54 Jobs für Research Study Coordinator
Stellenangebote Research Study Coordinator Jobs
Job vor 3 Tagen bei Jooble gefunden
Kantonsspital Aarau AG
• Schweiz
# # #BL/ BL # # # Clinical
Research Coordinator (Datamanagement) Clinical Research Coordinator (Datamanagement) KSA Kinderspital Aarau, Pädiatrische Hämatologie und Onkologie Startdatum Ab 1. April 2026 oder nach Vereinbarung, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] unbefristet Pensum 40-60 Arbeitsort Aarau Ihre Aufgaben Koordination/ Datamanagement von klinischen Studien und wissenschaftlichen Projekten am Universitären Zentrum für Pädiatrische Hämatologie und Onkologie Nordwestschweiz, Standort Kinderspital Kantonsspital Aarau Vorbereitung, [. .. ] u. a. ) Ihr Profil Ausbildung/ Tätigkeit im Gesundheitswesen (z. B. Pflegefachperson, MPA) , naturwissenschaftlicher Hintergrund (z. B. Biomedizin, Phar-mazie) oder Qualitätsmanagement Weiterbildung/ Erfahrung als Clinical Research Coordinator oder Study Nurse von Vorteil Sorgfältige, zuverlässige und selbständige Arbeitsweise Sicherer Umgang mit digitalen Dokumentationssystemen Deutschkenntnisse in Wort und Schrift, Englischkenntnisse unerlässlich Teamfähigkeit, vernetztes Denken und hohe Sozialkompetenz im Kontakt mit internen und externen Stellen Ihre Vorteile Das Kantonsspital Aarau führt eine eigene Tagesstätte für Kinder von Mitarbeitenden zwischen 0 und 12 [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
Max- Planck- Institut für Gesellschaftsforschung
Doctoral Positions in Economic Sociology and Political Economy
• Köln, NW Koeln
The Max Planck Institute for the
Study of Societies (MPIf G) offers graduate students an attractive
research environment at the International Max Planck Research School on the Social and Political [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Constitution of the Economy (IMPRS-SPCE) . Stellen Sie sicher, dass Sie die Informationen zu dieser Stelle gründlich lesen, bevor Sie sich bewerben. The IMPRS-SPCE is a joint Ph D program with the Faculty of Management, Economics [. .. ] disability, age, or sexual orientation or identity. xfuhyvp In diversity lies the basis for the cutting-edge research conducted at over 80 Max Planck Institutes. CONTACT Dr. Mischa Stratenwerth Academic Coordinator IMPRS-SPCE-254 Max Planck Institute for the Study of Societies Paulstraße 3 50676 Köln 79009510 [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Senior Clinical Trial Assistant
• Wiesbaden
Work-Life-Balance
[. .. ] protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate (CRA I) / Senior
• Wiesbaden
Work-Life-Balance
[. .. ] protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate I
• Wiesbaden
Work-Life-Balance
[. .. ] protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Manages the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas, with appropriate supervision. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and [. .. ] Current knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials is preferred Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Knowledge related to ICH/ GCP Guidelines and applicable local regulations is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, [. .. ]
Job vor 10 Tagen bei Jooble gefunden
Max Planck Institute for the History of Science
• Berlin
Abgeschlossene Ausbildung
Flexible Arbeitszeiten Betriebliche Altersvorsorge Jobticket 30+ Urlaubstage Tarifvertrag Work-Life-Balance
Skip to main content Institute Institute Founded in 1994, the Max Planck Institute for the History of Science (MPIWG) in Berlin is one of the more than 80
research [...]
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[...] institutes administered by the Max Planck Society. It is dedicated to the study of the history of science and aims to understand scientific thinking and practice as historical phenomena. People People The Max Planck Institute for the History of Science comprises scholars across all Departments and Research Groups, as well as an Administration team, IT Support, Library, Digital Humanities, and Research Communication and [. .. ]
Job vor 14 Tagen bei Jooble gefunden
Thermo Fisher Scientific
Clinical Trial Coordinator II (m/f/d) - Germany
• Karlsruhe
[. .. ] our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a [...]
