5 Jobs für Clinical Trials Associate
Stellenangebote Clinical Trials Associate Jobs
Job vor 14 Tagen bei StepStone gefunden
Universitätsklinikum Carl Gustav Carus Dresden
• Dresden
Teilzeit
Jobticket Work-Life-Balance
[. .. ] Space (BMFTR) that aims to develop generalizable, clinically relevant AI approaches for surgical video analysis, working with one of the worlds largest prospective surgical video registries. As [...]
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[...] a Postdoctoral Research Associate, you will contribute to evaluating and optimizing the real-world performance of state-of-the-art AI models for surgical video understanding. The position is embedded in an interdisciplinary and international research environment within the Surgical Artificial Intelligence research group led by Dr. Fiona Kolbinger, which is jointly affiliated with the Department of Visceral, Thoracic and Vascular Surgery and the Else Kröner Fresenius Center for Digital Health at TU Dresden. The group works at the intersection of AI development, clinical surgery, and translational research, with the goal of developing and clinically evaluating AI tools that improve surgical care. Aufgaben Design and lead research projects on AI for surgical video understanding, including vision-language model benchmarking and optimization, clinical translation (early-stage clinical feasibility studies and randomized controlled trials) , and human-AI interaction in surgery Collaborate with national and international partners Mentor graduate and undergraduate student researchers within the group Prepare journal publications and presentations at national and international conferences Contribute to grant writing and scientific dissemination Profil Doctoral degree in computer science, biomedical engineering, electrical/ computer engineering, [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Biogen, Inc.
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
Associate Director, Country Site Operations FSP Oversight Manager Applyremote type: Hybridlocations: Baar, Switzerlandtime type: Full timeposted on: Posted Todayjob requisition id: REQ23832For our offices in Baar we are recruiting for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Associate Director, Country Site Operations FSP Oversight Manager About This Role: As the Associate Director, Country Site Operations Functional Service [. .. ] leadership and cross-functional stakeholders to drive and manage the CSOs FSP insourcing model. This role is crucial in overseeing and developing FSP staff who support country-and site-facing clinical trial execution, ensuring the embedding of consistent, efficient processes across regions and therapeutic areas. Your work will ensure alignment with CSOs internal and external stakeholders on FSP role execution, performance, quality, and delivery expectations. Additionally, you will contribute to shaping CSO operational strategy and continuous improvement as part of the CSO extended leadership model. Through varied responsibilities, you will have the opportunity to impact the execution of clinical trials and support the broader strategic goals of the business. What Youll Do: Manage up to 20-25 FSP staff assigned across the clinical portfolio to support CSOs country-and site-level operational objectives. Lead resource forecasting, assignment, and prioritization to support regional delivery needs, portfolio demand, and annual operating plan [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Bristol- Myers Squibb
• AT- 2 Schweiz
Associate Stability Scientist Boudry-CH Find out how well you match with this job Working with Us Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But [...]
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[...] working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. [. .. ] integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-[. .. ]
Job am 09.07.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines complying [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local Study Associate Director is responsible to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived. MAIN RESPONSIBILITIES Has the overall responsibility for the study commitments within the country [. .. ] Affairsled or Academicled studies) . Good knowledge of international guidelines ICH GCP as well as relevant local regulations. Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas. Good knowledge of the Drug Development Process. Excellent understanding of the Clinical Study Process including monitoring. Very good understanding of the Study Drug Handling Process and [. .. ]
Job am 09.07.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
• AT- 9 Wien
Führungs-/ Leitungspositionen
Vienna, Austria Full time Home-based R1546726 To lead Local Study Teams (LSTs) at country level to deliver committed components of
clinical studies according to agreed resources, budget and timelines complying [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with Sponsor Procedural Documents, international guidelines such as ICHGCP as well as relevant local regulations. In addition to leading LST (s) , the Local Study Associate Director may perform site monitoring as needed to support the flexible capacity model. The Local Study Associate Director is responsible to ensure that sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived. MAIN RESPONSIBILITIES Has the overall responsibility for the study commitments within the country [. .. ] Affairsled or Academicled studies) . Good knowledge of international guidelines ICH GCP as well as relevant local regulations. Proven ability to lead and motivate cross functional teams to deliver clinical trials according to or ahead of time plan, budget and with required quality. Good medical knowledge of Oncology, Rare Diseases, cardiology, hematology, CVRM Therapeutic Areas. Good knowledge of the Drug Development Process. Excellent understanding of the Clinical Study Process including monitoring. Very good understanding of the Study Drug Handling Process and [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Associate pro Jahr?
Als Clinical Trials Associate verdient man zwischen EUR 40.000,- bis EUR 60.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 5 offene Stellenanzeigen für Clinical Trials Associate Jobs.
In welchen Bundesländern werden die meisten Clinical Trials Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Associate Jobs werden derzeit in Sachsen (1 Jobs), Schleswig-Holstein (0 Jobs) und Thüringen (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Associate Jobs?
Clinical Trials Associate Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
