Aktuelle Jobs im Zusammenhang mit Clinical Trial Associate - Monheim am Rhein - TN Germany


  • Frankfurt am Main, Hessen, Deutschland Pharmiweb Vollzeit

    Job SummaryWe are seeking a highly skilled Freelance Clinical Research Associate to join our team at ClinChoice. As a key member of our clinical operations team, you will be responsible for ensuring the successful execution of clinical trials across various therapeutic areas.Key ResponsibilitiesConduct site initiation visits, monitor study progress, and...


  • Frankfurt am Main, Hessen, Deutschland Pharmiweb Vollzeit

    Unlock Your Potential as a Clinical Research AssociateAre you passionate about advancing medical treatments and improving patient outcomes? Do you have a strong foundation in life sciences and a desire to work in a dynamic, fast-paced environment? If so, we invite you to explore the exciting opportunity of a Clinical Research Associate role at Pharmiweb.As a...


  • Frankfurt am Main, Hessen, Deutschland Pharmiweb Vollzeit

    Unlock Your Potential as a Clinical Research AssociateAre you passionate about advancing medical treatments and improving patient outcomes? Do you have a strong foundation in life sciences and a desire to work in a dynamic, fast-paced environment? If so, we invite you to explore the exciting opportunity of a Clinical Research Associate role at Pharmiweb.As a...

  • Clinical Trial Manager

    vor 4 Wochen


    Frankfurt am Main, Hessen, Deutschland IQVIA Vollzeit

    Job Title: Clinical Trial ManagerIQVIA is seeking a highly skilled Clinical Trial Manager to join our team in Germany. As a Clinical Trial Manager, you will be responsible for managing clinical research projects in different therapeutic areas, working closely with our client's project team to ensure successful trial execution.Responsibilities:Manage clinical...

  • Clinical Trial Manager

    vor 4 Wochen


    Frankfurt am Main, Hessen, Deutschland IQVIA Vollzeit

    Job Title: Clinical Trial ManagerIQVIA is seeking a highly skilled Clinical Trial Manager to join our team in Germany. As a Clinical Trial Manager, you will be responsible for managing clinical research projects in different therapeutic areas, working closely with our client's project team to ensure successful trial execution.Responsibilities:Manage clinical...

  • Clinical Trial Manager

    vor 3 Wochen


    Frankfurt am Main, Hessen, Deutschland IQVIA Vollzeit

    Job Title: Clinical Trial ManagerIQVIA is seeking a highly skilled Clinical Trial Manager to join our team in Germany. As a Clinical Trial Manager, you will be responsible for managing clinical research projects in different therapeutic areas, working closely with our client's project team to ensure successful trial execution.Responsibilities:Manage clinical...

  • Clinical Trial Manager

    vor 3 Wochen


    Frankfurt am Main, Hessen, Deutschland IQVIA Vollzeit

    Job Title: Clinical Trial ManagerIQVIA is seeking a highly skilled Clinical Trial Manager to join our team in Germany. As a Clinical Trial Manager, you will be responsible for managing clinical research projects in different therapeutic areas, working closely with our client's project team to ensure successful trial execution.Responsibilities:Manage clinical...

  • Clinical Trial Manager

    vor 4 Wochen


    Frankfurt am Main, Hessen, Deutschland Pharmiweb Vollzeit

    Job Title: Clinical Trial ManagerWe are seeking a highly skilled Clinical Trial Manager to join our team in Germany. As a Clinical Trial Manager, you will be responsible for the operational management of clinical trials, ensuring compliance with regulatory requirements and client SOPs.Key Responsibilities:Manage the execution of clinical studies, including...

  • Clinical Trial Manager

    vor 4 Wochen


    Frankfurt am Main, Hessen, Deutschland Pharmiweb Vollzeit

    Job Title: Clinical Trial ManagerWe are seeking a highly skilled Clinical Trial Manager to join our team in Germany. As a Clinical Trial Manager, you will be responsible for the operational management of clinical trials, ensuring compliance with regulatory requirements and client SOPs.Key Responsibilities:Manage the execution of clinical studies, including...


  • Ingelheim am Rhein, Rheinland-Pfalz, Deutschland Georgetown University in Qatar Vollzeit

    Job SummaryWe are seeking a highly skilled Clinical Research Nurse I to join our team at Georgetown University in Qatar. The successful candidate will be responsible for coordinating and managing clinical trials in oncology, ensuring the highest level of patient care and research integrity.Key ResponsibilitiesManage the overall coordination of assigned...


  • Ingelheim am Rhein, Rheinland-Pfalz, Deutschland Georgetown University in Qatar Vollzeit

    Job SummaryWe are seeking a highly skilled Clinical Research Nurse I to join our team at Georgetown University in Qatar. The successful candidate will be responsible for coordinating and managing clinical trials in oncology, ensuring the highest level of patient care and research integrity.Key ResponsibilitiesManage the overall coordination of assigned...


  • Frankfurt am Main, Hessen, Deutschland Pharmiweb Vollzeit

    Main Job Tasks and Responsibilities:Stay up-to-date with scientific, regulatory, and operational aspects relevant to assigned clinical projects.Assist in site selection, evaluation visits, initiation visits, and ensure follow-up by obtaining pre-study documentation for smooth site start-up.May act as Feasibility Associate after documented training.Train site...


