133 Jobs für Clinical Research Associate
Stellenangebote Clinical Research Associate Jobs
Job vor 3 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Flexible Arbeitszeiten Work-Life-Balance
[. .. ] Kompetenzen und deiner Leidenschaft maßgeblich dazu bei, medizinische Entwicklungen nach vorn zu bringen. Stell dein Know-how unter Beweis und werde Teil unseres eignen klinischen Forschungsteams in Wiesbaden [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] als Senior Clinical Research Associate (all genders) Als Senior Clinical Research Associate nimmst du in der klinischen Prüfung unserer Arzneimittel eine Schlüsselrolle ein: Du bist für die Umsetzung globaler Studien in Deutschland verantwortlich. Neben deiner mehrjährigen Monitoringkompetenz ist deine Erfahrung im Studienmanagement und dein Prozess-Know-how gefragt: Innerhalb der wachsenden Abteilung Clinical Site Management [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate (CRA I) / Senior
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the 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 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 [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the 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 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 [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate I
• Wiesbaden
Work-Life-Balance
[. .. ] at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job Description Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the 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 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, [. .. ]
Job vor 13 Tagen bei Jooble gefunden
Alcedis GmbH
• Gießen
Homeoffice möglich Abgeschlossenes Studium
Flexible Arbeitszeiten 30+ Urlaubstage
(Senior)
Clinical Research Associate/ Klinischer Monitor/ Site Manager (m/w/d) - homebased (Region Berlin und Umgebung) bei Alcedis Gmb H softgarden (Senior) Clinical Research Associate/ Klinischer Monitor/ Site Manager (m/w/d) - [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] homebased (Region Berlin und Umgebung) Vollzeit Remote Gießen, Deutschland Mit Berufserfahrung 23.01.26 Als (Senior) Clinical Research Associate/ Klinischer Monitor/ [. .. ]
Job am 23.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
Klinischer Monitor/ Clinical Research Associate (m/w/d)
• Homeoffice
[. .. ] deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] As a Clinical Research Associate, you will: Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, challenging projects. Have excellent communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work. You shall also [. .. ]
Job am 23.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
• Homeoffice
[. .. ] deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] As a Clinical Research Associate, you will: Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, challenging projects. Have excellent communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work. You shall also [. .. ]
Job am 15.01.2026 bei Jooble gefunden
Universitätsklinikum Ulm
Klinischen Monitor/ Clinical Research Associate (CRA) (w/m/d)
• Ulm
Homeoffice möglich Abgeschlossenes Studium Abgeschlossene Ausbildung
Betriebliche Altersvorsorge Jobticket
Für das Zentrum für klinische Studien (ZKS) Ulm suchen wir zum nächstmöglichen Zeitpunkt einen Klinischen Monitor/
Clinical Research Associate (CRA) (w/m/d) Das Universitätsklinikum Ulm steht mit seinen Mitarbeitenden für eine [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] moderne Patientenversorgung mit hoher Qualität, Spitzenforschung und eine auf die Zukunft ausgerichtete medizinische Lehre sowie Ausbildung in attraktiven Berufsfeldern. Voraussetzungen dafür sind qualifizierte und engagierte Mitarbeitende. Das ZKS Ulm ist eine gemeinsame Einrichtung der Medizinischen Fakultät der [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
• Homeoffice
Work-Life-Balance
[. .. ] Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] development. As a Clinical Research Associate II at ICON, youll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II IV, ensuring adherence to applicable regulations and principles of ICH-GCP. You will be [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Clinical Research Associate (CRA) - Oncology
• Homeoffice
Work-Life-Balance
[. .. ] Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] development. As a Clinical Research Associate II at ICON, youll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II IV, ensuring adherence to applicable regulations and principles of ICH-GCP. You will be [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
• Berlin
Clinical Research Associate (CRA) Location: Germany (Remote ) We are seeking a highly motivated Clinical Research Associate (CRA) to support multiple clinical studies. The Contractor will perform monitoring and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] site management activities while ensuring patient safety, regulatory compliance, and high-quality data in accordance with applicable SOPs, study protocols, and ISO 14155:2020. Perform [. .. ]
