228 Jobs für Clinical Data Associate
Stellenangebote Clinical Data Associate Jobs
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
• Hamburg
Führungs-/ Leitungspositionen
Responsible for the
clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research
Associate (CRAs) and Investigator sites in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation [. .. ] the site/ CRA in the satisfactory performance and compliance with standards mentioned above. May support clinical project team by providing oversight of study deliverables related to other departments (e. g. Data Management, TMF Operations, etc. ) Oversee regional startup and feasibility activities. Assist in vendor management activities as required per project. Perform review of visit reports for quality, compliance and appropriate site management. Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan. [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
Sr CRA in oncology-Sponsor dedicated-Home Based Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] performed and documented for each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) :Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in and may lead global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical [. .. ]
Job vor 7 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 (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Universität Münster
Fachbereich 14-Geowissenschaften Institute for Geoinformatics Doctoral Research Associate (Wissenschaftlicher Mitarbeiterin, salary level E 13 TV-L) 20.02.2026
• Münster
[. .. ] health and disease. To this end, we combine interdisciplinary research in artificial intelligence, molecular, structural, and cell biology as well as in physiology, biophysics, epi/ genetics, (bio) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] informatics, and multimodal data analysis. Project Description: The project focuses on developing and applying novel machine learning-driven computer vision approaches to analyze complex biological image data. Specifically, you will develop tailored algorithms to quantify testicular histological structures and characterize sperm and cilia motility patterns Your tasks: Developing tailored computer vision and machine learning [. .. ] testicular tissue composition and cell types using foundation models and interactive annotation tools like MARTHA Collaborating with an interdisciplinary team of clinicians and basic scientists to translate algorithmic insights into clinical care Participating in the Integrated Research Training Group Reproduction. MS Ph D-Training Centre in Translational Science Our expectations: Masters degree in Computer Science, Geoinformatics, Physics, Mathematics, or a related quantitative field Strong interest in Machine Learning, Deep Learning, and their application to complex biological or medical imagery Previous experience with [. .. ]
Job vor 7 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 (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Senior Research Associate
• 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 (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
• 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, including appropriate reporting and follow-up for all safety events by site personnel. Ensures safety and protection of study subjects. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in [. .. ]
Job vor 10 Tagen bei Jooble gefunden
Stryker
Associate Manager, Clinical Data Sciences
• Regierungsbezirk Freiburg
Grow Your Career at Stryker as an
Associate Manager,
Clinical Data Science As an Associate Manager for Clinical Data Sciences, you will lead a diverse team of experts and collaborate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with internal and external stakeholders to implement and execute Clinical Data Sciences initiatives for the Instruments division. This role involves driving operational planning, building technical infrastructure to support excellence in evidence [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description Summary Job Description ROLE The Project Manager (PM) is an important member of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Alira Health Clinical team. The PM ensures the efficient implementation of one or more study protocols, works closely with all Clinical team members, and communicates directly with study sponsors and vendors. KEY RESPONSABILITIES Manages clinical research studies to ensure studies are conducted in accordance with approved scope of work/ budget, ICH GCP guidelines, and FDA regulations and within established timelines. Serves as study lead and primary contact for sponsors. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Generates and presents frequent study status updates and reports to sponsor. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Supervises and trains Associate PMs. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Drives and facilitates clinical teamwork and communications to ensure timely attainment of trial milestones. Ensures accuracy of reports and material work product. Provides monthly billing information [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] variety 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 [. .. ] with regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborating with experts on study sites and 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 [. .. ]
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 14155:2020. Key Responsibilities: Conduct monitoring activities including visit preparation, on-site visits, follow-up, site contact, and report writing. Perform remote monitoring and interim site management as required. Support site start-up activities including EC/ CA submissions/ amendments, contract negotiation, and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Clinical Trials Project Associate
• 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 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 [. .. ] medicine, science, or equivalent Previous monitoring experience in medium-sized studies, including study start-up and close-out Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent written and verbal communication in both English and German Ability to work to tight deadlines Availability to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our [. .. ]
Job am 14.01.2026 bei Jooble gefunden
TFS Health Science
• Mainz
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team 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 protocol, GCP, and regulatory compliance Conduct site visits (initiation, monitoring, and close-out) and prepare visit reports Verify source data and ensure accurate, timely data entry Support site staff with study procedures and documentation Identify, escalate, and help resolve study issues and risks Qualifications: Bachelors degree in life sciences or a related field 5+ years of CRA or clinical research monitoring experience Strong knowledge of ICH-GCP and regulatory requirements [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Freelance CRA Germany
• München
Freiberuflich
Freelance CRA 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] performed and documented for each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Your Personal AI
• Bremen
Licensed dentists needed for compensated freelance engagement involving documentation of German-language dental consultations. Project focuses on creating simulated
clinical conversations for professional development resources. Single session (1-2 hours) Any [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] professional or quiet office setting PROFESSIONAL RESPONSIBILITIES Selected participants will collaborate with a dental team member to produce authentic clinical dialogue recordings. Working from structured conversation guides, professionals will simulate routine dental consultations while maintaining natural communication patterns. REGULATORY COMPLIANCE Project maintains strict adherence to: Simulated content protocols (no patient information) GDPR data protection standards Professional service standards Current dental licensure or active residency Professional-level German fluency (C1 minimum) ; Dental colleague available as conversation partner Schedule flexibility for project participation 74896568 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Antal Sp. z o. o.
