607 Jobs für Clinical Monitoring
Stellenangebote Clinical Monitoring Jobs
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
• Hamburg
Führungs-/ Leitungspositionen
[. .. ] effective interpersonal and organizational skills. Demonstrate the following attributes: proactive, detail oriented, task-driven and highly organized. Demonstrate the critical elements of GCPs and local regulations as they [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relate to clinical monitoring, IRB/ EC and Investigator responsibilities. Demonstrated ability in report writing and strong ability to critically understand clinical research documents. Ability to handle multiple tasks to meet deadlines in a dynamic environment. Working Conditions Home-based 58, 000-96, 500 a year Bonus Accommodations for persons with disabilities are available on [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 accurate and complete via review of site source documents and medical records Applies query resolution techniques remotely and [. .. ]
Job am 23.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
• Homeoffice
[. .. ] communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work. Perform and coordinate all [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently. Benefit from award winning training programmes that will assist your technical and professional skills and knowledge. Keys to Success: Education University degree in a life-sciences field Experience At least 6 months independent, on-site monitoring experience or at [. .. ]
Job am 23.01.2026 bei Jooble gefunden
Clinical Trial Lead-single client-Austria, Germany or the UK
• München
[. .. ] management reports for clients and management. May participate in bid defense meetings where presented as potential project manager. May be required to line manage other project management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team members and clinical monitoring staff. Bachelors Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience. Strong ability to manage time and work independently. We are always excited to connect with great talent. By expressing your interest, youll be added to our talent pipeline and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
Freiberuflich
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 accurate and complete. Applies query resolution techniques remotely and on site, and provides guidance to site staff [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Socra Tec R D GmbH
CRA (m/w/d)
• Oberursel
Abgeschlossenes Studium Abgeschlossene Ausbildung
[. .. ] Initiierungs-, Within-Study und Close Out Besuchen) Koordination der Kommunikation mit Prüfstellen, Sponsoren und weiteren Projektbeteiligten zur Sicherstellung eines reibungslosen Studienablaufs Unterstützung bei der Einarbeitung neuer Mitarbeiter:innen im [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Bereich Clinical Monitoring, Unterstützung bei der Vorbereitung und Durchführung von Audits und Inspektionen Unterstützung bei der Weiterentwicklung von Prozessen und der Pflege von SOPs Abgeschlossenes naturwissenschaftliches Studium oder eine abgeschlossene Ausbildung im medizinischen oder medizinisch-technischen Bereich 2 Jahre Erfahrung als klinischer Monitor/ Studienkoordinator/ Projektmanager ausgezeichnete mündliche und schriftliche Kommunikationsfähigkeiten in Deutsch und [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Socra Tec R D GmbH
• Oberursel
Abgeschlossenes Studium Abgeschlossene Ausbildung
[. .. ] eines Monitoring-Teams (Lead Monitoring) sowie Sicherstellung einheitlicher Qualitätsstandards über alle Prüfstellen großer multizentrischer Studien gemäß CTR, ICH-Richtlinien und internen SOPs Unterstützung bei der Einarbeitung neuer Mitarbeiter:innen im [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Bereich Clinical Monitoring, Unterstützung bei der Vorbereitung und Durchführung von Audits und Inspektionen Unterstützung bei der Weiterentwicklung von Prozessen und der Pflege von SOPs IHR PROFIL Abgeschlossenes naturwissenschaftliches Studium oder eine abgeschlossene Ausbildung im medizinischen oder medizinisch-technischen Bereich Mind. 2 Jahre Erfahrung als klinischer Monitor/ Studienkoordinator/ Projektmanager Hohes Maß an Selbständigkeit, Team-[. .. ]
Job am 14.01.2026 bei Jooble gefunden
Alexion Pharmaceuticals
Clinical Research Associate
• München
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. Training, supporting, and advising Investigators and site staff in study-related matters, including Risk Based Quality Management (RBQM) principles. Development of recruitment plans with each site and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
• Frankfurt am Main
Homeoffice möglich
[. .. ] and clinical data flow. Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. May accompany CRAs on site visits [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to assist with clinical monitoring duties upon completion of required training. REQUIRED KNOWLEDGE, SKILLS AND EXPERIENCE Bachelor s or higher-level degree preferable in life science or High School Diploma and apprenticeship in life science, the medical or pharmaceutical field or office management. Preferable 2 years or more of experience as Clinical Trials Assistant or [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
Clinical Operations Lead
• Frankfurt am Main
Führungs-/ Leitungspositionen
[. .. ] effective interpersonal and organizational skills. Demonstrate the following attributes: proactive, detail oriented, task-driven and highly organized. Demonstrate the critical elements of GCPs and local regulations as they [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] relate to clinical monitoring, IRB/ EC and Investigator responsibilities. Demonstrated ability in report writing and strong ability to critically understand clinical research documents. Ability to handle multiple tasks to meet deadlines in a dynamic environment. Working Conditions Home-based 58, 000-96, 500 a year Bonus Accommodations for persons with disabilities are available on [. .. ]
Job gestern bei Jooble gefunden
• München
[. .. ] not only make Syneos Health easier to work with, but to make us easier to work for. Why Syneos Health supportive and engaged line management; Responsible for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/ GCP/ regulatory compliance and data integrity. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT) . Reviews the study scope of [. .. ]
Job gestern bei JobMESH gefunden
Thermo Fisher Scientific
CRA II/ Sr CRA-FSP-Germany (m/f/d)
• Germany
[. .. ] communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work. Perform and coordinate all [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently. Benefit from award winning training programmes that will assist your technical and professional skills and knowledge. Keys to Success: Education University degree in a life-sciences field Experience At least 6 months independent, on-site monitoring experience or at [. .. ]
Job vor 4 Tagen bei Jooble gefunden
• München
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 accurate and complete via review of site source documents and medical records Applies query resolution techniques remotely and [. .. ]
Job vor 7 Tagen bei JobMESH gefunden
Thermo Fisher Scientific