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[...] step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes [. .. ] now and in the future. Location/ Division Specific Information Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants. Discover Impactful Work: PPD clinical research services mission is to improve health. It starts as an idea to cure. It becomes a life saved. All in-between, [. .. ]
Job am 18.01.2026 bei Jooble gefunden
Max- Planck- Institut für Gesellschaftsforschung
• Köln
Doctoral Positions in Economic Sociology and Political Economy The Max Planck Institute for the
Study of Societies ( MPIf G ) offers graduate students an attractive
research environment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] at the International Max Planck Research School on the Social and Political Constitution of the Economy ( IMPRS-SPCE ) . The IMPRS-SPCE is a joint Ph D program with the Faculty of Management, Economics and Social Sciences at the University of Cologne and the Faculty of Social Sciences [. .. ] belief, disability, age, or sexual orientation or identity. In diversity lies the basis for the cutting-edge research conducted at over 80 Max Planck Institutes. CONTACT Dr. Mischa Stratenwerth Academic Coordinator IMPRS-SPCE +49 221 2767254 Max Planck Institute for the Study of Societies Paulstraße 3 50676 Köln Doctoral Positions in Economic Sociology and Political Economy The Max Planck Institute for the Study of Societies ( MPIf G ) offers graduate students an attractive research environment at the International Max Planck Research [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Project Management Coordinator
• München
[. .. ] and initiative, where physical walls and different time zones dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of the Alira Health Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Milestone One
• München
Milestone One is a Site Enabling Organization with global headquarters in Zug, Switzerland. We understand what clinical
study sites need and our overall mission is to support sites in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] stronger study delivery. Job Description As Milestone One continues its global expansion, we are seeking an experienced Operations Manager to join our international team. This newly created role is critical to ensuring operational excellence across our regional activities and supporting the scalable, high-quality delivery of clinical research projects worldwide. The Operations Manager will take full operational ownership of assigned regions, leading site operations, managing coordinator teams, and ensuring that clinical trials are executed efficiently, compliantly, and without disruption. This role requires a hands-on leader with deep knowledge of clinical trial operations who can proactively identify and resolve day-to-day challenges in a dynamic international environment. This is a regional role, with the region [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Milestone One
Area Operations Manager-Clinical
• München
Milestone One is a Site Enabling Organization with global headquarters in Zug, Switzerland. We understand what clinical
study sites need and our overall mission is to support sites in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] stronger study delivery. As Milestone One continues its global expansion, we are seeking an experienced Operations Manager to join our international team. This newly created role is critical to ensuring operational excellence across our regional activities and supporting the scalable, high-quality delivery of clinical research projects worldwide. The Operations Manager will take full operational ownership of assigned regions, leading site operations, managing coordinator teams, and ensuring that clinical trials are executed efficiently, compliantly, and without disruption. This role requires a hands-on leader with deep knowledge of clinical trial operations who can proactively identify and resolve day-to-day challenges in a dynamic international environment. Take end-to-end operational responsibility for clinical [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Marriott International
• Berlin
[. .. ] involve cross-functional team collaboration, stakeholder communication, and the development of strong project and time management skills essential for future success. The internship must be a compulsory part [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of the study program TASKS RESPONSIBILITIES As a Digital Marketing Intern, you will support the day-to-day execution and optimization of our digital marketing efforts. Digital Content Creation Website Management Implement new hotel profiles, promotions, editorial content, event RSVP pages, and more, on Review, coordinate assets, and upload updates on existing website [. .. ] experience with key digital tools including: CMS (Content Management System) CRM (Customer Relationship Management) Google Analytics Google Ads Asana Identify trends and improvement opportunities and collaborate with the Digital Marketing Coordinator to optimize performance Creating Keynote reports on digital marketing communication performance, for both internal and external stakeholders Research Department Support Conduct market and competitor research to support digital strategies and content decisions Provide general administrative assistance and contribute to departmental projects as they arise during the internship Strong affinity for marketing or digital marketing Excellent English written and verbal communication skills-German is not required Excellent organizational and [. .. ]
Job am 21.01.2026 bei JobMESH gefunden
Max- Planck- Institut für Gesellschaftsforschung
Doctoral Positions in Economic Sociology and Political Economy
