129 Jobs für Drug Monitoring
Stellenangebote Drug Monitoring Jobs
Job am 18.08.2026 bei Jobleads gefunden
• Bremen
[. .. ] solutions in preclinical imaging, clinical phenomics research, proteomics and multiomics, spatial and single-cell biology, functional structural and condensate biology, as well as in clinical microbiology, molecular diagnostics [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and therapeutic drug monitoring. For more information, please visit Today, more than 11, 000 employees at over 100 locations are working on this permanent challenge to make the world a better place. As a Java Desktop Developer, you will contribute to the development of desktop applications used to control advanced mass spectrometry instruments. You [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Facharzt (w/m/d) für Laboratoriumsmedizin mit primärem Standort Altona
• Hamburg
[. .. ] Dann suchen wir genau Sie Zu Ihren Aufgaben gehören: Vielseitiges und abwechslungsreiches Arbeitsspektrum: Unterstützung eines fachlich hoch qualifizierten Teams in der Laboratoriumsmedizin mit Schwerpunkten in der klassischen [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Klinischen Chemie, Proteinchemie, Drug Monitoring, Hämatologie, Basisgerinnung und Immunhämatologie Beratung und Dialog: Konsiliarische Beratung und fachlicher Dialog mit unseren ambulant und stationär tätigen Kollegen und Kolleginnen sowie fachärztliche Hintergrunddienst Tätigkeit für unsere Kliniken Betreuung von bundesweiten Standorten: Betreuung/ Leitung von MEDILYS Laborstandorten überwiegend in hybrider Zusammenarbeit Stateofthe Art Technologie: Begleitung und Betreuung unserer Innovationsprojekte, z. [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
• Madlow, Brandenburg
Abgeschlossene Ausbildung
[. .. ] Jahren für Präzision, Zuverlässigkeit und höchsten Qualitätsanspruch in der medizinischen Diagnostik. Als akkreditiertes Labor bieten wir ein breites Spektrum von medizinisch-diagnostischen Analysen an. Besondere Schwerpunkte sind dabei [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] das therapeutische Drug-Monitoring, mikrobiologische Diagnostik, eine umfangreiche Analytik auf Spurenelemente und Metalle, Immundefek-t Diagnostik bzw. immunologische Diagnostik sowie Lymphom- und Leukämie-Diagnostik. Eine umfassende Hygieneberatung sowie hygienebezogene Laboruntersuchungen komplettieren unser Leistungsangebot. Zur Verstärkung unseres Teams suchen wir zum nächstmöglichen Zeitpunkt für ein unbefristetes Arbeitsverhältnis eine MTLA (m/w/d) in Vollzeit. Ihre Aufgaben [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Fachärztin/ Facharzt für Laboratoriumsmedizin (m/w/d)
• München, Bayern
Abgeschlossenes Studium
Betriebliche Altersvorsorge
[. .. ] Diagnostik für Körperflüssigkeiten von Patienten des TUM Klinikums Deutsches Herzzentrum durchführt. Das Analysenspektrum umfasst klinisch-chemische, hämatologische, hämostaseologische, immunologische, endokrinologische, serologische und Urin-Analysen sowie Spezialanalytik im Bereich Hämostaseologie, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Therapeutisches Drug Monitoring und Molekularbiologie. Das Institut für Laboratoriumsmedizin sucht zum nächstmöglichen Zeitpunkt in Voll-oder Teilzeit eine/n Fachärztin/ Facharzt für Laboratoriumsmedizin (m/w/d) Ihr Aufgabengebiet Fachliche und organisatorische Betreuung der Labordiagnostik Fachliche Vertretung der Laborleitung Mitwirkung beim Management von POCT und Labor-IT Beratung der Stationen und Ambulanzen in labormedizinischen [. .. ]
Neu Job vor 3 Std. bei StepStone gefunden
Astra Zeneca
• bundesweit
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] Therapy (m/f/d) - Field Based The Local Study Associate Director (LSAD) (w/f/d) , Cell Therapy is a key member of the country Cell Therapy Site Management
Monitoring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] organisation. You will lead Local Study Team (s) at country level and be accountable for delivering committed components of clinical studies according to agreed resources, budget and timelines. This field-based role combines strategic study leadership with hands-on responsibility for site management, monitoring, feasibility, recruitment and retention. You will [. .. ] Your Profile: Bachelors degree in life sciences, medicine or a comparable field; an advanced scientific degree is advantageous. Approximately 5 years or more of experience in clinical research or pharmaceutical drug development. Several years of hands-on clinical study monitoring experience, including site qualification, initiation, routine monitoring and close-out activities. Experience leading complex clinical studies and/or Local Study Teams in a matrix environment. Excellent knowledge of ICH-GCP and relevant local regulatory requirements, with a strong understanding of clinical [. .. ]
Job am 07.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Cologne, NW
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Tigermed
• Düsseldorf, NW
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Leipzig, SN
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Berlin, BE
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Hamburg, HH
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Stuttgart, BW
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Frankfurt
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Dortmund, NW
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 05.09.2026 bei Mindmatch.ai gefunden
Tigermed
Contractor CRA Germany
• Essen, NW
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Neu Job vor 3 Std. bei Neuvoo.com gefunden
Paul- Ehrlich- Institut
• Hessen
Jobticket Work-Life-Balance
[. .. ] policymakers, and the business sector. Department Z5 Information Technology ensures, through all its services, that the operation and further development of information technology, as well as the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] electronic maintenance of drug data at the PEI, are carried out while ensuring the availability, integrity, and confidentiality of all data at the PEI. In doing so, Division Z5 follows the best practices of the IT Infrastructure Library (ITIL) . Your Responsibilities Ensuring the continuous operation of the document management and workflow system DMS/ VBS (Fabasoft e GOV-Suite and Mindbreeze) Administration, monitoring, maintenance, and further development of servers and databases, including updates and troubleshooting Analysis, diagnosis, and resolution of system and application issues to troubleshoot problems, as well as performing updates and version upgrades Programming, as well as the creation and customization of scripts and databases Planning, monitoring, and support of interfaces [. .. ]
