79 Jobs für Clinical Trial Specialist
Stellenangebote Clinical Trial Specialist Jobs
Job am 03.06.2026 bei Neuvoo gefunden
Aktiv Personal- Service GmbH- Biberach an der Riß
• Biberach, Baden- Württemberg
Angebote von Zeitarbeitsunternehmen
Weihnachtsgeld 30+ Urlaubstage Tarifvertrag Vermögenswirksame Leistungen
[. .. ] Riß Vertragsart Vollzeit Arbeitszeit 37, 5 pro Woche Für unseren Kunden, ein innovatives und forschendes Pharmaunternehmen mit Sitz in Biberach, suchen wir eine einen Packaging Labeling Specialist, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical Supply Specialist, Clinical Trial Specialist, Clinical Supply Chain Specialist, Projektmanager Packaging Labeling, Clinical Supply Project Specialist, Clinical Packaging Specialist, Specialist Clinical Operations, Specialist Clinical Development, Spezialist Verpackung und Etikettierung, Spezialist klinische Studien, Spezialist Prüfpräparate, Pharma-Projektmanager oder Life Science Specialist (m/w/d) in Vollzeit Referenznummer AK2026-1162 Aufgaben, Kompetenzen und Verantwortung Ihre Tätigkeiten als [. .. ]
Neu Job vor 3 Std. bei Neuvoo.com gefunden
Medizintechnik Karriere
Field Clinical Specialist Münster-Hannover
• Lower Saxony Hanover
[. .. ] life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. Its our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. The goal will be to help make each site independent on procedures, product preparation and support. Field Clinical [. .. ] reach expert proficiency and deliver positive patient outcomes. This role will collaborate with multiple departments including Sales, Clinical Affairs, Marketing, Quality, Regulatory, and Education. After extensive training, a Field Clinical Specialist will travel frequently within an assigned territory, clinically training customers on the THV technology. Territory: Germany (Bielefeld, Münster, Hannover) Aufgaben How you will make an impact: Working independently in the areas of valve crimping, case management, pre-case planning, post-case management, 3 Mensio management, Therapy Awareness program management and [. .. ] physicians and staff to reach expert proficiency in the THV procedure to deliver positive patient outcomes Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP Responsible for certification of the centers, physicians and other related staff, as well as EW personnel and as outlined within EW SOP Validate software and hardware updates in the field as applicable Regularly reviews clinical support activities, changes in the market and assigned accounts, as [. .. ]
Job gestern bei Jooble gefunden
Office Events P B GmbH
• Biberach an der Riß
Project Office
Specialist (m/f/d) Global Quality
Clinical Supply Biberach, Germany Hybrid Full-time Temporary Assignment (18 months) For our international client in the pharmaceutical industry, we are looking for a Project [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Office Specialist (m/f/d) to support the Global Quality, Devices IMP Delivery environment at the Biberach site starting June 1st, 2026. This position is offered [. .. ] operations and supply chain activities Support budgeting, resource planning, monitoring and reporting processes Act as key user for planning tools including user support and training activities Support operational project activities, trial management and clinical supply chain processes Your Profile Bachelors or Masters degree in Life Sciences, Engineering or a related field Several years of relevant experience within the pharmaceutical industry Experience in planning, supply chain or global operations environments Knowledge of international pharmaceutical regulations (EU/ US) Strong Power BI and reporting [. .. ]
Job gestern bei Jooble gefunden
Barrington James
Clinical Trial Liaison
• Deutschland
Homeoffice möglich
Clinical Science Liaison Manager Location: Germany (Remote/ Home Office) Employment Type: Permanent, Full-Time About the Opportunity An innovative and growing international healthcare company is seeking a Clinical Science Liaison Manager [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to join its Medical Affairs team. The organization specializes in advanced therapies for wound care and skin health and is [. .. ] Engineering, Healthcare Sciences, or a related discipline. Additional clinical or scientific qualifications are advantageous. Experience Minimum 5 years of experience in Medical Affairs, Clinical Science Liaison, Medical Science Liaison, Clinical Specialist, or a related field-based scientific role. Experience within wound care, dermatology, medical devices, pharmaceuticals, or related therapeutic areas is highly desirable. Demonstrated experience engaging with healthcare professionals and key opinion leaders. Skills Competencies Strong scientific and clinical acumen. Excellent presentation and communication skills. Ability to communicate effectively with both [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
Führungs-/ Leitungspositionen
Syneos Health in Vienna is seeking a Global Senior Project
