14 Jobs für Clinical Study Assistant
Stellenangebote Clinical Study Assistant Jobs
Job vor 6 Tagen bei Jobleads gefunden
• München, Bayern
[. .. ] active participant in the local study team (s) . The CRA works in close collaboration with local team members (Project Management Clinical Operations (PMCO) , Study Start-Up [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (SSU) manager, Clinical Study Assistant (CSA) and other CRAs in Clinical Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner on a site level. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure delivery and [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description Acts as primary communication point for project teams and company [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] departments regarding clinical data management. Acts as primary communication point for clients/ vendors for all data management aspects of clinical projects and clinical data management reporting. Responsible for the supervision of all project data management activities of assigned studies. Coordinates data management activities within clinical projects including but not limited to EDC development, [. .. ] generation of final Data Management deliverables. Provides input into monitoring of project scope, budget, timelines, and deliverables. Responsible for clinical data management activities including, but not limited to: development of study documentation, User acceptance testing, User access management, Data review, e CRf/External data reconciliation, SAE reconciliation, Query management, Study Database Lock activities, Archival of CRFs QC coordination, Project status reporting, Data listings/ Patient profiles generation and delivery Maintains and QCs e TMF. Maintains and QCs Data Management working files. Participates in preparation [. .. ] and client/ third-party audits/ inspections of Data Management. Participates in follow-up on and resolution of audit findings pertaining to Data Management. Trains Lead Data Managers, Data Managers and Assistant Data Managers. Conducts project-specific training of the clinical team in CRF completion and presents at the Investigator Meetings. Provides input into proposals and assists with Business Development activities. Participates in process improvement activities at corporate/ departmental level. Qualifications College or University degree or equivalent combination of training and experience [. .. ]
Job am 28.01.2026 bei Jobleads gefunden
• Berlin
Overview WHITE MOUNTAINS COMMUNITY COLLEGE NURSING FACULTY (INSTRUCTOR/
ASSISTANT PROFESSOR/ ASSOCIATE PROFESSOR/ PROFESSOR) Annual Salary (determined by faculty level to which assigned) : INSTRUCTOR LEVEL: 49, 383 57, 639 ASSISTANT [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] PROFESSOR LEVEL: 53, 265 62, 374 ASSOCIATE PROFESSOR LEVEL: 57, 639 67, 546 PROFESSOR LEVEL: 65, 207 77, 041 INSTRUCTOR LEVEL SCOPE OF WORK : To educate students in [. .. ] Complies with all college, system, state and federal rules and regulations. Other duties as assigned. MINIMUM QUALIFICATIONS Education: Masters degree from a regionally accredited college or university with a major study in the field of nursing. Experience: Two years of teaching experience in nursing, or two years of experience directly related to the field of nursing. License/ Certification: Must possess current or active Registered Nurse license in New Hampshire. Must meet the continuing education requirements by the Board of Nursing to [. .. ] college appointing authority. DISCLAIMER STATEMENT: These class specifications are descriptive of general duties and are not intended to list every specific function of these class titles. Position requires travel to clinical site locations. To be considered for this position, please complete the online application at https:/ / . For more information, please contact WMCC is an equal opportunity employer and does not discriminate on the basis of race, creed, color, religion, ancestry or national origin, age, sex, sexual orientation, gender identity [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
• München, Bayern
Regulatory And
Clinical Start Up Specialist (Biotech) Join to apply for the Regulatory And Clinical Start Up Specialist (Biotech) role at Progressive Direct message the job poster from Progressive Regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Start up Associate/ Specialist Responsible for oversight of assigned global clinical trials Review of regulatory submission documents and packages Support study teams as RA representative Preparation of responses to regulatory requests Support of regulatory interactions as applicable Negotiation of Budgets Contract Management Experience Requirements University degree or professional education e. g. Pharmaceutical/ Medical Technical Assistant with a minimum of 1-2 years professional experience preferably in pharmaceutical industry (an academic degree in natural sciences e. g. Bachelor would be an advantage) Fluent in written and verbal English Advanced knowledge and on-hands experience in using office software-e. g. MS Office Programs, SAP, Zoom, Teams [. .. ]