Job am 14.01.2026 bei Jooble gefunden
TFS Health Science
Clinical Research Associate
• Mainz
[. .. ] that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as a Clinical Research Associate. About this role As part of our FSP team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. This role is dedicated to one of our clients. This role is a full-time role based Germany. Key Responsibilities: Monitor clinical trial sites to ensure [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Alexion Pharmaceuticals
• München
This is what you will do: The
Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at their assigned sites and is an active participant [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in the local study team (s) . The CRA works in close collaboration with local team members (Project Management Clinical Operations (PMCO) , Study Start-Up (SSU) manager, Clinical Study Assistant [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
Clinical Research Associate (Klinischer Monitor)
• Berlin
Clinical Research Associate (CRA) Location: Germany (Remote ) We are seeking a highly motivated Clinical Research Associate (CRA) to support multiple clinical studies. The Contractor will perform monitoring and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] site management activities while ensuring patient safety, regulatory compliance, and high-quality data in accordance with applicable SOPs, study protocols, and ISO 14155:2020. Perform [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
• Berlin
Clinical Research Associate (CRA) Location: Germany (Remote ) Job Description: We are seeking a highly motivated Clinical Research Associate (CRA) to support multiple clinical studies. The Contractor will perform [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] monitoring and site management activities while ensuring patient safety, regulatory compliance, and high-quality data in accordance with applicable SOPs, study protocols, and ISO [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
Experienced Clinical Research Associate (m/w/d) , Multi-Sponsor, Germany
• Frankfurt am Main
Homeoffice möglich
Join IQVIA as a CRA II/ Sr CRA (m/w/d) in our
Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of indications and learn about the diverse scientific approach of the sponsors. Beside establishing strong relationships with the global study team and the involved investigators, you will conduct monitoring on complex [. .. ] client representatives. Qualifications: University Degree in life science or other scientific discipline or apprenticeship in health care. Minimum of two years of on-site monitoring experience Knowledge of applicable clinical research regulatory requirements i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Strong written and verbal communication skills, attention to detail and ability to work in a fast pace environment. Good command of German and English. Flexibility to business travel up to 60 of working time. [. .. ]
Job vor 5 Tagen bei Jooble gefunden
IGES GmbH
• Berlin
Homeoffice möglich
Flexible Arbeitszeiten 30+ Urlaubstage
[. .. ] forschen im Auftrag unserer Kunden darüber hinaus auch zu den Themen Inanspruchnahme, Medical Need, Patientenpräferenzen und Clinical Pathways. Zur Verstärkung unseres Teams in Berlin suchen wir zum [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] nächstmöglichen Zeitpunkt einen Clinical Research Associate/ Klinischen Monitor (m/w/d) . Planung, Vorbereitung und Durchführung von Monitoringvisiten gemäß SOPs (sowohl onsite als auch remote) Fristgerechte Erstellung von Berichten und Follow-Up Dokumentationen der Monitoringvisiten Management und/oder Unterstützung von Studienzentren Sicherstellung der Validität der Studiendaten und Erstellen von Data Queries Teilnahme an Prüfarzttreffen sowie Planung [. .. ]
Job vor 5 Tagen bei Jooble gefunden
IGES GmbH
Clinical Research Associate (m/w/d)
• Berlin
Homeoffice möglich
Flexible Arbeitszeiten 30+ Urlaubstage
[. .. ] forschen im Auftrag unserer Kunden darüber hinaus auch zu den Themen Inanspruchnahme, Medical Need, Patientenpräferenzen und Clinical Pathways. Zur Verstärkung unseres Teams in Berlin suchen wir zum [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] nächstmöglichen Zeitpunkt einen Clinical Research Associate/ Klinischen Monitor (m/w/d) . Planung, Vorbereitung und Durchführung von Monitoringvisiten gemäß SOPs (sowohl onsite als auch remote) Fristgerechte Erstellung von Berichten und Follow-Up Dokumentationen der Monitoringvisiten Management und/oder Unterstützung von Studienzentren Sicherstellung der Validität der Studiendaten und Erstellen von Data Queries Teilnahme an Prüfarzttreffen sowie Planung [. .. ]
Job am 22.01.2026 bei JobMESH gefunden
GBG Forschungs GmbH
• Hessen Neu- Isenburg