• North Rhine- Westphalia Cologne
The Max Planck Institute for the
Study of Societies (MPIf G) offers graduate students an attractive
research environment at the International Max Planck Research School on the Social [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Political Constitution of the Economy (IMPRS-SPCE) . The IMPRS-SPCE is a joint Ph D program with the Faculty of Management, Economics and Social Sciences at the University of Cologne and the Faculty of Social Sciences at the [. .. ] belief, disability, age, or sexual orientation or identity. In diversity lies the basis for the cutting-edge research conducted at over 80 Max Planck Institutes. CONTACT Dr. Mischa Stratenwerth Academic Coordinator IMPRS-SPCE-254 Max Planck Institute for the Study of Societies Paulstraße 3 50676 Köln DUBLETTEOVERRIDE 76981832 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
• Homeoffice
Work-Life-Balance
ICON plc is a world-leading healthcare intelligence and clinical
research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on our mission to shape the future of clinical development. As a Site Engagement Liaison (SEL) will be responsible for developing relationships with clinical trial investigators and research site staff to [. .. ] this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally. What you will be doing: Work with clinical research associates (CRAs) and the study team to ensure that investigators and site staff have a thorough understanding of the investigational agents being used in the study, the trials eligibility criteria, and all study procedures Responsible for site start-up and activation, for study conduct and close-out and being local expert by providing site recommendations [. .. ] are: Experience in site management, start-up activities to site activation, and close-out activities Exposure to the clinical research environment as a SEL, medical science liaison (MSL) , study coordinator, Senior CRA or experience in a CRO Demonstrated knowledge of quality and regulatory requirements in applicable countries Excellent communication skills in German and English Ability to travel What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
Clinical Research Coordinator/ Study Nurse (m/w/d) - Neuwied
• Koblenz
Sind Sie auf der Suche nach einer neuen Chance oder Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht derzeit einen Clinical
Research Coordinator/
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>Study Nurse (m/w/d) zur Unterstützung der Durchführung einer klinischen Studie an einem Zentrum in Neuwied. Diese Position ist ab sofort zu besetzen, zunächst befristet auf 6 Monate. Der Umfang beträgt 24 Stunden pro Woche. Zu den täglichen Aufgaben gehören: Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den [. .. ]
▶ Zur Stellenanzeige
Job am 14.01.2026 bei Jooble gefunden
IQVIA
• Münster
Teilzeit
Sind Sie auf der Suche nach einer Chance oder einer neuen Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht eine/n engagierte/ n
Study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Nurse/ Clinical Research Coordinator (m/w/d) zur Unterstützung einer klinischen Studie am Standort in Münster. Diese Teilzeitstelle (24 Stunden pro Woche) mit Start per sofort ist zunächst bis zum 30.08.20 26 zu besetzen. Zu den täglichen Aufgaben gehören: Koordination und Organisation klinischer Studienabläufe Sicherstellung eines sicheren Studienumfelds gemäß Gesundheits- und Sicherheitsrichtlinien [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
Study Nurse (m/w/d)
• Mannheim
Homeoffice möglich
[. .. ] unerwünschten Ereignissen und Produktbeschwerden gemäß den geltenden Anforderungen verantwortlich. Das bringen Sie mit: Examinierte Krankheits- und Gesundheitspfleger/-in oder eine gleichwertige Ausbildung mit mindestens 1 Jahr Berufserfahrung Erfahrung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in Studien (Study Nurse/ Study Coordinator) Sehr gutes Verständnis und allgemeine Kenntnisse des Gesundheitswesens Flexibilität (neue Projekte, Arbeitszeit) Sie organisieren Ihren Arbeitsalltag gerne eigenverantwortlich Sie sind ein echter Teamplayer und pflegen gerne nachhaltige Beziehungen zu ihren Ansprechpartnern Das bieten wir Ihnen: Ein attraktives Gehaltspaket Firmen PKW auch zur Privatnutzung (ohne Zuzahlung) Moderne IT-Ausstattung Attraktive Sozialleistungen [. .. ] per Mail an: click to reveal email address #LI-CES #LI-DNP #LI-SS2 #Nurses #Field Nurse IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at 76125238 [. .. ]
Job am 23.01.2026 bei Stellen-Online.de gefunden
Max- Planck- Institut für Gesellschaftsforschung
Doctoral Positions in Economic Sociology and Political Economy-Vollzeit
• Köln, 50678, 50667
The Max Planck Institute for the
Study of Societies (MPIf G) offers graduate students an attractive
research environment at the International Max Planck Research School on the Social [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Political Constitution of the Economy (IMPRS-SPCE) . The IMPRS-SPCE is a joint Ph D program with the Faculty of Management, Economics and Social Sciences at the University of Cologne and the Faculty of Social Sciences at the [. .. ] belief, disability, age, or sexual orientation or identity. In diversity lies the basis for the cutting-edge research conducted at over 80 Max Planck Institutes. CONTACT Dr. Mischa Stratenwerth Academic Coordinator IMPRS-SPCE +49 221 2767-254 Max Planck Institute for the Study of Societies Paulstraße 3 50676 Köln Soziologie Doktorand, Doktorandin Lehre Forschung, Wissenschaft Forschungseinrichtung Vollzeit-gefunden bei stellenonline. de 77545929 [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Complexity Science Hub
Visiting Researcher
• AT- 9 Wien
WE SEARCH FOR The Visiting Researcher Program invites graduate students, postdocs, and established researchers to join the