Job vor 11 Tagen bei Neuvoo gefunden
PSI
• Kassel, Hessen
Job Description The Milestone One Site Coordinator role supports a
Clinical Study Site in clinical trial related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] goals. The function of the role may include, but not limited to, any/ all of the following: Actas the main line of communication between the Sponsor or CRO and the site. [. .. ] and delegation of responsibilities. Preparefor and participatein onsite study audits or regulatory agency inspections. Qualifications Completed vocational training as a nurse (Gesundheits- und Krankenpfleger/in or Pflegefachfrau/ Pflegefachmann) or Medical Assistant (MFA Medizinische Fachangestellte) , or completed degree in a relevant field (e. g. health sciences, biology, pharmacy, public health) Minimum of 2 years of on-the-job experience as a site coordinator Ability to work in a fast-paced environment, with short timelines and multiple tasks to be completed simultaneously. [. .. ]
Job vor 12 Tagen bei Neuvoo gefunden
Milestone One
• Kassel, Hesse
Job Description The Milestone One Site Coordinator role supports a
Clinical Study Site in clinical trial related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] goals. The function of the role may include, but not limited to, any/ all of the following: Act as the main line of communication between the Sponsor or CRO and the [. .. ] of responsibilities. Prepare for and participate in onsite study audits or regulatory agency inspections. Qualifications Completed vocational training as a nurse (Gesundheits- und Krankenpfleger/in or Pflegefachfrau/ Pflegefachmann) or Medical Assistant (MFA Medizinische Fachangestellte) , or completed degree in a relevant field (e. g. health sciences, biology, pharmacy, public health) Minimum of 2 years of on-the-job experience as a site coordinator Ability to work in a fast-paced environment, with short timelines and multiple tasks to be completed simultaneously. [. .. ]
Job vor 13 Tagen bei Neuvoo gefunden
IQVIA
• Frankfurt, Hessen
Homeoffice möglich
The IQVIA sponsor-dedicated
Clinical Functional Service Partnerships (Clinical FSP) department issupporting our clients project team in the execution of clinical trials. Joining the team provides the opportunity to work with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the preparation and documentation of clinical research projects in different therapeutic areas in Germany or the DACH region. You will be involved in data management, creation of study related documents and correspondence with internal departments, research sites and our client to ensure a complete and accurate Trial Master File delivery. We currently offer an exciting opportunity to join the team as Experienced Clinical Trial Coordinator (m/w/d) to work in home-office within the Ulm/Biberach an [. .. ] or pharmaceutical field or within office management. At least 2-4 years experience as Clinical Trial Coordinator or within another administrative role in clinical research, e. g. as Clinical Trials Assistant, Study Start-Up Assistant. Knowledge of applicable clinical research regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Fluent languages skills in German on at least C1 level and good command of English. Computer skills including working knowledge of Microsoft Word, Excel and [. .. ]
Job am 05.03.2026 bei Neuvoo gefunden
PSI CRO
Principal Lead Data Manager
• Munich, Bavaria
Führungs-/ Leitungspositionen
Job Description Acts as primary communication point for project teams and company departments regarding
clinical data management. Acts as primary communication point for clients/ vendors for all data management aspects [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of clinical projects and clinical data management reporting. Responsible for the supervision of all project data management activities of assigned studies. Coordinates data management activities within clinical projects including but not limited to EDC development, [. .. ] generation of final Data Management deliverables. Provides input into monitoring of project scope, budget, timelines, and deliverables. Responsible for clinical data management activities including, but not limited to: development of study documentation, User acceptance testing, User access management, Data review, e CRf/External data reconciliation, SAE reconciliation, Query management, Study Database Lock activities, Archival of CRFs QC coordination, Project status reporting, Data listings/ Patient profiles generation and delivery Maintains and QCs e TMF. Maintains and QCs Data Management working files. Participates in preparation [. .. ] and client/ third-party audits/ inspections of Data Management. Participates in follow-up on and resolution of audit findings pertaining to Data Management. Trains Lead Data Managers, Data Managers and Assistant Data Managers. Conducts project-specific training of the clinical team in CRF completion and presents at the Investigator Meetings. Provides input into proposals and assists with Business Development activities. Participates in process improvement activities at corporate/ departmental level. Qualifications College or University degree or equivalent combination of training and experience [. .. ]