Assistant CRA (m/f/d)
• Baden- Wurttemberg
[. .. ] related field. Current PPD CRAs qualify to be considered for this role without having the degree requirements. Experience Prior clinical research experience 0-1 year as well as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] knowledge of clinical monitoring through classwork/ training that provides the required knowledge skills and abilities. In some cases, previous experience in a clinical environment where experience is gained in clinical trials, data management, medical terminology, medical research or health care or experience in a health sciences field with formal training in medical terminology and [. .. ]
Job vor 12 Tagen bei Jooble gefunden
• München
[. .. ] with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Summary Roles within Clinical Monitoring/ CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. These roles involve individual contributors with responsibility in a [. .. ]
Job am 22.01.2026 bei Jooble gefunden
Clinical Trial Lead-single client-Austria, Germany or the UK
• München
[. .. ] management reports for clients and management. May participate in bid defense meetings where presented as potential project manager. May be required to line manage other project management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team members and clinical monitoring staff. Bachelors Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience. Strong ability to manage time and work independently. We are always excited to connect with great talent. By expressing your interest, youll be added to our talent pipeline and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
• Karlsruhe
[. .. ] related field. Current PPD CRAs qualify to be considered for this role without having the degree requirements. Experience Prior clinical research experience 0-1 year as well as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] knowledge of clinical monitoring through classwork/ training that provides the required knowledge skills and abilities. In some cases, previous experience in a clinical environment where experience is gained in clinical trials, data management, medical terminology, medical research or health care or experience in a health sciences field with formal training in medical terminology and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor/ Clinical Research Associate
• München
[. .. ] the ISF with the Trial Master File (TMF) . Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] SOPs and Clinical Monitoring Plan/ Site Management Plan. Supports subject/ patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. For assigned activities, understands project scope, budgets, and timelines; manages site-level activities/ communication to ensure project objectives, deliverables [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
[. .. ] compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] job. Roles within Clinical Monitoring/ CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. The majority of time is spent contributing to the [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Freelance CRA Germany
• München
Freiberuflich
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 accurate and complete. Applies query resolution techniques remotely and on site, and provides guidance to site staff [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Klinischer Monitor/ Clinical Research Associate (m/w/d)
• München
[. .. ] the ISF with the Trial Master File (TMF) . Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] SOPs and Clinical Monitoring Plan/ Site Management Plan. Supports subject/ patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. For assigned activities, understands project scope, budgets, and timelines; manages site-level activities/ communication to ensure project objectives, deliverables [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
CRA Assistant (m/w/d)
• Karlsruhe
[. .. ] files and complying with CTMS and e TMF data stewardship. Education Bachelors Degree in a life science-related field. Prior clinical research experience 0-1 year as well as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] knowledge of clinical monitoring through classwork/ training that provides the required knowledge skills and abilities. In some cases, previous experience in a clinical environment where experience is gained in clinical trials, data management, medical terminology, medical research or health care or experience in a health sciences field with formal training in medical terminology and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Socra Tec R D GmbH
Klinischer Monitor/ CRA (m/w/d)
• Erfurt
Abgeschlossenes Studium Abgeschlossene Ausbildung
[. .. ] eines Monitoring-Teams (Lead Monitoring) sowie Sicherstellung einheitlicher Qualitätsstandards über alle Prüfstellen großer multizentrischer Studien gemäß CTR, ICH-Richtlinien und internen SOPs Unterstützung bei der Einarbeitung neuer Mitarbeiter:innen im [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Bereich Clinical Monitoring, Unterstützung bei der Vorbereitung und Durchführung von Audits und Inspektionen Unterstützung bei der Weiterentwicklung von Prozessen und der Pflege von SOPs IHR PROFIL Abgeschlossenes naturwissenschaftliches Studium oder eine abgeschlossene Ausbildung im medizinischen oder medizinisch-technischen Bereich Mind. 2 Jahre Erfahrung als klinischer Monitor/ Studienkoordinator/ Projektmanager Hohes Maß an Selbständigkeit, Team-[. .. ]
Job am 14.01.2026 bei Jooble gefunden
CRA-single sponsor-Germany
• München
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 accurate and complete. Applies query resolution techniques remotely and on site, and provides guidance to site staff [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Clinical Research Associate/ Klinischer Monitor (m/w/d)
• München
[. .. ] the ISF with the Trial Master File (TMF) . Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] SOPs and Clinical Monitoring Plan/ Site Management Plan. Supports subject/ patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. For assigned activities, understands project scope, budgets, and timelines; manages site-level activities/ communication to ensure project objectives, deliverables [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Monitoring pro Jahr?
Als Clinical Monitoring verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Monitoring Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 607 offene Stellenanzeigen für Clinical Monitoring Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Monitoring Jobs?
Aktuell suchen 109 Unternehmen nach Bewerbern für Clinical Monitoring Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Monitoring Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Monitoring Stellenangebote:
- ICON (22 Jobs)
- Thermo Fisher Scientific (21 Jobs)
- Astra Zeneca (21 Jobs)
- IQVIA (17 Jobs)
- Abb Vie (10 Jobs)
- Medline Europe (10 Jobs)
In welchen Bundesländern werden die meisten Clinical Monitoring Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Monitoring Jobs werden derzeit in Bayern (67 Jobs), Baden-Württemberg (45 Jobs) und Sachsen-Anhalt (39 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Monitoring Jobs?
Clinical Monitoring Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
