field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

Wir suchen für unseren renommierten Kunden im medizintechnischen Bereich für Innsbruck ab sofort einen Clinical Research Mitarbeiter (m/w/d)Deine Aufgaben:<ul><li>Überwachung und Kontrolle von klinischen Studien</li><li>Austausch mit Behörden und externen Stellen</li><li>Beiträge zu Publikationen </li><li>Dokumentationen </li><li>Projektbetreuung</li></ul>Dein Profil:<ul><li>abgeschlossene Ausbildung im naturwissenschaftlichen Bereich (Biologie, Medizin, Pharmazie oder vergleichbares)</li><li>mindestens 2 Jahre Erfahrung als "Clinical Research Manager" </li><li>Erfahrung mit Medizinprodukten und das Wissen über die dazugehörigen behördlichen und gesetzlichen Vorschriften </li><li>Sehr gute Englischkenntnisse</li></ul>Was wir bieten:<ul><li>attraktives und sicheres berufliches Umfeld - Direktanstellung beim Kunden - kein Leasing!</li><li>Mitarbeit in einem engagierten und motivierten Team</li><li>Diverse Mitarbeitervorteile (z.B. Mitarbeiter Discounts, Mitarbeiterprogramme,)</li><li>flexible Arbeitszeiteinteilung</li></ul>Aus gesetzlichen Gründen weisen wir daraufhin, dass das kollektivvertragliche Mindestgehalt für diese Position bei € 2890,- brutto pro Monat liegt. Die tatsächlichen Gehaltspakete orientieren sich an aktuellen Marktgehältern und berücksichtigen deine Qualifikation und Erfahrung. Das Stellenprofil hat dich angesprochen? Dann schick uns deine Bewerbung!

Randstad Innsbruck

Clinical Research Mitarbeiter (m/w/d)

Im Bereich Analytical Development PDT sind wir für die analytische Unterstützung der Produktentwicklung verantwortlich und gewährleisten die Produktqualität unserer Plasma-Produkte über deren gesamten Lebenszyklus. Unser Fokus liegt auf der Entwicklung und Implementierung innovativer analytischer Methoden in die routinemäßige Testung.Research Associate CMC (m/w/d) - Befristete Vakanzvertretung im Bereich Analytical Development PDT (1 Jahre) Standort: Wien Startdatum: ab sofort Wochenstunden: 38 - ALL INZur Verstärkung unseres Teams suchen wir ab sofort einen engagierten und motivierten Senior Research Associate (m/w/d) für eine befristete Vakanzvertretung von 1 Jahr, der mit Leidenschaft unsere hohen Qualitätsstandards unterstützt.Deine Aufgaben:<ul><li>Durchführung analytischer Tests an Plasmaproben und Intermediaten (z. B. UV-Spektroskopie, ELISA, HPLC, SDS-PAGE, Western Blotting).</li><li>Erstellung und Aktualisierung abteilungsinterner Testvorschriften und SOPs.</li><li>Unterstützung bei der Erstellung und Durchführung von Qualifizierungsplänen.</li><li>Organisatorische Aufgaben zur Sicherstellung eines reibungslosen Laborbetriebs.</li><li>Verantwortung für die Wartung und Pflege von Laborgeräten.</li><li>Technische Betreuung und Unterstützung von Praktikanten.</li></ul>Was wir bieten:<ul><li>Zertifiziertes familienfreundliches Unternehmen (umfassende Wiedereinstiegsmodelle nach der Karenz)</li><li>Hybrides Arbeiten &amp; flexible Zeiteinteilung wo möglich</li><li>Weiterbildungs- und -entwicklungsmöglichkeiten</li><li>Umfassende Trainings- und Fortbildungsprogramme sowie Persönlichkeitsentwicklung und Mentoringprogramm</li><li>Firmeninterne Job Rotations im In- und Ausland</li><li>Mitarbeiter*innenempfehlungs- und -anerkennungsprogramme</li><li>Aktive Teilnahme an Netzwerkgruppen zu verschiedenen Themen (z.B. Diversity, Equity &amp; Inclusion, Nachhaltigkeit)</li><li>Vielfältige Gesundheits- und Fitnessangebote</li><li>Kostenlose Impfungen, Psychologische Beratung</li><li>Firmen-Events &amp; Feste</li><li>Betriebsrat</li><li>Betriebsrestaurant zu gestützten Preisen</li><li>Bilingualer Betriebskindergarten / Betriebliche Kinderbetreuung</li><li>Gute öffentliche Anbindung</li><li>Inhouse Fitness &amp; Wellness Center in Wien</li></ul><h3>Zusätzliche Informationen:</h3>Das Mindestgehalt beträgt 4.963 € brutto pro Monat (gemäß Kollektivvertrag der chemischen Industrie). Eine Überzahlung ist je nach Qualifikation und Erfahrung möglich.