Job am 05.09.2026 bei Neuvoo.com gefunden
Tigermed
Contractor CRA Germany
• Hamburg
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 05.09.2026 bei Neuvoo.com gefunden
Tigermed
Contractor CRA Germany
• Saxony Leipzig
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 05.09.2026 bei Neuvoo.com gefunden
Tigermed
Contractor CRA Germany
• Berlin
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 05.09.2026 bei Neuvoo.com gefunden
Tigermed
Contractor CRA Germany
• North Rhine- Westphalia Cologne
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 05.09.2026 bei Neuvoo.com gefunden
Tigermed
Contractor CRA Germany
• Baden- Württemberg Stuttgart
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 05.09.2026 bei Neuvoo.com gefunden
Tigermed
Contractor CRA Germany
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Job am 05.09.2026 bei Neuvoo.com gefunden
Tigermed
Contractor CRA Germany
• Hessen Frankfurt
Responsibilities (a) Site management Study site selection, initiation (SIV) and clinical
monitoring. Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not limited to adequate resources and experience. Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and [. .. ] studies. Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating. Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study. Assemble site specific EC submission dossier, and ensure submission to EC. Training Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements. Conduct site initiation to ensure that the site [. .. ]
Neu Job vor 3 Std. bei Mindmatch.ai gefunden
Fresenius Kabi Austria
Senior Manager Quality Operations (m/f/d)
• AT- 6 Graz
Homeoffice möglich
Jobticket
[. .. ] Programs from development to commercial Manage GMP compliance during Tech Transfer of manufacturing activities of Combination Product Manage internal and external Change Controls, Deviations, Events, CAPAs, etc. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] , related to Drug Substance, Drug Product and Combination Products Contribute to QM programs and GMP/ GDP/ MDR compliance activities as appropriate Manage GMP/ GDP/ MDR quality oversight (qualification, approval, monitoring) of C (D) MOs, Testing Labs, Medical Devices suppliers, packagers and carriers A BA/ BS, MA/ MS or Ph D in a technical or engineering discipline or related field Minimum seven years experience in a Quality function with increasing levels of responsibility in the biotech, lifescience or pharmaceutical industry Strong understanding [. .. ]
Job gestern bei Mindmatch.ai gefunden
Louisiana State University
Lead Worker-Anesthesia
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] services, and all Large Animal clinical services while also providing leadership and support to full-time, part-time, and student technicians/ assistants working within the area. Responsibilities include preparing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and monitoring patients before, during, and after anesthesia; assisting faculty clinicians and house officers with anesthetic procedures; and ensuring the safe delivery of anesthesia in accordance with established hospital protocols. The individual must possess expertise in the safe handling and restraint of small animals and be able to provide instruction and guidance [. .. ] work a variety of shifts including nights, weekends, holidays, and on-call/ relief shifts. Due to the nature of this position and/or responsibilities, this position is subject to random drug alcohol testing in accordance with University Policy Statement 67 Required to be capable of lifting 50+ pounds, standing, sitting, walking, bending, reaching above the shoulder, reaching below the shoulder, vision near sight, vision far sight, climbing, crawling, twisting, pushing/ pulling, grasping, and squatting. Essential Personnel-This position may be required [. .. ]
Job gestern bei Mindmatch.ai gefunden
Rivia
Senior AI Engineer
• AT- 2 Lavamünd
[. .. ] to significantly more efficient trial execution. In March 2026, Rivia raised its 15M Series A led by Earlybird Venture Capital. Rivias ambition is to become the standard [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] infrastructure for modern drug development, transforming how trials are executed end-to-end. About AI Engineering at Rivia Given the highly complex nature of clinical trials and how they interface with our technology, the AI Engineering team at Rivia is pivotal in ensuring our clients achieve their desired outcomes and derive maximum value from our platform. The team designs and operates agentic, production-grade AI workflows that power critical monitoring, data quality, and insight-generation capabilities for clinical trial stakeholders. By building reliable, auditable, and scalable AI systems, AI Engineering helps transform fragmented clinical data into actionable intelligence and positions Rivia as the AI-first platform for clinical trial intelligence. The Role As a Senior AI Engineer at Rivia, you [. .. ]
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Häufig gestellte Fragen
Wieviele offene Stellenangebote gibt es für Drug Monitoring Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 129 offene Stellenanzeigen für Drug Monitoring Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Drug Monitoring Jobs?
Aktuell suchen 19 Unternehmen nach Bewerbern für Drug Monitoring Jobs.
Welche Unternehmen suchen nach Bewerbern für Drug Monitoring Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Drug Monitoring Stellenangebote:
- Tigermed (28 Jobs)
- Novartis (2 Jobs)
- Roche (2 Jobs)
- Lonza (2 Jobs)
- Astra Zeneca (1 Job)
- Paul- Ehrlich- Institut (1 Job)
In welchen Bundesländern werden die meisten Drug Monitoring Jobs angeboten?
Die meisten Stellenanzeigen für Drug Monitoring Jobs werden derzeit in Niedersachsen (10 Jobs), Berlin (9 Jobs) und Bayern (8 Jobs) angeboten.
