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Description 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

Research Nurse (Per Diem) - Innsbruck, Austria

Description Research Nurse (Per Diem) - Vienna, 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

Research Nurse (Per Diem) - Vienna, Austria

<h1>Mikrobiologe Wasserhygiene (m/w/d)</h1><a href="https://www.isg.com/jobs/applications/applyForJobEntry.jsf?inseratnummer=107508&amp;refererId=625" target="_blank">APPLY</a>Interessante TätigkeitFlexible ArbeitszeitenWeiterentwicklungGute AnbindungFamilienfreundlichkeitUnser Kunde ist einer der Marktführer seines Segments, wirtschaftlich erfolgreich und sehr etabliert. 
 Zur Verstärkung wird am Standort in Wels eine weitere Position besetzt: 
 Bist Du die gesuchte Person, die im Labor unseres Kunden eine berufliche Heimat findet?Aufgaben: 
<ul> 
 <li>Durchführung mikrobiologischer Untersuchungen von Wasser</li> 
 <li>Heizwasseranalysen nach technischen Richtlinien</li> 
 <li>Erstellung von Prüfberichten</li> 
 <li>Auswertung bzgl. Legionellen</li> 
 <li>Ansprechpartner für Behörden, technische Partner und Kunden</li> 
</ul> Profil: 
<ul> 
 <li>Abgeschlossenes Studium der Biologie, Mikrobiologie oder ähnlicher Fachrichtungen</li> 
 <li>Erfahrung in der mikrobiologischen Wasseranalytik</li> 
 <li>Kenntnisse von relevanten Vorschriften und Normen</li> 
 <li>Kenntnisse mit Nachweisverfahren wie Kultivierung</li> 
 <li>Hohes Qualitätsbewusstsein</li> 
 <li>Selbständige Arbeitsweise</li> 
</ul> Diese Position wird mit einem Grundgehalt von rund EUR 50.000,- dotiert (Überzahlung je nach Ausbildung und beruflicher Erfahrung). 
 Wenn Sie an dieser herausfordernden Position Interesse haben, dann freuen wir uns über Ihre aussagekräftige Bewerbung unter der Kennnummer 107&nbsp;508 bevorzugt über unser <a href="https://www.isg.com/jobs/applications/applyForJobEntry.jsf?inseratnummer=107508&amp;refererId=625" target="_blank">ISG-Karriereportal</a> oder per E-Mail. 
Besuchen Sie uns auf <a href="https://www.isg.com/jobs/search" target="_blank">isg.com/jobs</a> - hier finden Sie täglich neue Jobangebote.<a href="https://www.isg.com" target="_blank"></a>ISG Personalmanagement GmbH 
 A-1010 Wien, Universitätsring 14 
 Renate Schobesberger, MAS, M: +43 676 704 25 14 
 @:<a href="mailto:bewerbung.schobesberger@isg.com" target="_blank"> bewerbung.schobesberger@isg.com</a>

ISG Personalmanagement GmbH

Wir sind die ISG

Mikrobiologe (m/w/d)