Job am 22.02.2026 bei Neuvoo gefunden
ICON
• Frankfurt, Hessen
Work-Life-Balance
Clinical Research Lead
Assistant 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Clinical Trial Assistant (CTA) [. .. ] Doing: Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records. Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements. Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study. Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials. Building and maintaining strong relationships with site staff and [. .. ]
Job am 15.02.2026 bei Neuvoo gefunden
Fraunhofer- Gesellschaft
• Leipzig, Saxony
Werkstudenten
[. .. ] professional home for scientists, engineers, laboratory technicians, and administrative staff who work together in the service of health. Are you looking for an opportunity to work as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a student research assistant during your studies? Then youve come to the right place At Fraunhofer IZI, we regularly mentor committed talents who want to conduct cutting-edge research with us. Be part of change At our institute, our employees delve into exciting projects and develop individual products and services for our clients, primarily [. .. ] range of treatments in the future and give patients new hope. Together with our partners, we at the Fraunhofer IZI are driving forward the implementation of these pioneering approaches in clinical practice. Infectious diseases pose a constant challenge to global health-for humans and animals. To counteract these threats, we at Fraunhofer IZI are researching the mechanisms of disease transmission and development as well as innovative diagnostic and therapeutic approaches. Our infectious disease pathology team works closely with international partners to [. .. ] You can find an overview of our business areas and departments. What you contribute You are an enrolled student, preferably in life sciences, engineering, medicine or a related field of study. Ideally, you have already gained some experience through internships, vacation jobs or working student positions in the field you are interested in, but this is not a must. In any case, please always include a short cover letter with your application in which you explain your motivation for working as [. .. ]
Job am 15.02.2026 bei Neuvoo gefunden
Thermo Fisher Scientific
Assistant CRA (m/f/d) (Open)
• Karlsruhe, Baden- Württemberg
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
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[...] 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 that people and communities depend on now and in [. .. ] power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. Discover Impactful Work: As an Assistant CRA, you will perform remote site management and monitoring activities on assigned project (s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and company procedural documents by reviewing study data from various sources remotely. You will contact study sites to collect study documentation, resolve issues and request outstanding information. A day in the Life: Develops and maintains a close and collaborative communication with the site staff. Actively discusses protocol conduction, enrollment rates and strategies, open issues, EDC completion and [. .. ]
Job am 18.01.2026 bei Neuvoo gefunden
PSI
Principal Lead Data Manager.
• Munich, Bavaria
Führungs-/ Leitungspositionen
Job Description Acts as primary communication point for project teams and company departments regarding
clinical data management. Acts as primary communication point for clients/ vendors for all data management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] aspects of clinical projects and clinical data management reporting. Responsible for the supervision of all project data management activities of assigned studies. Coordinates data management activities within clinical projects including but not limited to EDC development, [. .. ] generation of final Data Management deliverables. Provides input into monitoring of project scope, budget, timelines, and deliverables. Responsible for clinical data management activities including, but not limited to: development of study documentation, User acceptance testing, User access management, Data review, e CRf/External data reconciliation, SAE