Senior Research Associate (Vakanzvertretung) (m/w/d)

Description Local Contractor Research Nurse (Per Diem) - Innsbruck, Austria Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. These include mobile research nursing, patient concierge, medical photography and clinical research services. Illingworth are experts with experience across all study phases and in a diverse range of therapeutic areas. Illingworth Research Group is a global organization operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives. Job Responsibilities <ul><li>Support patients participating in clinical research studies by coordinating care and facilitating communication with healthcare providers</li><li>Help patients understand study protocols, schedule appointments, and address concerns related to their participation</li><li>Collaborate with research teams to monitor patient progress and collect data while ensuring compliance with regulatory standards</li><li>Serve as a resource to help patients navigate the healthcare system and access necessary services throughout their research experience</li><li>Ensure that participants remain engaged and compliant with study protocols to maintain the integrity and validity of the research</li><li>Contribute to the overall efficiency and effectiveness of the research process by coordinating care and facilitating communication between patients and healthcare providers</li><li>Ensure that patient data is accurately collected and monitored to enhance the quality of the research outcomes</li><li>May be responsible for entire projects or processes within their area of responsibility, contributing to the design, implementation, and delivery of processes, programs, and policies</li></ul>Qualifications: <ul><li>Bachelor's degree in Nursing or a related field</li><li>Minimum of 3 years of experience in clinical research or patient care</li><li>Strong understanding of clinical research protocols and regulatory standards</li><li>Excellent communication and interpersonal skills</li><li>Ability to work independently and as part of a team</li></ul>Certifications: <ul><li>Registered Nurse (RN) license</li><li>Certification in Clinical Research (e.g., CCRP, CCRC) preferred</li></ul>Necessary Skills: <ul><li>In-depth knowledge and skills within the professional discipline of clinical research and patient care</li><li>Ability to coordinate care and facilitate communication between patients and healthcare providers</li><li>Strong organizational and time management skills</li><li>Ability to address patient concerns and provide individualized support</li><li>Proficiency in data collection and monitoring</li><li>Understanding of the impact of work on related areas and the ability to manage processes and programs</li></ul>Additional Information: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Summary Roles within the Research Nurse/Patient Concierge job family at the P22 level are responsible for supporting patients participating in clinical research studies by coordinating care and facilitating communication with healthcare providers. These roles help patients understand study protocols, schedule appointments, and address concerns related to their participation. They collaborate with research teams to monitor patient progress and collect data while ensuring compliance with regulatory standards. They serve as a resource to help patients navigate the healthcare system and access necessary services throughout their research experience. Impact and Contribution Roles within the Research Nurse/Patient Concierge job family at the P22 level play a crucial part in the success of clinical research studies. By providing comprehensive support to patients, they ensure that participants remain engaged and compliant with study protocols, which is essential for the integrity and validity of the research. Their efforts in coordinating care and facilitating communication between patients and healthcare providers contribute to the overall efficiency and effectiveness of the research process. Additionally, their collaboration with research teams helps to ensure that patient data is accurately collected and monitored, further enhancing the quality of the research outcomes. These roles require in-depth knowledge and skills within the professional discipline of clinical research and patient care, as well as an understanding of the impact of their work on related areas. Roles within the Research Nurse/Patient Concierge job family at the P22 level may be responsible for entire projects or processes within their area of responsibility, contributing to the design, implementation, and delivery of processes, programs, and policies. Core Focus • Providing individualized support to patients participating in clinical research studies • Coordinating care and facilitating communication with healthcare providers • Helping patients understand study protocols and addressing their concerns • Scheduling appointments and ensuring patients adhere to study timelines • Collaborating with research teams to monitor patient progress and collect data • Ensuring compliance with regulatory standards and maintaining the integrity of the research • Serving as a resource to help patients navigate the healthcare system and access necessary services