Specialist to ensure excellence in
clinical trial execution. Responsibilities include maintaining project files, effective communication among stakeholders, and supporting quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assurance activities. The ideal candidate will possess an Associates Degree in a relevant field and demonstrate strong organizational, communication, and MS Office skills. Proficiency in English and the ability to work independently are required. The position involves [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Syneos Health
Sr Project Specialist
• AT- 9 Wien
25108671 Global Senior Project
Specialist (Sponsor Dedicated) Germany Syneos Health is a leading fullyintegrated life sciences services organization built to accelerate customer success. We partner with innovators at every point [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Job Responsibilities Setup, maintain and/or close out project files and study information (e. g. , regulatory documents, Trial Master File (TMF) , enrollment, Adverse Events (AE) / Serious Adverse Events (SAE) , site supplies, Institutional Review Board reapprovals, data queries) on a variety of databases and systems. Attend, participate, prepare and distribute meeting minutes and action items for both internal and external meetings (sponsor, trusted process, functional, investigator [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Probando
• AT- 9 Wien
Probando is a healthtech company dedicated to accelerating medical breakthroughs by connecting the right patients with
clinical studies. Active since 2020, we have already successfully completed over 400 projects and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expanded operations across 21 countries. Digital marketing is at the core of our patient recruitment strategy. We bridge the gap between complex medical protocols and humancentric marketing. If you are a datadriven marketer who wants their campaigns [. .. ] As Performance Marketing Manager, you will take ownership of our digital marketing budget and acquisition strategy. You will work handinhand with our specialized international Study Nurses, who translate rigid clinical trial protocols into compliant, patientfriendly content. Your job is to take their expert input and turn it into highperforming paid campaigns (Meta, Google, other digital channels) by optimizing targeting, budget allocation, and funnel conversion. Responsibilities Campaign management: strategy, setup, and daytoday optimization of paid campaigns across Meta (Facebook/ Instagram) and Google [. .. ]
Job am 31.05.2026 bei Mindmatch.ai gefunden
IQVIA
Global Clinical Contracts Lead
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and [. .. ] negotiator. Equivalent combination of education, training and experience. Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug development process. Knowledge and ability to apply GCP/ ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and companys Corporate Standards. Strong understanding of particular Sponsor or stakeholder need and ability to share this knowledge effectively with others. Ability to utilize metrics and [. .. ]
Job am 29.05.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
[. .. ] stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and [. .. ] negotiator. Equivalent combination of education, training and experience. Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug development process. Knowledge and ability to apply GCP/ ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and companys Corporate Standards. Strong understanding of particular Sponsor or stakeholder need and ability to share this knowledge effectively with others. Ability to utilize metrics and [. .. ]
Job am 28.05.2026 bei Mindmatch.ai gefunden
CBmed GmbH
Senior Immunoassay Scientist ELISA/ ECLIA Expert
• AT- 6 Graz
A biomarker research center in Graz is seeking a Senior Immunoassay
Specialist to develop and validate protocols for immune assays. The ideal candidate will have extensive experience with ELISA [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and ECLIA assays, and a robust foundation in clinical trial support and sample analysis. Applicants are required to hold at least a MSc in a related field. This position offers a full-time unlimited contract with a competitive salary of 69, 060 per year. J-18808-Ljbffr 92871350 [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
[. .. ] stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements. Report contracting performance metrics and out of scope contracting activities as required. Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and [. .. ] or clinical research organization clinical site contracting experience Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug development process. Good understanding of clinical trial contract management. Fluent in English and German language IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
IQVIA Argentina
Contract Negotiator
• AT- 9 Wien