Flexible Arbeitszeiten Betriebliche Altersvorsorge Work-Life-Balance
[. .. ] rund 150 Mitarbeitenden gestalten wir Forschung, die international Maßstäbe setzt. Wir arbeiten agil, interdisziplinär und mit echter Begeisterung für wissenschaftlichen Fortschritt, der das Leben von Patientinnen verbessert. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Die Rolle Als Clinical Research Associate (CRA) übernehmen Sie die Verantwortung für die Überwachung und Qualitätssicherung klinischer Studien. Dabei sind Sie die zentrale Schnittstelle zwischen Prüfzentren, Sponsoren und internen Fachbereichen. Die Mission Die Sicherstellung von Qualität und Integrität bei der Durchführung klinischer Prüfungen, um die Sicherheit von Patientinnen und Patienten zu gewährleisten. Clinical Research Associate (CRA) [. .. ]
Job am 20.01.2026 bei Jooble gefunden
Universitätsklinikum Schleswig- Holstein
Clinical Research Associate (m/w/d)
• Kiel
Jobticket
[. .. ] UKSH finden Sie hier: Benefits (uksh. de) Das erwartet Sie: Organisatorische Leitung der Studienzentralen des Dr. Mildred Scheel-Hauses und der Medizinischen Klinik II Umsetzung von Phase I [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Studien (Early Clinical Trials Unit, ECTU) Enge und kollegiale Kooperation mit Studien- und CAR-T-Zell-Koordinator/ innen, Studien-Ärztinnen/ Ärzten, Studien-Apotheke sowie ggfs. weiteren Abteilungen und externen Partnern aus dem Bereich Hochschule und Pharmaindustrie Vertragsmanagement, Budgetverhandlungen, Controlling, Finanzabrechnung und Reporting; Betreuung der Studienpatienten, Terminkoordination; Vorbereitung und Begleitung von Audits/ Inspektionen Etablierung [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor/ Clinical Research Associate
• München
CRA-single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ] when appropriate, to assist employees or applicants to perform the essential functions of the job. Roles within Clinical Monitoring/ CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor/ Clinical Research Associate (m/w/d)
• München
CRA-single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ] when appropriate, to assist employees or applicants to perform the essential functions of the job. Roles within Clinical Monitoring/ CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1 (m/w/d) , Single Sponsor
• Frankfurt am Main
Homeoffice möglich
Join IQVIA as a
Clinical Research Associate 2/ CRA 2 or as Senior Clinical Research Associate 1/ Sr CRA 1 (m/w/d) and work home-based throughout Germany in our single [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sponsor department. You will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our clients. Whether [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Clinical Research Associate/ Klinischer Monitor (m/w/d)
• München
CRA-single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ] when appropriate, to assist employees or applicants to perform the essential functions of the job. Roles within Clinical Monitoring/ CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Clinical Research Associate (Klinischer Monitor)
• München
CRA-single sponsor-Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring [. .. ] audit readiness standards and supports preparation for audit and required follow-up actions. For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. Site support throughout the study lifecycle from site identification through close-out. Chart abstraction activities and data collection Collaboration with Sponsor affiliates, medical science liaisons and local country staff. The SMA II may be requested to train junior staff. Identify and communicate out of scope activities to Lead CRA/ [. .. ] when appropriate, to assist employees or applicants to perform the essential functions of the job. Roles within Clinical Monitoring/ CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. Utilizes data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Research Associate pro Jahr?
Als Clinical Research Associate verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Research Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 133 offene Stellenanzeigen für Clinical Research Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Research Associate Jobs?
Aktuell suchen 19 Unternehmen nach Bewerbern für Clinical Research Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Research Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Research Associate Stellenangebote:
- MEDPACE (22 Jobs)
- Astra Zeneca (19 Jobs)
- ICON (10 Jobs)
- IQVIA (7 Jobs)
- Abb Vie (5 Jobs)
- Thermo Fisher Scientific (4 Jobs)
In welchen Bundesländern werden die meisten Clinical Research Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Research Associate Jobs werden derzeit in Sachsen-Anhalt (17 Jobs), Hessen (16 Jobs) und Berlin (9 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Research Associate Jobs?
Clinical Research Associate Jobs gehören zum Berufsfeld Medizintechnik.
