, ensuring optimal allocation of resources, scientific excellence, and supporting effective translation of evidence into clinical practice. The position serves as a key interface between surgeons, researchers, clinical operations, governance bodies, industry partners, and educational stakeholders to maximize the generation, dissemination, and adoption of evidence\-based innovations within the AO ecosystem. Main Responsibilities Lead the Medical Scientific Affairs team Provide scientific, strategic and operational leadership to the Medical Scientific Affairs team with two direct reports, fostering a high\-performing, collaborative, and service\-oriented culture. Define team objectives, priorities, and performance expectations aligned with the organization's strategy and portfolio needs. Recruit, develop, coach, and evaluate team members to support professional growth, ensuring the appropriate scientific, clinical, and operational competencies are in place. Close collaboration with Clinical Operations in the resource planning and allocation across studies, programs, and stakeholder requests to meet organizational objectives. Build effective collaboration between surgeons, governance bodies, Clinical Operations, NCR, AO Education Institute, AO Research Institute, educators, and external partners to advance the Clinical Research activities in the AO. Drive continuous improvement of Medical Scientific Affairs processes, standards, and capabilities to enhance quality, efficiency, and impact and establish a culture of scientific excellence, integrity, compliance, and evidence\-based decision\-making across all Medical Scientific Affairs activities. Lead the Clinical Science Advisory Commission (CSAC). Lead the AO ITC Clinical Research Fellowship Program. Support the AO PEER program. Clinical Study Design \& Scientific Support Develop clinical study protocols addressing important knowledge gaps and clinical needs in close collaboration with surgeons, industry partners, governance bodies and Network Clinical Research and Clinical Operations. Review and provide medical\-scientific assessment of adverse events and safety\-related findings throughout study conduct. Provide expert advice on medical and scientific questions arising during study execution and support preparation of scientific publications, clinical reports, congress abstracts, and other dissemination activities. Close collaborate with Clinical Operations in study planning, implementation, and monitoring activities. Support interpretation of results in close collaboration with surgeons, investigators, governance bodies, and Clinical Operations. Drive excellence in scientific publication strategies, congress presentations, and dissemination activities. Clinical Research Portfolio Strategy Lead scientific discussions regarding future evidence needs. Develop and maintain a strategic clinical research portfolio in collaboration with the Research Commissions and internal stakeholders which is aligned with AO's mission and priorities. Establish and continuously refine portfolio prioritization frameworks balancing available research funding, knowledge gaps, patient impact, scientific significance, feasibility, cost\-effectiveness and translational potential and risk\-benefit considerations in collaboration with the Research Commissions and internal stakeholders. Monitor portfolio performance with regards to strategic objectives and adapt research priorities based on emerging evidence, and clinical needs. Provide scientific leadership across the full research lifecycle, ensuring methodological rigor, clinical relevance, regulatory compliance, and ethical conduct. Collaborate with Clinical Operations in establishing a grant acquisition strategy and strengthen industry partnerships and drive grant acquisition. Support Knowledge Translation activities to ensure clinical evidence generated by AO is effectively translated into education, clinical guidelines, decision support tools, and clinical practice. Collaborate closely with Clinical Operations, NCR, AO Education, AO Clinical Divisions, community development and governance bodies to facilitate adoption of new evidence. Lead implementation of health economic and outcomes research initiatives. Main Requirements Professional \& Technical Skills Advanced expertise in clinical research methodology. Strong understanding of orthopedic clinical practice and research. Advanced expertise in clinical study design, statistical principles, and evidence synthesis. Experience in designing and executing industry sponsored clinical studies as a CRO. Experience in health economic evaluation and outcomes research. Excellent scientific grant and publication writing and presentation skills. Sound understanding of regulatory requirements, Good Clinical Practice (GCP), and clinical research governance. Education \& Qualifications Medical Degree (MD) required. PhD, MSc, or equivalent advanced scientific qualification