[. .. ] stakeholders, and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and [. .. ] regional experience acting as a contract negotiator. Good negotiating and communication skills with the ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of the drug development process. Knowledge of and ability to apply GCP/ ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, SOPs and the companys Corporate Standards. Strong understanding of particular sponsor or stakeholder needs and the ability to share this knowledge effectively with others. Ability [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] Senior/ Medical Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] their clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] on medical issuesproviding clear, informed guidance and answering complex questions related to medical, legal, and regulatory concerns. Responsibilities Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical [. .. ] safety-related documentation. Team Client Engagement: Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications: Medical Doctor (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise: Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge: Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation, and internal SOPs. Adaptability: Comfortable working in fast-paced environments with [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
Backend Platform Engineer (Rust) - Digital Health
• Berlin
[. .. ] facilities across Germany, MEDIAN offers a dynamic and innovative environment for employees across a wide range of professional and service areas, with diverse opportunities for entry and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] development. As a specialist in rehabilitation and reintegration, we support our patients on their path to recovery and their return to everyday life fully in line with our guiding principle: Live your life. Your main tasks Were building a new MVP to extend our rehabilitation aftercare platform, and youll be part of the backend crew. As such, you will work closely with other backend, web, mobile, QA and Dev (Sec) Ops engineers, as well as Product Managers, UX designers, Rollout team and clinical trial management. The main focus is the go-to-market of the MVP to extend our existing product lines within the guardrails of ISO 27001, ISO 27701, GDPR and C5 (including post-quantum strategies) . A big part of the work will also include the uplifting of a handful of (well-[. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Lachen, Schwyz
Octapharma AG in Lachen, Switzerland, is seeking a
Clinical Trial Manager to oversee the integrity of clinical data across multiple studies. The role demands strong analytical abilities to ensure compliance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and improve therapeutic options while working closely with various functional teams. As part of a family-oriented organization, youll have the chance to make a meaningful impact in advancing human [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Backend Platform Engineer (Rust) - Digital Health
• Berlin
[. .. ] facilities across Germany, MEDIAN offers a dynamic and innovative environment for employees across a wide range of professional and service areas, with diverse opportunities for entry and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] development. As a specialist in rehabilitation and reintegration, we support our patients on their path to recovery and their return to everyday life fully in line with our guiding principle: Live your life. Your main tasks Were building a new MVP to extend our rehabilitation aftercare platform, and youll be part of the backend crew. As such, you will work closely with other backend, web, mobile, QA and Dev (Sec) Ops engineers, as well as Product Managers, UX designers, Rollout team and clinical trial management. The main focus is the go-to-market of the MVP to extend our existing product lines within the guardrails of ISO 27001, ISO 27701, GDPR and C5 (including post-quantum strategies) . A big part of the work will also include the uplifting of a handful of (well-[. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
[. .. ] countries are dedicated to this mission. Would you like to become part of our success story? Join Merz Aesthetics The following responsibilities are awaiting you: You plan [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and perform various Clinical medical devices medicinal products project audits against Gx P and local regulatory requirements. You create audit plans for the studies, based on risk assessments/ analyses, as well as plan and perform internal process and vendor audits. You lead the evaluation and management of clinical site-specific escalations related to persistent or [. .. ] have prior experience developing risk-based quality management programs across clinical development. You have first experience working and communicating within cross-functional and international teams. You understand the overall