reconciliation, Query management, Study Database Lock activities, Archival of CRFs QC coordination, Project status reporting, Data listings/ Patient profiles generation and delivery Maintains and QCs e TMF. Maintains and QCs Data Management working files. Participates in preparation [. .. ] and client/ third-party audits/ inspections of Data Management. Participates in follow-up on and resolution of audit findings pertaining to Data Management. Trains Lead Data Managers, Data Managers and Assistant Data Managers. Conducts project-specific training of the clinical team in CRF completion and presents at the Investigator Meetings. Provides input into proposals and assists with Business Development activities. Participates in process improvement activities at corporate/ departmental level. Qualifications College or University degree or equivalent combination of training and experience [. .. ]
Job am 16.12.2025 bei Neuvoo gefunden
Hays
Clinical Trial Assistant (m/w/d)
• Dresden, Saxony
Angebote von Zeitarbeitsunternehmen
Clinical Trial
Assistant (m/w/d) Festanstellung durch unseren Kunden Dresden Startdatum: sofort Referenznummer: 823445/ 1 Diesen Job teilen oder drucken Aufgaben Erarbeitung, Bearbeitung, Pflege und Verfolgung studienspezifischer Dokumente sowie [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] notwendiger Genehmigungsunterlagen inkl. Prozessbegleitung und Aktualisierung (Phase Ib bis IV, NIS, Register, MDR) bei Behörden und Institutionen Ansprechpartner für Prüfärzte, Studiensekretariate und Auftraggeber [. .. ] Mitwirkung bei der Erstellung und Weiterentwicklung standardisierter Arbeitsanweisungen (SOPs) und sicherheitsrelevanter Dokumente Profil Medizinische Dokumentationsassistenz/ Studium der Naturwissenschaften/ CRA/ Fachangestellte für Medien- und Informationsdienste oder einem Gesundheitsberuf (Gesundheits- und Krankenpfleger, Study Nurse, MTA, PTA oder MFA) GCP Zertifikat und Kenntnisse von medizinischen Grundbegriffen Erfahrungen bei der Organisation von klinischen Studien wünschenswert Sehr gute Kommunikationsfähigkeiten, Flexibilität, organisatorisches Geschick und die Bereitschaft zur Teamarbeit Kenntnisse in der Med DRA Kodierung sind von Vorteil Sehr gute Kenntnisse der deutschen und englischen Sprache in Wort und [. .. ]
Job am 07.11.2025 bei Neuvoo gefunden
Alcedis GmbH
Projektassistenz im Bereich klinische Studien/ Project Assistant Clinical Operations (m/w/d) , Projektassistenz im Bereich klinische Studien/ Project Assistant Clinical Operations (m/w/d) bei Alce
• Giessen, Hessen
Homeoffice möglich Abgeschlossene Ausbildung
Flexible Arbeitszeiten 30+ Urlaubstage
Projektassistenz im Bereich klinische Studien/ Project
Assistant Clinical Operations (m/w/d) bei Alcedis Gmb H softgarden View job here Projektassistenz im Bereich klinische Studien/ Project Assistant Clinical Operations (m/w/d) Vollzeit Hybrid [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Gießen, Deutschland Ohne Berufserfahrung 06.02.26 Als Projektassistenz (m/w/d) unterstützt du unsere Fachabteilung Clinical Operations auf vielfältige Weise bei der Durchführung und [. .. ] Durchführbarkeitsprüfung (Feasibility) für neue Projekte mit Prüfzentren Unterstützung bei der Erstellung von Studienunterlagen inkl. Versand und Tracking Vorbereitung von Unterlagen zur Einreichung bei Behörden und Ethikkommissionen Erstellung und Verwaltung der Study Master File Unterstützung der Zentren bei der Bearbeitung von Rückfragen zu den elektronischen erfassten Studiendaten Korrespondenz (nach Vorlage oder eigenem Konzept in Deutsch und Englisch) Versand und Tracking von Dokumenten und Studienmaterial an Prüfzentren Erstellung/ Bearbeitung von Studienverträgen (nach Vorgabe) Vorbereitung von Unterlagen für die Honorierung der Prüfzentren Organisation von [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Study Assistant pro Jahr?
Als Clinical Study Assistant verdient man zwischen EUR 35.000,- bis EUR 55.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Study Assistant Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 14 offene Stellenanzeigen für Clinical Study Assistant Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Study Assistant Jobs?
Aktuell suchen 10 Unternehmen nach Bewerbern für Clinical Study Assistant Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Study Assistant Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Study Assistant Stellenangebote:
- PSI (2 Jobs)
- Milestone One (1 Job)
- IQVIA (1 Job)
- PSI CRO (1 Job)
- ICON (1 Job)
- Fraunhofer- Gesellschaft (1 Job)
In welchen Bundesländern werden die meisten Clinical Study Assistant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Study Assistant Jobs werden derzeit in Hessen (5 Jobs), Sachsen-Anhalt (4 Jobs) und Bayern (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Study Assistant Jobs?
Clinical Study Assistant Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