highly desirable. Formal training in clinical epidemiology, research methodology, biostatistics, or related disciplines is advantageous. Professional Experience Minimum 10 years of experience in clinical research within orthopedics, trauma, spine, CMF, sports medicine, or related disciplines. Experience in multicenter clinical studies from concept generation to publication and dissemination. Experience in developing and managing research portfolios and clinical research strategies. Strong track record of peer\-reviewed scientific publications and grant acquisition. Experience in line management and leading interdisciplinary and cross\-functional teams. Demonstrated ability to collaborate effectively with surgeons and international clinical research networks. CRO services are of advantage. An interesting and varied job in an exciting and innovative organization The opportunity to be part of a highly committed international team Modern infrastructure High degree of flexibility regarding working hours and location (depending on operational requirements) Generous pagacke of social benefits, including supplementary vacation days and pension scheme contributions Internal skills training opportunities and support for continued education jpidfa7c62ajm jit0730jm jiy26jm

Möchtest du mit deiner Expertise in den Bereichen Qualitätsmanagement und Arzneimittelsicherheit einen nachhaltigen Beitrag zur Patientenversorgung leisten? Wir sind ein moderner, gesamtschweizerisch tätiger Dienstleister im Homecare\-Bereich. Unser innovatives Betreuungskonzept richtet sich an Menschen mit seltenen Erkrankungen, die langfristig auf spezialisierte medikamentöse Therapien angewiesen sind und diese sicher in ihrem privaten Umfeld erhalten möchten. Zur Ergänzung unseres Teams suchen wir ab sofort oder nach Vereinbarung eine qualitätsbewusste Persönlichkeit als Manager Medical Quality 80% Deine Aufgaben Qualitätsmanagement Mitarbeit bei der Weiterentwicklung und Pflege des Qualitätsmanagementsystems Erstellung, Prüfung und Aktualisierung von SOPs und anderen qualitätsrelevanten Dokumenten Bearbeitung von Abweichungen, Reklamationen sowie CAPAs Unterstützung bei internen Schulungen zu Qualitäts\- und Sicherheitsprozessen Mitarbeit an interdisziplinären Projekten (z. B. Einführung neuer Therapien, Prozessoptimierungen, Digitalisierung) Pharmakovigilanz Mitverantwortung für die Erfassung und Dokumentation von Nebenwirkungsmeldungen Sicherstellung der PV\-Compliance gemäss Vorgaben, insbesondere im Zusammenhang mit Pharma\-unterstützten Patientenunterstützungsprogrammen Ansprechperson für interne und externe Anfragen zur Pharmakovigilanz Mitwirkung bei PV\-relevanten Audits und internen Reviews Das bringst du mit Ausbildung im Life Science Bereich (z. B. Pharmazie, Naturwissenschaften, Medizin o.ä.) Berufserfahrung in Pharmakovigilanz und/oder Qualitätsmanagement, idealerweise im Pharma\-Umfeld Gute Kenntnisse regulatorischer Anforderungen in den Bereichen Arzneimittelsicherheit und Qualitätsmanagement Sehr gute Deutschkenntnisse in Wort und Schrift, gute ösisch\- und Englischkenntnisse Analytische, strukturierte und selbständige Arbeitsweise Hohes Qualitäts\- und Verantwortungsbewusstsein Freude an interdisziplinärer Zusammenarbeit IT\-Affinität und sicherer Umgang mit digitalen Dokumentationssystemen Wir bieten dir Eine sinnstiftende Tätigkeit an der Schnittstelle von Arzneimittelsicherheit, Qualitätsmanagment und Patientenversorgung 80 %\-Pensum mit flexiblen Arbeitszeiten (Jahresarbeitszeit) Mindestens 5 Wochen Ferien, ab dem 50\. Lebensjahr 6 Wochen Förderung deiner fachlichen Weiterentwicklung Ein engagiertes, interdisziplinäres Team mit kurzen Entscheidungswegen Gestaltungsspielraum und Entwicklungsmöglichkeiten innerhalb unserer Organisation Erkennst du dich in dieser Stelle? Dann sende uns deine vollständigen Unterlagen mit Foto per Mail an [E\-Mail schreiben](<>). Fragen zur Stelle beantwortet dir gerne Camenzind, Head Human Resources, . Weitere Informationen findest du auf unserer Homepage . jpida57e4b9jm jit0730jm jiy26jm

Project Manager Medical Simulation (ID1940\) The AO is a medically guided, not\-for\-profit organization, a global network of surgeons, and the world's leading education, innovation, and research organization specializing in the surgical treatment of trauma and musculoskeletal disorders. We are home to people from all over the world, from different backgrounds, with diverse talents and specialist areas. What binds us together is our passion for excellence, our dedication to our mission of improving patient care, and our understanding that we are stronger together: we are one AO. For more information, visit: / Project Manager Medical Simulation (ID1940\) Short Description As Project Manager \- Medical Simulation, you will bridge the gap between practical execution and strategic vision, ensuring our simulation\-based education programs maintain the highest standards while evolving to meet