clinical trial management process, including the protocol and other clinical trial-related plans and documents. You have critical thinking and analytical skills to understand and analyze complex data and provide insight into risk reports, trends, and outliers in data. You have comprehensive knowledge of the regulations and standards for conducting clinical trials [. .. ] Ongoing training: Your personal and professional development is the key to success for us. To foster this, we conduct regular development discussions and facilitate a wide range of management and specialist training courses, soft skills courses, e-learning courses, language courses and coaching sessions. Find out more about our benefits at https:/ / careers. merz-aesthetics. com. We look forward to your application #J-18808-Ljbffr 96199523 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Clinical Research Associate
Job Title: Field
Clinical Research Associate This role supports the Clinical Operations team by overseeing clinical studies, ensuring high-quality human study data collection, and facilitating collaboration between internal study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams, contract research organizations, and clinical sites. You will take ownership of site monitoring and study oversight for multiple clinical studies, with a focus [. .. ] study protocols, Good Clinical Practice (GCP) , and ICH guidelines. Collaborate closely with contract research organizations and university sites to facilitate training of site and vendor personnel and support clinical trial execution. Track and maintain regulatory documentation and ensure that all required records are complete, accurate, and up to date. Work with incoming study data to reconcile data reports, identify discrepancies, and generate reports for invoicing and other operational needs. Resolve data queries and delinquencies in a timely manner, coordinating with [. .. ] research organization or in a sponsor role supporting clinical studies. Experience in clinical operations, clinical trial execution, or field clinical roles such as Field Clinical Research Manager or Field Clinical Specialist. Exposure to health technologies and medical devices, especially wearable technology. Comfort working with spreadsheets and data tracking tools to manage project and study information. Experience navigating multiple concurrent projects and coordinating across crossfunctional teams. Ability to interact professionally with leadership and external partners, representing the clinical operations function effectively. Strong [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Social Media Marketing Specialist
• Wien
Probando is a healthtech company dedicated to accelerating medical breakthroughs by connecting the right patients with
clinical studies. Active since 2020, we have already successfully completed over 400 projects [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and expanded operations across 21 countries. Digital marketing is at the core of our patient recruitment strategy. We bridge the gap between complex medical protocols and humancentric marketing. If you are a datadriven marketer who wants their campaigns [. .. ] As Performance Marketing Manager, you will take ownership of our digital marketing budget and acquisition strategy. You will work handinhand with our specialized international Study Nurses, who translate rigid clinical trial protocols into compliant, patientfriendly content. Your job is to take their expert input and turn it into highperforming paid campaigns (Meta, Google, other digital channels) by optimizing targeting, budget allocation, and funnel conversion. Responsibilities Campaign management: strategy, setup, and daytoday optimization of paid campaigns across Meta (Facebook/ Instagram) and Google [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
W2 Professorship in Surgical Oncology
• Gießen, Hessen
[. .. ] within the Clinic for General, Visceral, Thoracic and Transplant Surgery in research, teaching, and patient care across the entire spectrum, and will further develop this field through [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] modern approaches in clinical and translational research. Your clinical work will cover visceral and thoracic surgery, including laparoscopic, thoracoscopic, and robotic procedures. You will be expected to initiate and coordinate clinical projects and studies through the Giessen branch of the Marburg Coordinating Center for Clinical Trials (KKS) and the Surgical Center for Clinical Trials [. .. ] ) . With the establishment of the professorship, you will also actively participate in expanding the study infrastructure through cooperation and integration into existing networks, such as the crosssite surgical trial network CHIRNet, as well as regionally important networks, such as the University Colorectal Center of Central Hessen (UDM) . In collaboration with the general, visceral, thoracic, and transplantation surgery at the UKGM Marburg site, you