73 Jobs für Clinical Research Associate
Stellenangebote Clinical Research Associate Jobs
Job vor 11 Tagen bei Mindmatch.ai gefunden
Randstad Belgium
• Berlin, BE
Angebote von Zeitarbeitsunternehmen
Freelance
Clinical Research Associate (CRA) Germany Medical Devices Are you an experienced Clinical Research Associate looking for your next high-impact freelance project in the medical device sector? Do you thrive [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in a hybrid role that combines the comfort of working from home with the energy of on-site hospital visits? Randstad Professional is [. .. ]
Job vor 14 Tagen bei Mindmatch.ai gefunden
Upsilon Global
Clinical Research Associate
• Munich, BY
Location: Germany-Frankfurt Hamburg Therapeutic Area: Oncology Contract Type: Freelance/ Independent Contractor Commitment: Approximately 0.50.8 FTE Number of Opportunities: 5 About the Opportunity Join an established global
clinical research organisation delivering [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] innovative, high-quality clinical development solutions across a range of therapeutic areas. With strong expertise in Oncology and Haematology, the organisation supports clinical studies across solid and haematological cancers and is committed to advancing the development of innovative treatments for patients. We are currently seeking experienced freelance Senior [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
ARTO
• Essen, NW
The client is preparing the launch of an international randomized
clinical trial (RCT) across Europe and the United States to support marketing authorization. Due to the absence of a full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CRO model, key activities will be managed internally. We are therefore seeking experienced Senior CRAs to support site selection and regulatory submissions. Scope of the mission-Site selection (including on-site [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
RBW Consulting
Clinical Research Associate II
• Berlin, BE
Clinical Research Associate II (CRA II) Location: Germany Based, Covering DACH Region Join a Global CRO Making a Difference Our client is a highly respected global CRO with deep expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in complex and specialist therapeutic areas. Consistently outperforming the wider market, they have built an excellent reputation for scientific expertise, operational excellence, and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
ARTO
Senior Clinical Research Associate
• Cologne, NW
The client is preparing the launch of an international randomized
clinical trial (RCT) across Europe and the United States to support marketing authorization. Due to the absence of a full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CRO model, key activities will be managed internally. We are therefore seeking experienced Senior CRAs to support site selection and regulatory submissions. Scope of the mission-Site selection (including on-site [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
RBW Consulting
Clinical Research Associate II
• Leipzig, SN
Clinical Research Associate II (CRA II) Location: Germany Based, Covering DACH Region Join a Global CRO Making a Difference Our client is a highly respected global CRO with deep expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in complex and specialist therapeutic areas. Consistently outperforming the wider market, they have built an excellent reputation for scientific expertise, operational excellence, and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
ARTO
Senior Clinical Research Associate
• Stuttgart, BW
The client is preparing the launch of an international randomized
clinical trial (RCT) across Europe and the United States to support marketing authorization. Due to the absence of a full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] CRO model, key activities will be managed internally. We are therefore seeking experienced Senior CRAs to support site selection and regulatory submissions. Scope of the mission-Site selection (including on-site [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
RBW Consulting
Clinical Research Associate II
• Munich, BY
Clinical Research Associate II (CRA II) Location: Germany Based, Covering DACH Region Join a Global CRO Making a Difference Our client is a highly respected global CRO with deep expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in complex and specialist therapeutic areas. Consistently outperforming the wider market, they have built an excellent reputation for scientific expertise, operational excellence, and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
RBW Consulting
• Dortmund, NW
Clinical Research Associate II (CRA II) Location: Germany Based, Covering DACH Region Join a Global CRO Making a Difference Our client is a highly respected global CRO with deep expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in complex and specialist therapeutic areas. Consistently outperforming the wider market, they have built an excellent reputation for scientific expertise, operational excellence, and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Advanced Resource Managers
Clinical Research Associate
• Essen, NW
[. .. ] on data integrity, patient safety, and protocol compliance. Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations. Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines. Assist in the development and review of study-related documents, including protocols, informed consent [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Advanced Resource Managers
Clinical Research Associate
• Berlin, BE
[. .. ] on data integrity, patient safety, and protocol compliance. Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations. Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines. Assist in the development and review of study-related documents, including protocols, informed consent [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Advanced Resource Managers
Clinical Research Associate
• Leipzig, SN
[. .. ] on data integrity, patient safety, and protocol compliance. Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations. Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines. Assist in the development and review of study-related documents, including protocols, informed consent [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
ARTO
Senior Clinical Research Associate
• Berlin, BE
The client is preparing the launch of an international randomized
clinical trial (RCT) across Europe and the United States to support marketing authorization. Due to the absence of a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] full CRO model, key activities will be managed internally. We are therefore seeking experienced Senior CRAs to support site selection and regulatory submissions. Scope of the mission-Site selection (including on-site [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Advanced Resource Managers
Clinical Research Associate
• Dortmund, NW
[. .. ] on data integrity, patient safety, and protocol compliance. Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations. Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines. Assist in the development and review of study-related documents, including protocols, informed consent [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
