9 Jobs für Clinical Trial Associate
Stellenangebote Clinical Trial Associate Jobs
Job vor 4 Tagen bei StepStone gefunden
Randstad Deutschland GmbH Co. KG
• München Muenchen
Angebote von Zeitarbeitsunternehmen
Weihnachtsgeld 30+ Urlaubstage
[. .. ] sich jetzt und in kürzester Zeit bringen wir Sie Ihrem Traumjob ein Stück näher. Wir legen Wert auf Chancengleichheit und begrüßen die Bewerbung von Menschen mit Behinderung. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Aufgaben Unterstützung des Clinical-Trial-Associate-bzw. des Contracting-Teams im Bereich der klinischen Forschung als Trial Support Kontinuierliche Verwaltung und Archivierung von Studiendokumenten und deren Administration Unterstützung bei der Erstellung von Studienunterlagen sowie Dokumenten zur Ethik- und Behörden-Einreichung Vertragsadministration in den einzelnen Indikationen Distribution von Studienmaterialien und allgemeine Dateneingabe Unterstützung im Bereich Contracting rund [. .. ]
Job vor 7 Tagen bei StepStone gefunden
Randstad Deutschland GmbH Co. KG
BTA (m/w/d)
• Mannheim
Angebote von Zeitarbeitsunternehmen
Betriebliche Altersvorsorge
[. .. ] und bewerben Sie sich direkt online. Wir garantieren eine individuelle Beratung, persönliche Betreuung und effiziente Bearbeitung Ihrer Bewerbung. Menschen mit einem Handicap sind bei uns herzlich willkommen. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Aufgaben Unterstützung des Clinical-Trial-Associate-und/oder des Contracting-Teams als Trial Support im Bereich der klinischen Forschung Unterstützung bei der Erstellung von Studienunterlagen und Dokumenten zur Ethik- und Behörden-Einreichung Kontinuierliche Verwaltung und Archivierung von Studiendokumenten und deren Administration Unterstützung der Administration im Bereich Contracting rund um erstellte Studienverträge (Tracking, Versand, Qualitätskontrolle, Archivierung) Vertragsadministration [. .. ]
Job vor 7 Tagen bei StepStone gefunden
Randstad Deutschland GmbH Co. KG
BTA (m/w/d)
• Holzkirchen, Oberbayern Holzkirchen;Landkreis Miesbach
Angebote von Zeitarbeitsunternehmen
Weihnachtsgeld 30+ Urlaubstage
[. .. ] Ziel Bewerben Sie sich jetzt direkt online Wir legen Wert auf Chancengleichheit und begrüßen die Bewerbung von Menschen mit Behinderung, deren Inklusion uns ein besonderes Anliegen ist. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Aufgaben Unterstützung des Clinical-Trial-Associate-bzw. des Contracting-Teams im Bereich der klinischen Forschung als Trial Support Kontinuierliche Verwaltung und Archivierung von Studiendokumenten sowie deren Administration Unterstützung bei der Erstellung von Studienunterlagen und Dokumenten zur Ethik- und Behörden-Einreichung Vertragsadministration in den einzelnen Indikationen Distribution von Studienmaterialien sowie allgemeine Dateneingabe Unterstützung im Bereich Contracting rund [. .. ]
Job vor 2 Tagen bei StepStone gefunden
Astra Zeneca
• München Muenchen
Führungs-/ Leitungspositionen
Do you thrive at the intersection of AI innovation and
clinical translation? Do you have expertise in, and a passion for leading cross functional teams to drive innovation? Would you [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] like to apply your expertise to impact the Oncology and/or Bio Pharma strategic vision in a company that follows the science and turns ideas into life changing medicines? Then Astra [. .. ] decisions. Working knowledge of AI and machine learning methodologies applicable to biomarker discovery, including supervised learning, foundation models, multimodal approaches, and emerging AI technologies. Understanding of biomarker development pathways, clinical trial design, and translational research strategies across different stages of drug development. Strong communication, presentation, and influencing skills, with the ability to effectively engage scientific and clinical stakeholders and communicate complex concepts to diverse audiences. Demonstrated ability to balance scientific innovation with pragmatic execution, delivering high-quality outputs in a fast-[. .. ] agile work A diverse, inclusive, and bias-free work environment, actively welcoming applications from all qualified candidates, regardless of background or characteristics JBRT1DE. Astra Zeneca sucht in München eine/n Associate Director (m/f/d) , Computational Pathology Biomarker Lead (Oncology/ Bio Pharma) (ID-Nummer: 14359282) 00856606 [. .. ]
Job vor 2 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 [. .. ]
Job am 23.07.2026 bei Mindmatch.ai gefunden
F. Hoffmann- La Roche AG
• AT- 2 Schweiz
Führungs-/ Leitungspositionen
[. .. ] our medicines, define how to manage risks to patients, and coordinate the pharmacovigilance system activities for the company, ensuring a safe journey for every individual patient, everywhere. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Responsibilities Provide essential clinical safety and pharmacovigilance support across the entire Roche portfolio, influencing both early and latephase development activities. Act as a key member of the safety team, offering crucial safety oversight and input into all aspects of study management from development through postmarket. Lead critical postmarket safety activities, including signal evaluation, benefitrisk [. .. ] personal and professional development. Qualifications Relevant postgraduate qualification (Ph D, MSc, medical degree, Pharm D, or other postgraduate health professional qualifications) . Strong understanding of Gx P, regulated processes, and the endtoend clinical trial lifecycle. Excellent communication skills, written and verbal, capable of effectively collaborating with remote partners on a global team. Adept at applying complex data analysis and statistical methods to evaluate, interpret, and present scientific data with clarity. Strong presentation skills, effective at summarizing and presenting key considerations and decision points to [. .. ]
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 [. .. ] Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations. Ensures all country and site level trial essential documents required by ICHGCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction) . Sets up and maintains the [. .. ]
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 [. .. ] Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant Sponsor SOPs and local regulations. Ensures all country and site level trial essential documents required by ICHGCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with Sponsor SOPs. Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction) . Sets up and maintains the [. .. ]
Job vor 2 Tagen bei Neuvoo.com gefunden
IQVIA
Führungs-/ Leitungspositionen
Job Overview The
Associate Medical Director will provide medical,
clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities. Essential Functions Medical Monitoring Primarily serves as Global Medical Advisor on [. .. ] (IDB) , and/or Case Report Forms (CRFs) . Provides therapeutic area/ indication training for the project clinical team. Attends and presents at Investigator Meetings. Performs review and clarification of trial-related Adverse Events (AEs) . May perform medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. May provide medical support for the Analysis of Similar Events (AOSE) , in collaboration with or on behalf of Pharmacovigilance [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Associate pro Jahr?
Als Clinical Trial Associate verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 9 offene Stellenanzeigen für Clinical Trial Associate Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Associate Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Trial Associate Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Associate Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Associate Stellenangebote:
- Randstad Deutschland GmbH Co. KG (3 Jobs)
- IQVIA Argentina (2 Jobs)
- Astra Zeneca (1 Job)
- F. Hoffmann- La Roche AG (1 Job)
- IQVIA (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Associate Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Associate Jobs werden derzeit in Bayern (3 Jobs), Baden-Württemberg (1 Jobs) und Schleswig-Holstein (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Associate Jobs?
Clinical Trial Associate Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