will primarily contribute to the establishment of the Comprehensive Cancer Center (CCC) Frankfurt Giessen Marburg [. .. ] renowned national and international journals) are required. Experience in coordinating scientific projects within interdisciplinary networks and success in the independent acquisition of external funding are also required. Proof of a specialist qualification (board certification) in general or visceral surgery is required, as well as experience in minimally invasive (robotic) surgery. A specialization in oncological visceral surgery is also required, which can be demonstrated by designations such as Specialized Visceral Surgery, the Surgical Oncology EBSQ Examination, or certification as a boardcertified specialist [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Nurse Wound Care Specialist
• Hamburg
Title: Freelance
Clinical Trial Nurse, ICW Certified Region: Hamburg (home-based/field role) Employment Type: Contract FTE: 0-50 Home Visit Rate: 90 EUR Per Home Visit (Typically 1 hour) Overview We [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] are seeking an experienced Wound Care Nurse to support a Phase 2 clinical study evaluating a novel treatment for chronic wounds. This [. .. ] data quality Liaise closely with investigators, study coordinators, and project teams Provide a high standard of patient care, support, and communication Requirements Qualified Registered Nurse (or equivalent) Certified Wound Care Specialist (ICW) or equivalent qualification Strong experience in chronic wound management and advanced wound care Confident performing: wound assessments dressing changes sample collection clinical documentation Ability to work independently in a homecare setting Excellent attention to detail and protocol adherence Fluent German language skills Willingness to complete GCP and study-specific [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
PLM Specialist (m/w/d)
• Biberach an der Riß, Baden- Württemberg
Homeoffice möglich
Betriebliche Altersvorsorge Weihnachtsgeld 30+ Urlaubstage Vermögenswirksame Leistungen
[. .. ] Std. / Woche) Vergütung: 5.622, 00 EUR brutto/ Monat zzgl. variabler, leistungsorientierter Prämie Für wen suchen wir Wir suchen für unseren Kunden, einem international agierenden Industrieunternehmen in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Biberach, einen PLM Specialist (m/w/d) in Vollzeit. Das bringen Sie mit Abgeschlossenes Masterstudium im naturwissenschaftlichen Bereich (z. B. Life Sciences, Biowissenschaften, Chemie, Biotechnologie, Pharmazie oder vergleichbare Studiengänge) sowie erste Berufserfahrung in der Pharmaindustrie oder einer regulierten Branche Erfahrung in der Pharmaindustrie, insbesondere im Bereich klinische Versorgung, Verpackung und Kennzeichnung von Vorteil Kenntnisse [. .. ] treiben kontinuierliche Verbesserungen voran Sie prüfen die Herstell- und Chargendokumentation externer Lohnhersteller und stellen die Einhaltung von Zeit-, Qualitäts- und Budgetvorgaben sicher Sie vertreten Verpackungs- und Etikettierungsthemen in globalen Clinical Trial Teams und unterstützen die Studienumsetzung Sie bearbeiten und bewerten Abweichungen sowie deren Ursachenanalysen und Maßnahmenverfolgung Vorteile attraktives Gehalt von 5.622 EUR brutto/ Monat persönliche und wertschätzende Betreuung durch unsere Niederlassung bis zu 30 Tage Urlaub Urlaubs- und Weihnachtsgeld flexibles Gleitzeitkonto betriebliche Altersvorsorge und vermögenswirksame Leistungen 150 Euro Prämie bei [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
W2 Professorship in Surgical Oncology
• Gießen, Hessen
[. .. ] within the Clinic for General, Visceral, Thoracic and Transplant Surgery in research, teaching, and patient care across the entire spectrum, and will further develop this field through [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] modern approaches in clinical and translational research. Your clinical work will cover the fields of visceral and thoracic surgery, including laparoscopic, thoracoscopic, and robotic procedures. You will be expected to initiate and coordinate clinical projects and studies through the Giessen branch of the Marburg Coordinating Center for Clinical Trials (KKS) and the Surgical Center [. .. ] consortium) . With the establishment of the professorship, you will also actively participate in expanding the study infrastructure through cooperation and integration into existing networks, such as the crosssite surgical trial network CHIRNet, but also into regionally important networks, such as the University Colorectal Center of Central Hessen (UDM) . Alongside a close cooperation with the general, visceral, thoracic, and transplantation surgery of the UKGM at the Marburg site, you will primarily bring your expertise into the establishment of the Comprehensive [. .. ] journals) are required. You should also have experience in coordinating scientific projects within interdisciplinary networks, as well as demonstrate success in the independent acquisition of external funding. Proof of a specialist qualification (board certification) in general or visceral surgery is required, as well as experience in minimally invasive (robotic) surgery. Furthermore, you should have a specialization in the field of oncological visceral surgery. This specialization can be demonstrated, for example, by the additional designation Specialized Visceral Surgery, the Surgical Oncology EBSQ [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Senior Global Medical Manager Obesity Liver Health