RBW Consulting
Clinical Research Associate II
• Hamburg, HH
Clinical Research Associate II (CRA II) Location: Germany Based, Covering DACH Region Join a Global CRO Making a Difference Our client is a highly respected global CRO with deep [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise in complex and specialist therapeutic areas. Consistently outperforming the wider market, they have built an excellent reputation for scientific expertise, operational excellence, and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
ARTO
Senior Clinical Research Associate
• Munich, BY
The client is preparing the launch of an international randomized
clinical trial (RCT) across Europe and the United States to support marketing authorization. Due to the absence of a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] full CRO model, key activities will be managed internally. We are therefore seeking experienced Senior CRAs to support site selection and regulatory submissions. Scope of the mission-Site selection (including on-site [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Advanced Resource Managers
Clinical Research Associate
• Düsseldorf, NW
[. .. ] on data integrity, patient safety, and protocol compliance. Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations. Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines. Assist in the development and review of study-related documents, including protocols, informed consent [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
Advanced Resource Managers
Clinical Research Associate
• Frankfurt
[. .. ] on data integrity, patient safety, and protocol compliance. Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations. Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines. Assist in the development and review of study-related documents, including protocols, informed consent [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
Advanced Resource Managers
Clinical Research Associate
• Hamburg, HH
[. .. ] on data integrity, patient safety, and protocol compliance. Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations. Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines. Assist in the development and review of study-related documents, including protocols, informed consent [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
Advanced Resource Managers
Clinical Research Associate
• Stuttgart, BW
[. .. ] on data integrity, patient safety, and protocol compliance. Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations. Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines. Assist in the development and review of study-related documents, including protocols, informed consent [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
Advanced Resource Managers
Clinical Research Associate
• Cologne, NW
[. .. ] on data integrity, patient safety, and protocol compliance. Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations. Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines. Assist in the development and review of study-related documents, including protocols, informed consent [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
Advanced Resource Managers
Clinical Research Associate
• Munich, BY
[. .. ] on data integrity, patient safety, and protocol compliance. Develop and maintain strong relationships with investigative sites, ensuring effective communication and collaboration throughout the duration of the study. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Review and verify clinical data, source documents, and study records to ensure accuracy, completeness, and compliance with applicable regulations. Proactively identify and resolve study-related issues and discrepancies, escalating as necessary to ensure timely resolution and adherence to project timelines. Assist in the development and review of study-related documents, including protocols, informed consent [. .. ]
Job am 11.09.2026 bei Neuvoo.com gefunden
Upsilon Global
Clinical Research Associate
• Hessen Frankfurt
Location: Germany-Frankfurt Hamburg Therapeutic Area: Oncology Contract Type: Freelance/ Independent Contractor Commitment: Approximately 0.50.8 FTE Number of Opportunities: 5 About the Opportunity Join an established global
clinical research organisation delivering [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] innovative, high-quality clinical development solutions across a range of therapeutic areas. With strong expertise in Oncology and Haematology, the organisation supports clinical studies across solid and haematological cancers and is committed to advancing the development of innovative treatments for patients. We are currently seeking experienced freelance Senior [. .. ]
Job am 11.09.2026 bei Neuvoo.com gefunden
Upsilon Global
Clinical Research Associate
• Berlin
Location: Germany-Frankfurt Hamburg Therapeutic Area: Oncology Contract Type: Freelance/ Independent Contractor Commitment: Approximately 0.50.8 FTE Number of Opportunities: 5 About the Opportunity Join an established global
clinical research organisation delivering [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] innovative, high-quality clinical development solutions across a range of therapeutic areas. With strong expertise in Oncology and Haematology, the organisation supports clinical studies across solid and haematological cancers and is committed to advancing the development of innovative treatments for patients. We are currently seeking experienced freelance Senior [. .. ]
Job am 11.09.2026 bei Neuvoo.com gefunden
Upsilon Global
Clinical Research Associate
• Bavaria Munich
Location: Germany-Frankfurt Hamburg Therapeutic Area: Oncology Contract Type: Freelance/ Independent Contractor Commitment: Approximately 0.50.8 FTE Number of Opportunities: 5 About the Opportunity Join an established global
clinical research organisation delivering [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] innovative, high-quality clinical development solutions across a range of therapeutic areas. With strong expertise in Oncology and Haematology, the organisation supports clinical studies across solid and haematological cancers and is committed to advancing the development of innovative treatments for patients. We are currently seeking experienced freelance Senior [. .. ]
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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 73 offene Stellenanzeigen für Clinical Research Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Research Associate Jobs?
Aktuell suchen 6 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:
- Advanced Resource Managers (16 Jobs)
- Upsilon Global (12 Jobs)
- ARTO (5 Jobs)
- RBW Consulting (5 Jobs)
- Randstad Belgium (1 Job)
In welchen Bundesländern werden die meisten Clinical Research Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Research Associate Jobs werden derzeit in Berlin (13 Jobs), Nordrhein-Westfalen (10 Jobs) und Baden-Württemberg (6 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Research Associate Jobs?
Clinical Research Associate Jobs gehören zum Berufsfeld Medizintechnik.