Local Contractor Research Nurse (Per Diem) - Innsbruck, Austria

Description Local Contract Research Nurse (Per Diem) - Weyer, Austria Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. These include mobile research nursing, patient concierge, medical photography and clinical research services. Illingworth are experts with experience across all study phases and in a diverse range of therapeutic areas. Illingworth Research Group is a global organization operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives. Job Responsibilities <ul><li>Support patients participating in clinical research studies by coordinating care and facilitating communication with healthcare providers</li><li>Help patients understand study protocols, schedule appointments, and address concerns related to their participation</li><li>Collaborate with research teams to monitor patient progress and collect data while ensuring compliance with regulatory standards</li><li>Serve as a resource to help patients navigate the healthcare system and access necessary services throughout their research experience</li><li>Ensure that participants remain engaged and compliant with study protocols to maintain the integrity and validity of the research</li><li>Contribute to the overall efficiency and effectiveness of the research process by coordinating care and facilitating communication between patients and healthcare providers</li><li>Ensure that patient data is accurately collected and monitored to enhance the quality of the research outcomes</li><li>May be responsible for entire projects or processes within their area of responsibility, contributing to the design, implementation, and delivery of processes, programs, and policies</li></ul>Qualifications: <ul><li>Bachelor's degree in Nursing or a related field</li><li>Minimum of 3 years of experience in clinical research or patient care</li><li>Strong understanding of clinical research protocols and regulatory standards</li><li>Excellent communication and interpersonal skills</li><li>Ability to work independently and as part of a team</li><li>Within 3 hours of Vienna, Austria</li></ul>Certifications: <ul><li>Registered Nurse (RN) license</li><li>Certification in Clinical Research (e.g., CCRP, CCRC) preferred</li></ul>Necessary Skills: <ul><li>In-depth knowledge and skills within the professional discipline of clinical research and patient care</li><li>Ability to coordinate care and facilitate communication between patients and healthcare providers</li><li>Strong organizational and time management skills</li><li>Ability to address patient concerns and provide individualized support</li><li>Proficiency in data collection and monitoring</li><li>Understanding of the impact of work on related areas and the ability to manage processes and programs</li></ul>Additional Information: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Summary Roles within the Research Nurse/Patient Concierge job family at the P22 level are responsible for supporting patients participating in clinical research studies by coordinating care and facilitating communication with healthcare providers. These roles help patients understand study protocols, schedule appointments, and address concerns related to their participation. They collaborate with research teams to monitor patient progress and collect data while ensuring compliance with regulatory standards. They serve as a resource to help patients navigate the healthcare system and access necessary services throughout their research experience. Impact and Contribution Roles within the Research Nurse/Patient Concierge job family at the P22 level play a crucial part in the success of clinical research studies. By providing comprehensive support to patients, they ensure that participants remain engaged and compliant with study protocols, which is essential for the integrity and validity of the research. Their efforts in coordinating care and facilitating communication between patients and healthcare providers contribute to the overall efficiency and effectiveness of the research process. Additionally, their collaboration with research teams helps to ensure that patient data is accurately collected and monitored, further enhancing the quality of the research outcomes. These roles require in-depth knowledge and skills within the professional discipline of clinical research and patient care, as well as an understanding of the impact of their work on related areas. Roles within the Research Nurse/Patient Concierge job family at the P22 level may be responsible for entire projects or processes within their area of responsibility, contributing to the design, implementation, and delivery of processes, programs, and policies. Core Focus • Providing individualized support to patients participating in clinical research studies • Coordinating care and facilitating communication with healthcare providers • Helping patients understand study protocols and addressing their concerns • Scheduling appointments and ensuring patients adhere to study timelines • Collaborating with research teams to monitor patient progress and collect data • Ensuring compliance with regulatory standards and maintaining the integrity of the research • Serving as a resource to help patients navigate the healthcare system and access necessary services

4 Wissenschaft / Forschung Vollzeit Jobs