future needs. You will be instrumental in bringing cutting\-edge simulation technologies to healthcare professionals around the world. Main Responsibilities Operational Management Execute the setup, operation, and maintenance of simulation equipment for international training events Manage biological specimen handling and logistics in compliance with international regulations Coordinate logistical aspects of simulation\-based training events in Davos and support global locations Oversee import/export requirements for specialized training materials Maintain and organize simulation equipment, tools, and supplies inventory Project Implementation Implement simulation\-based training projects from planning to delivery Track project milestones, timelines, and deliverables Resolve operational challenges during project execution Document processes and outcomes to support continuous improvement Coordinate cross\-functional team activities to achieve project goals Technology \& Innovation Support the evaluation of novel, simulation\-based learning experiences Contribute to the development and go2market of digital simulation tools Assist in managing relationships with technology and service partners Provide input on scalability opportunities for simulation programs Help implement emerging technologies in simulation education Main Requirements Experience \& Qualifications Bachelor's degree in healthcare, education, project management, or related field 3\-5 years of experience in medical education, simulation operations, clinical laboratories or related field Proven experience managing complex projects with operational components Experience with medical simulation technologies (preferred) Human anatomical specimen lab technician experience is a must Skills \& Competencies Excellent logistical planning and coordination abilities Strong project execution and follow\-through Effective communication across diverse stakeholder groups Technical aptitude for working with simulation equipment Resilient and solution\-focused under time or resource pressure Fluency in English is a must, German is a strong asset Comfortable with international travel (approximately 10%) Personal Attributes Pragmatic problem\-solver with a "roll up your sleeves" mentality Balance of operational detail\-orientation with strategic thinking Resilience and adaptability in fast\-paced environments Openness to new technologies and methodologies Passion for medical education and improving patient care globally An interesting and varied job in an exciting and innovative organization The opportunity to be part of a highly committed international team Modern infrastructure High degree of flexibility regarding working hours and location (depending on operational requirements) Generous pagacke of social benefits, including supplementary vacation days and pension scheme contributions Internal skills training opportunities and support for continued education jpid2fcb0ccjm jit0729jm 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 now SIGVARIS AG \- Gröblistrasse 8 \- 9014 St. Gallen jpid4159160jm jit0729jm jiy26jm

Digital Solutions Medical Affairs Agap2 est un groupe européen d’ingénierie et de conseil opérationnel fondé en 2005 et spécialisé dans l’industrie. Nous travaillons dans les secteurs de la pharmacie, de la biotechnologie, des dispositifs médicaux, de l’horlogerie et de la mécanique de précision. En tant que consultant, vous serez amené à accompagner nos clients dans la réalisation de leurs projets sur site en apportant votre expertise et vos compétences. Vous êtes agile et désireux de vous adapter à différents environnements de travail qui alimenteront votre curiosité de voir ce qui se cache derrière les portes fermées des plus grands projets du portefeuille de nos clients. Digital Solutions Medical Affairs ?? Vos missions • Administrer et faire évoluer les plateformes Veeva (CRM, Vault MedComms, PromoMats, MedInquiry). • Piloter des projets de déploiement, migration et intégration de systèmes. • Recueillir les besoins métiers et les traduire en solutions techniques performantes. • Collaborer avec les équipes internationales, les partenaires IT et les fournisseurs. • Participer à des initiatives innovantes autour de l'IA appliquée aux contenus et processus médicaux. • Assurer le support, la gouvernance et l'amélioration continue des outils. ?? Votre profil • 2 à 5 ans d'expérience minimum dans l'administration de systèmes et la gestion de projets au sein de l'industrie pharmaceutique, biotech ou Life Sciences. • Solide expérience des solutions Veeva (CRM, Vault, MedInquiry). • Bonne compréhension des processus Medical Affairs et des environnements réglementés (GxP/CSV). • Expérience de projets internationaux et gestion de multiples parties prenantes. • Anglais courant indispensable. Le français constitue un atout. jpidfe501a4jm jit0729jm jiy26jm