Research Associate | Senior Research Associate | Lab Investigator Our client Takeda Pharmaceutical Company Limited is a leading global, value-driven, research-based biopharmaceutical company headquartered in Japan. In Austria, Takeda operates along the entire pharmaceutical value chain: research &amp; development, plasma application, manufacturing and distribution. Takeda is the largest pharmaceutical employer in Austria. Every day, around 4,500 employees help to ensure that medicines from Austria reach the whole world and that patients in Austria have access to innovative medicines from Takeda. The Austrian product portfolio helps patients in the fields of oncology, hemophilia and genetic diseases, gastroenterology and immunology, among others. Come join our team fixed-term for 3 months for the opportunity to make an impact on patients' lives. <h3>Your Accountabilites</h3><ul><li>Preparation and execution of process development lab and pilot scale studies applying general preparative purification methods such as chromatography, filtration (depth filtration, membrane filtration, …), precipitations, centrifugations, and virus clearance steps.</li><li>Maintenance of established methods and supporting development of alternative methods, when key reagents are no longer available</li><li>Implementation of new equipment and equipment upgrades in the lab environment (new technology evaluation) (for Sr. Research Associates and Lab Investigaors only)</li><li>Independent planning, accurate performing, critical analyzing, diligent documenting of experimental work</li><li>Preparation and support study plan and study report generation (for Lab Investigators only)</li><li>Lab organization to ensure quality and to keep lab technology at industry best-in-class standard</li></ul><h3>Your Qualifications</h3><ul><li>HTL degree, bachelor or master degree of chemistry, biochemistry, biology, biotechnology, chemical/process engineering or related fields is required</li><li>Experience in laboratory work within the last years in life sciences</li><li>Knowledge of laboratory related quality and safety guidelines</li><li>Scientific knowledge in process development and about plasma derived therapies fractionation and purification processes beneficial</li><li>Technically skilled and mostly independent, diligent, and proactive workstyle</li><li>Critical thinking and problem solving skills</li><li>Knowledge of state of the art technologies within the scientific community in life sciences</li><li>Good communication, organization, and time management skills</li></ul><h3>Beneficial skills</h3><ul><li>The incumbent must be creative, courageous, collaborative, solution-focused and work mostly independent.</li><li>Willingness to limited weekend duties required.</li><li>External communication with vendors, customers, service providers and collaborators as required to fulfill the assigned technical tasks</li><li>Willingness to work at lab and pilot scale at ambient and cooled temperatures during experimental setups.</li></ul>At Takeda, we are transforming the pharmaceutical industry through our R&amp;D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Takeda encourages and supports its employees by trainings, job rotations and mentoring. A balanced work - life ratio (recognition for work and family, company kindergarten) and numerous benefits (fitness center, cafeteria, etc.) complete our profile as a top employer. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Gender, age, skin color, background or sexual orientation play no role in this as we actively promote diversity. We equally address people with disabilities. In the course of a recruitment process which is as free of barriers as possible, we encourage you to mention all relevant information in this context in your application. Motivated employees must be remunerated appropriately.The minimum salary for the following positions is:<ul><li>Reserach Associate € 3,600.00 gross per month</li><li>Sr. Research Associate € 4,655 gross per month</li><li>Lab Investigator € 4,850 gross per month</li></ul>Based on your professional experience and qualifications, a higher salary is envisaged. The contract is limited till September 2025.The actual remuneration package will be guided by your professional experience and your qualifications, so increased payment is possible. Facts <ul><li>AUT - Vienna</li><li>Employee</li><li>Fixed Term (Fixed Term)</li><li>Full time or All-In, depending on level</li></ul>

Research Associate / Lab Investigator (m/w/d)

<ul><li>Projektleitungsfunktion für den Produktentwicklungsprozess vom Prototyp bis Vorserie</li><li>Weiterentwicklung der Produktlinien anhand dynamischer Marktanforderungen</li><li>Begleitung von Teststellungen von Maschinen im Feld</li><li>Projektabstimmung mit Endkunden und Zulieferern</li><li>Machbarkeitsanalysen von innerbetrieblichem Vorschlagswesen</li><li>Terminkoardinaton der einzelnen Projekten</li><li>Leitung vom Simultanen Eingineering Runden</li></ul><ul><li>HTL Maschinenbau oder Elektrotechnik / Studienabschluss Uni / FH Maschinenbau/Elektrotechnik</li><li>Mehrjährige Berufserfahrung in vergleichbarer Position (mind. 3 Jahre)</li><li>Grundkenntnisse in 3D-CAD Systemen (Solid Edge)</li><li>Solide Projektmanagementerfahrung</li><li>Hohes Maß an Kommunikations- &amp; Teamfähigkeit und Durchsetzungsvermögen</li><li>Eigenständige, lösungsorientierte &amp; strukturierte Arbeitsweise</li><li>Gute Englischkenntnisse in Wort &amp; Schrift</li></ul>

5 Jobs in Wissenschaft & Forschung