  • Ingelheim am Rhein, Rheinland-Pfalz, Deutschland Georgetown University in Qatar Vollzeit

    Job SummaryThe Clinical Research Coordinator I serves as a key member of the research team at Georgetown University, responsible for the coordination and management of oncology clinical trials. This role requires strong organizational and communication skills, as well as the ability to work independently and as part of a team.Key ResponsibilitiesCoordinate...


  • Ingelheim am Rhein, Rheinland-Pfalz, Deutschland Georgetown University in Qatar Vollzeit

    Job SummaryThe Clinical Research Coordinator I serves as a key member of the research team at Georgetown University, responsible for the coordination and management of oncology clinical trials. This role requires strong organizational and communication skills, as well as the ability to work independently and as part of a team.Key ResponsibilitiesCoordinate...

  • Research Coordinator

    vor 2 Monaten


    Ingelheim am Rhein, Rheinland-Pfalz, Deutschland Georgetown University in Qatar Vollzeit

    Job SummaryWe are seeking a highly motivated and detail-oriented Clinical Research Coordinator I to join our team at Georgetown University in Qatar. The successful candidate will be responsible for coordinating and managing clinical trials in oncology, ensuring compliance with regulatory requirements and institutional policies.Key ResponsibilitiesCoordinate...

  • Research Coordinator

    vor 4 Wochen


    Ingelheim am Rhein, Rheinland-Pfalz, Deutschland Georgetown University in Qatar Vollzeit

    Job SummaryWe are seeking a highly motivated and detail-oriented Clinical Research Coordinator I to join our team at Georgetown University in Qatar. The successful candidate will be responsible for coordinating and managing clinical trials in oncology, ensuring compliance with regulatory requirements and institutional policies.Key ResponsibilitiesCoordinate...


  • Frankfurt am Main, Deutschland Warman O'Brien Vollzeit

    **Clinical Research Associate - World Leading CRO - Permanent** We are seeking an experienced Clinical Research Associate to take on an exciting opportunity with an international CRO that is continuing to lead from the front in the industry. Utilising their unique experience and global reach, this CRO has regularly demonstrated why they are market leaders...


  • Ingelheim am Rhein, Rheinland-Pfalz, Deutschland Georgetown University in Qatar Vollzeit

    Job SummaryThe Clinical Research Coordinator I serves as a key member of the research team at Georgetown University, responsible for the coordination and management of oncology clinical trials. This role requires strong organizational and communication skills, as well as the ability to work independently and as part of a team.Key ResponsibilitiesCoordinate...


  • Ingelheim am Rhein, Rheinland-Pfalz, Deutschland Georgetown University in Qatar Vollzeit

    Job SummaryThe Clinical Research Coordinator I serves as a key member of the research team at Georgetown University, responsible for the coordination and management of oncology clinical trials. This role requires strong organizational and communication skills, as well as the ability to work independently and as part of a team.Key ResponsibilitiesCoordinate...


  • Frankfurt am Main, Deutschland Novasyte Vollzeit

    The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved in data...

Clinical Trial Associate

vor 2 Monaten


Monheim am Rhein, Deutschland TN Germany Remote-Arbeit Freiberufler Vollzeit

Clinical Trial Associate (m/w/d) Anstellung bei der Hays Professional Solutions GmbH Monheim Startdatum: sofort Referenznummer: 774824/1 Diesen Job teilen oder drucken Aufgaben Entwicklung eines Trial Master File (TMF) Plans, Durchführung laufender und abschließender Qualitätskontrollen (QC) des TMF für Abschnitte, die dem Clinical Project Manager (CPM) gehören Versorgung der Clinical Research Organisation (CRO) oder des Partners mit Rückfragen/Feedback, um die Richtigkeit und Vollständigkeit der Dokumente und des TMF insgesamt sicherzustellen Unterstützung des Program Delivery Lead (PDL)/CPM bei der Einrichtung von Studien im Clinical Trial Management System (CTMS) Bereitstellung von Informationen für das CTMS-Team Durchführung laufender und abschließender Qualitätskontrollen des CTMS Verbindung zwischen Partnern, CPM, Studienärzten, Clinical Development Quality (CDQ) und der Rechtsabteilung Beantragung der Einrichtung von Studienpostfächern für alle Studien und Sicherstellung der Zugangsverwaltung Zusammenarbeit mit CPM Unterstützung von Audit-/Inspektionsaktivitäten und Unterstützung des Clinical Development Quality Lead (CDQL) Teilnahme an Sitzungen des klinischen Studienteams und/oder anderen prüfungsbezogenen Sitzungen Profil Ein abgeschlossener naturwissenschaftlicher Hochschulabschluss  Berufserfahrung in einem Arbeitsumfeld der klinischen Entwicklung  Gute Englischkenntnisse in Wort und Schrift Kenntnisse der Guten Klinischen Praxis (GCP) und der Richtlinien des Internationalen Rates für die Harmonisierung der technischen Anforderungen an Humanarzneimittel (ICH), der Food and Drug Administration (FDA) und/oder der Vorschriften der Europäischen Union (EU) Ausgezeichnete Kommunikationsfähigkeiten und Liebe zum Detail Sehr gute Kenntnisse der Microsoft Office Suite Benefits Betreuung im gesamten Bewerbungsprozess Betreuung im laufenden Projekt durch unser Team