Agap2 est un groupe européen d’ingénierie et de consei Digital Solutions Medical Affairs Agap2 est un groupe européen d’ingénierie et de conseil opérationnel fondé en 2005 et spécialisé dans l’industrie. Nous travaillons dans les secteurs de la pharmacie, de la biotechnologie, des dispositifs médicaux, de l’horlogerie et de la mécanique de précision. En tant que consultant, vous serez amené à accompagner nos clients dans la réalisation de leurs projets sur site en apportant votre expertise et vos compétences. Vous êtes agile et désireux de vous adapter à différents environnements de travail qui alimenteront votre curiosité de voir ce qui se cache derrière les portes fermées des plus grands projets du portefeuille de nos clients. Digital Solutions Medical Affairs ?? Vos missions • Administrer et faire évoluer les plateformes Veeva (CRM, Vault MedComms, PromoMats, MedInquiry). • Piloter des projets de déploiement, migration et intégration de systèmes. • Recueillir les besoins métiers et les traduire en solutions techniques performantes. • Collaborer avec les équipes internationales, les partenaires IT et les fournisseurs. • Participer à des initiatives innovantes autour de l'IA appliquée aux contenus et processus médicaux. • Assurer le support, la gouvernance et l'amélioration continue des outils. ?? Votre profil • 2 à 5 ans d'expérience minimum dans l'administration de systèmes et la gestion de projets au sein de l'industrie pharmaceutique, biotech ou Life Sciences. • Solide expérience des solutions Veeva (CRM, Vault, MedInquiry). • Bonne compréhension des processus Medical Affairs et des environnements réglementés (GxP/CSV). • Expérience de projets internationaux et gestion de multiples parties prenantes. • Anglais courant indispensable. Le français constitue un atout. jpid76c3192jm jpit0729jm jpiy26jm

In order to work in Ireland a non-EEA National, unless they are exempted, must hold a valid employment permit. Please review the Eligibility and requirements for an employment permit if you are unsure of your eligibility to apply for this vacancy.
Post ID: 039273 Post Summary:- The Discipline of Medical Education in the School of Medicine at Trinity College invites applications for the post of Assistant Professor in Medical Education with a particular focus on clinical education, the development of high-quality clinical learning experiences for students, and the building of networks of clinical educators across partner healthcare sites. The postholder will play a key role in the design, delivery, evaluation and enhancement of workplace-based learning across the undergraduate and internship continuum, ensuring alignment with university policy, international best practice, and the standards of the Irish Medical Council. The successful applicant will have an established or emerging reputation in teaching, faculty development, and educational scholarship, and will contribute to curriculum review with particular emphasis on clinical placements, longitudinal integrated clerkships, internship preparation, and transitions into postgraduate training. Appointees will divide their time between teaching, educational research, and leadership of initiatives that support clinical supervisors, clinical tutors, and teaching hospitals in delivering excellent learning experiences. The postholder will play a critical role in strengthening partnerships between the School of Medicine and its affiliated clinical sites, and in developing sustainable communities of practice among clinical educators. Post status: 2 Year Fixed-Term Contract This employment is for the specific purpose of supporting the development of clinical placements across affiliated sites and delivering identified short- to medium-term strategic objectives in medical education and clinical training. This employment is not offered on an indefinite duration basis as it is aligned to a fixed-term requirement to support curriculum reform and the development of clinical education initiatives within the School of Medicine. Hours of Post: Hours of work for academic staff are those as prescribed under Public Service Agreements. For further information please follow the link below: http://www.tcd.ie/hr/assets/pdf/academic-hours-public-service-agreement.pdf Salary: This appointment will be made on the Assistant Professor Salary Scale (€43,859 - €104,618 per annum) at a point in line with current Government pay policy. monthly/weekly payscales. (tcd.ie) Closing Date: 12 Noon Irish Standard Time, 4th August 2026 How to apply: To assist the selection process, applicants should submit; Cover Letter (1x A4 page) A comprehensive curriculum vitae, including a full list of publications The names and contact details (i.e. addresses, e-mail, etc.) of three referees A comprehensive research plan (maximum 2 pages) and a teaching statement (maximum 2 pages) Please note: Applicants who do not submit the above will not be considered at the short list stage Applicants should note that the interview process for this appointment will include the deliver