Klinischer Monitor/ Clinical Research Associate
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and 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 remote monitoring and interim site management as required. Support site start-up activities including EC/ CA submissions/ amendments, contract negotiation, and documentation preparation/ collection. Report non-compliance of investigators with their Clinical Study Agreements (CSAs) to the Client. Support [. .. ]
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 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 [. .. ] medicine, science, or equivalent Previous monitoring experience in medium-sized studies, including study start-up and close-out Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent written and verbal communication in both English and German Ability to work to tight deadlines Availability to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Incyte Corporation
Associate Director, Medical Affairs Dermatology (Atopic Dermatitis) (m/f/d)
• München
Führungs-/ Leitungspositionen
The
Associate Director, Medical Affairs Dermatology (Atopic Dermatitis) , is part of the Medical Affairs Team and represents his/ her area of responsibility towards external and internal stakeholders. Owing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to his/ her profound understanding of the respective treatment area and extensive network the Associate Director Medical Affairs Dermatology establishes and fosters collaborations with external partners and provides a bridge between clinical development, medical affairs and the commercial organization at a senior mastery level. He/ she provides critical insights into the countrys medical affairs plan for the respective disease areas, ensuring that it complements the companys development plan and adheres to the highest scientific standards. Constantly build and maintain expertise in the assigned areas IAI areas (dermatologic entities, drugs) , regarding available literature, treatment options, disease environment and product data; Actively contributes to the advancement of the national development program within his/ her area of responsibility Actively participates whenever feasible-in medical scientific exchanges within medical/ scientific community and fosters collaborations with key external stakeholders Identifies scientific questions relevant to the German healthcare landscape and develops and executes a strategy [. .. ]
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 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 [. .. ] medicine, science, or equivalent Previous monitoring experience in medium-sized studies, including study start-up and close-out Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent written and verbal communication in both English and German Ability to work to tight deadlines Availability to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
CRA II
• 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 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 [. .. ] medicine, science, or equivalent Previous monitoring experience in medium-sized studies, including study start-up and close-out Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent written and verbal communication in both English and German Ability to work to tight deadlines Availability to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Clinical Trials Assistant-Oncology
• 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 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 [. .. ] medicine, science, or equivalent Previous monitoring experience in medium-sized studies, including study start-up and close-out Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent written and verbal communication in both English and German Ability to work to tight deadlines Availability to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Alexion Pharmaceuticals
Clinical Research Associate
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 (SSU) manager, Clinical Study Assistant [. .. ] and experience may take on additional study level responsibilities and tasks as needed (e. g. Lead CRA, etc) . You will be responsible for: Performing identification, selection, initiation, monitoring, site data review and closeout activities/ visits (remote and onsite) , as well as remote data checks, in accordance with the timelines specified in the study specific Clinical Monitoring Plan (CMP) . Driving performance at the sites. Proactively identifying and ensuring timely resolution to study-related issues and escalates them as appropriate. [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Your Personal AI
Associate-German Speaking
• Bremen
Licensed dentists needed for compensated freelance engagement involving documentation of German-language dental consultations. Project focuses on creating simulated
clinical conversations for professional development resources. Single session (1-2 hours) Any [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] professional or quiet office setting PROFESSIONAL RESPONSIBILITIES Selected participants will collaborate with a dental team member to produce authentic clinical dialogue recordings. Working from structured conversation guides, professionals will simulate routine dental consultations while maintaining natural communication patterns. REGULATORY COMPLIANCE Project maintains strict adherence to: Simulated content protocols (no patient information) GDPR data protection standards Professional service standards Current dental licensure or active residency Professional-level German fluency (C1 minimum) ; Dental colleague available as conversation partner Schedule flexibility for project participation 74896566 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Clinical Research Associate-Oncology
• 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 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 [. .. ] medicine, science, or equivalent Previous monitoring experience in medium-sized studies, including study start-up and close-out Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data Excellent written and verbal communication in both English and German Ability to work to tight deadlines Availability to travel least 60 of the time (international and domestic-fly and drive) and should possess a valid driving license What ICON can offer you: Our success depends on the quality of our [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and 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 remote monitoring and interim site management as required. Support site start-up activities including EC/ CA submissions/ amendments, contract negotiation, and documentation preparation/ collection. Report non-compliance of investigators with their Clinical Study Agreements (CSAs) to the Client. Support [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical data associate pro Jahr?
Als Clinical data associate verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Data Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 228 offene Stellenanzeigen für Clinical Data Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Data Associate Jobs?
Aktuell suchen 34 Unternehmen nach Bewerbern für Clinical Data Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Data Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Data Associate Stellenangebote:
- ICON (19 Jobs)
- Astra Zeneca (19 Jobs)
- IQVIA (10 Jobs)
- Alimentiv (7 Jobs)
- TFS Health Science (7 Jobs)
- IGES GmbH (5 Jobs)
In welchen Bundesländern werden die meisten Clinical Data Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Data Associate Jobs werden derzeit in Bayern (26 Jobs), Berlin (17 Jobs) und Hessen (16 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Data Associate Jobs?
Clinical Data Associate Jobs gehören zum Berufsfeld Medizintechnik.