• Ingelheim am Rhein, Rheinland- Pfalz
[. .. ] at the forefront of scientific storytelling and insights integration, translating deep scientific knowledge into strategic actions that resonate across internal teams and external experts. Collaborating closely with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the innovation and clinical development teams, focus markets, regional teams, and crossfunctional global stakeholders, you will ensure alignment, impact, and excellence in medical affairs. Tasks Responsibilities Lead the development and execution of globally aligned medical strategies for the Obesity and Liver Health pipeline, ensuring adaptation to evolving scientific, regulatory, and market dynamics Cocreate integrated [. .. ] integrate actionable insights into strategic decisions Build globallocal Medical Affairs collaborations to ensure knowledge transfer, launch readiness, and regional alignment Requirements Medical Doctor (e. g. , endocrinologist, internal medicine, obesity specialist, primary care physician) with a specialty in obesity medicine and experience in Obesity and Liver Health Longterm experience in the pharmaceutical industry, including several years in Medical Affairs as a Medical Advisor or Medical Manager in a global or international role Deep understanding of drug development, clinical trial design, data analysis, and interpretation, with expertise in introducing new medicines or expanding indications at a global level (e. g. , Obesity, Liver, or Cardiometabolic Health) Strategic thinker with strong crossfunctional collaboration skills, a clear understanding of medicomarketing processes, and the ability to lead impactful crossregional medical initiatives Indepth knowledge [. .. ]
Job am 03.06.2026 bei Jobleads gefunden
Director, Computational Pathology Biomarker Lead (Oncology/ Bio Pharma) (m/f/d)
• München, Bayern
Führungs-/ Leitungspositionen
Director, Computational Pathology Biomarker Lead (Oncology/ Bio Pharma) (m/f/d) Do you thrive at the intersection of AI innovation and
clinical translation? Do you have expertise in, and a passion [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for leading cross functional teams to drive innovation? Would you 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 [. .. ] in AI-powered biomarker development by establishing quantitative composite scores, disease progression trajectory models, spatial biomarker signatures, and novel metrics from images that capture organ-specific pathology patterns and enable trial enrichment, patient stratification, and alternative endpoint strategies that accelerate clinical timelines. Develop strategic approaches for reusable biomarker platforms that function as platform assets across multiple indications sharing common biological mechanisms, traveling with biological pathways across disease continuums. Establish analytical and clinical validation frameworks for multimodal biomarkers with strategic emphasis on [. .. ] pathways across Oncology and/or Bio Pharmaceuticals programs. Proven communication, presentation, and influencing skills at senior leadership levels with ability to articulate AI value proposition and implementation strategies to both specialist and non-specialist audiences. Outstanding analytical, research, and organizational skills with excellent problem-solving capabilities, clear understanding of the balance between innovation, smart risk-taking, fit-for-purpose solutions, and timely project delivery, and track record of consistent delivery and impact on drug development programs through AI innovation and successful [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Specialist pro Jahr?
Als Clinical Trial Specialist verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 79 offene Stellenanzeigen für Clinical Trial Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Specialist Jobs?
Aktuell suchen 28 Unternehmen nach Bewerbern für Clinical Trial Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Specialist Stellenangebote:
- IQVIA (9 Jobs)
- Intuitive (5 Jobs)
- Abbott (4 Jobs)
- Office Events Wiesbaden (3 Jobs)
- Astra Zeneca (3 Jobs)
- Edwards Lifesciences (3 Jobs)
In welchen Bundesländern werden die meisten Clinical Trial Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Specialist Jobs werden derzeit in Baden-Württemberg (13 Jobs), Hessen (10 Jobs) und Niedersachsen (9 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Specialist Jobs?
Clinical Trial Specialist Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