research community at the Complexity Science Hub in order to enhance their [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] research. Visiting Researchers use their affiliation with CSH to either: extend their ongoing research using knowledge, methods, tools, or data specific to CSH; or undertake a new project that is closely aligned with CSH research themes. In exchange, Visiting [. .. ] us; and (iv) the desired length of the research stay and, if known, preferred dates. Additional documents For graduate students and postdoctoral fellows: Brief letter of support from the supervisor, study director, or program chair/ coordinator. This is not a letter of recommendation but rather should simply specify that, if accepted, the researcher would be eligible to undertake a research visit at CSH. For Masters students: Unofficial transcript or list of relevant coursework. J-18808-Ljbffr 78527361 [. .. ]
Neu Job vor 6 Std. bei Jobleads gefunden
One or two Start-up Grants of the Doctoral Program in Literary Studies (32, 000 Swiss francs each)
• Basel, Basel- Stadt
[. .. ] the University of Basel offers doctoral students excellent conditions for writing their dissertations in literary studies and closely related fields. Selected seminars, regular doctoral colloquia, as well [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as retreats and study days provide opportunities to exchange ideas, receive feedback on work in progress, and acquire skills for an academic career. The Program also supports members with contributions to conferences, research trips, archival travel and financial support for their own events. The Start-Up Grant The one-year start-up grant (application deadline: April 12, 2026; start date: October 1, 2026) is intended to contribute to living expenses during the elaboration phase of a dissertation project in literary studies. The aim [. .. ] must present a confirmation of supervision no later than the interview. Read our website carefully. The following documents should be sent in electronic form (collected in one PDF) to the coordinator of the Doctoral Program in Literary Studies: by April 12, 2026: letter of motivation curriculum vitae (with list of publications, if applicable) outline of the dissertation project (max. 5 pages plus bibliography) degree certificate with final grade (MA degree or equivalent; if the certificate is not yet available, include a [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical Research Associate-Pathology
• Mannheim, Baden- Württemberg
Ready to be the heartbeat of medical
research? Join our client as a
Study Coordinator and assist in turning innovative science into life-changing care R D Partners is seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Clinical Research Associate to support the planning, coordination, and execution of clinical research studies. You will work closely with study sites to ensure compliance with protocols, regulations, and best practices. This role involves collaboration [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Clinical Research Associate III (m/f/d)
• Stein, Baden- Württemberg
[. .. ] As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together. We are [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] hiring a Clinical Research Associate III (m/f/d) Location: EMEA (Flexible) . Your Strength Minimum of 4 years of advanced experience in clinical research monitoring In-depth knowledge of regulations and guidelines related to clinical trials on human subjects (e. g. , ISO 14155, GCP, MDR, EU, FDA) Ability to manage 1015 study sites independently, from start-up to closure Excellent communication skills for site interaction, training, and issue resolution Strong collaboration and mentorship abilities CRA IIIs are expected to guide junior team members Handson experience with monitoring systems, data verification, and compliance tracking Strong organizational skills and the ability to manage multiple [. .. ] safety and protocol adherence Conduct site training, initiate visits, and support audit/ inspection readiness Collaborate with other departments such as Data Management, Clinical Operations, and Medical Affairs Support investigator and coordinator meetings, and provide training or presentations as needed Mentor junior CRAs and contribute to continuous process improvement Participate in CAPA execution, audits, and ongoing quality assurance activities Our Strength A purpose-driven Clinical Affairs team committed to quality and patient safety Onboarding and development in a structured, supportive environment Exposure [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Research Study Coordinator pro Jahr?
Als Research Study Coordinator verdient man zwischen EUR 45.000,- bis EUR 65.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Research Study Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 54 offene Stellenanzeigen für Research Study Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Research Study Coordinator Jobs?
Aktuell suchen 20 Unternehmen nach Bewerbern für Research Study Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Research Study Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Research Study Coordinator Stellenangebote:
- Abb Vie (6 Jobs)
- IQVIA (6 Jobs)
- Milestone One (3 Jobs)
- Georgetown University in Qatar (3 Jobs)
- Thermo Fisher Scientific (2 Jobs)
In welchen Bundesländern werden die meisten Research Study Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Research Study Coordinator Jobs werden derzeit in Bayern (8 Jobs), Nordrhein-Westfalen (7 Jobs) und Baden-Württemberg (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Research Study Coordinator Jobs?
Research Study Coordinator Jobs gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.
