Clinical Trials Specialist Stellenangebote

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Stellenangebote Clinical Trials Specialist Jobs bei Stellen-Online

Job vor 14 Tagen gefunden Miltenyi Biomedicine GmbH

IMP Manager- Clinical Trials (m f d) - Homeoffice, Vollzeit

• 51429, Bergisch Gladbach, 51429 Homeoffice möglich

MEHR

Company Description Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life- threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult- to- treat hematological cancers using CAR- T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR T- cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to market and ensuring the safety of [...] mobile work. Exciting opportunities in the development of technologies with a secure future. Cross- border intercultural cooperation and short communication channels A collegial corporate culture and flexible working hours enable time management on your own terms Personalized employee development program: specialist and personal training courses provided by our own Miltenyi University Diverse corporate benefits with regard to employee health, and staff [...]
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Stellenangebote Clinical Trials Specialist Jobs bei StepStone

Neu Job vor 11 Std. gefunden ZEISS Regulatory/ Clinical Affairs (RA/ CA) Team Lead (m/f/x) • Jena Führungs-/ Leitungspositionen Beratungs-/ Consultingtätigkeiten

MEHR

[...] to function optimally. Medical technology from ZEISS supports medical professionals in improving the lives of patients worldwide. The fact that our actions have a direct impact on peoples well- being is what drives us every day. Your Role You are specialist and disciplinary manager of the Regulatory and Clinical Affairs department of one or more product lines in the respective division (BS) You are overseeing a team with an [...] the product line, implementing for the Regulatory Affairs Lifecycle or Clinical Affairs (Clinical Evaluation and Strategy) You are supporting the further development of the department, effectively enhancing expertise by introducing innovative concepts for the design and implementation of (global) clinical trials. You are fostering collaboration with interface departments and guarantee increased value to our specialty department. Completed natural science or technical [...]
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Stellenangebot Clinical Trials Specialist Job bei Merz Aesthetics

Job vor 8 Tagen gefunden Merz Aesthetics

Field Clinical Specialist Gebiet: West Deutschland (m/w/d) in Teilzeit

• Westdeutschland Beratungs-/ Consultingtätigkeiten Teilzeit Homeoffice möglich Flexible Arbeitszeiten

MEHR

[...] Raleigh, North Carolina, USA. Tagtäglich setzen wir uns mit mehr als 2. 500 Mitarbeiter innen in 26 Ländern dafür ein, die Schönheit der Haut wiederherzustellen und zu erhalten. Möchtest Du Teil unserer Erfolgsgeschichte werden? Dann starte bei Merz Aesthetics Field Clinical Specialist Gebiet: West Deutschland (m/w/d) in Teilzeit Du kontaktierst Ärzte zur Terminvereinbarung von Trainings, bereitest diese sorgfältig vor, dokumentierst und führst [...] und leitest diese an die entsprechenden internen Abteilungen weiter Als kompetente Ansprechperson kümmerst Du Dich eigenständig um die Beantwortung von Kundenanfragen im Bereich Ästhetik und den damit verbundenen medizinisch- wissenschaftlichen Themen. Zudem übernimmst Du die verantwortungsvolle Betreuung von Investigator Initiated Trials (IITs) , um sicherzustellen, dass alle Projekte erfolgreich umgesetzt werden Du nimmst aktiv an nationalen und internationalen FCS- Meetings sowie [...]
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Jobs aus StepStone

Weitere Stellenangebote Clinical Trials Specialist bei StepStone

Stellenangebot Clinical Trials Specialist Job bei Dr. Falk Pharma GmbH

Job gestern gefunden Dr. Falk Pharma GmbH Medical Writer (m/f/d) • Freiburg Homeoffice möglich

MEHR

[...] as well as patient health and well- being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your main responsibility will be to edit and/ or write regulatory and clinical content and documentation, related to new drugs or clinical trials You will draft and manage regulatory and clinical research healthcare documents, including articles and white papers. In this context you [...] agencies, to compile and organize information and create paperwork that will be reviewed by government or regulatory agencies, such as the EMA or FDA. In this context, you will also be in close contact and exchange with the relevant internal specialist departments. Other responsibilities include conducting extensive research on medical- related topics to ensure that all content is factual and accurate [...]
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Job vor 5 Tagen gefunden Formycon AG

Master Data Specialist (gn) Supply Chain Logistics

• Martinsried/ Planegg Homeoffice möglich

MEHR

[...] an experienced team comprised of around 240 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process. Our focus is on treatments in ophthalmology and immunology as well as for other key [...] privacy regulations desirable Flexible working time Hybrid work 30 days paid vacation Formycon pension Group accident insurance Formycon card Continuing education offers Team spirit, great working atmosphere and much more . Formycon AG sucht in Martinsried/ Planegg eine/n Master Data Specialist (gn) Supply Chain Logistics (ID- Nummer: 11814530) 26702792 [...]
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Job vor 5 Tagen gefunden Formycon AG Senior IT Infrastructure/ IT Operations Specialist (gn) • Martinsried/ Planegg Beratungs-/ Consultingtätigkeiten Homeoffice möglich

MEHR

[...] an experienced team comprised of around 240 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process. Our focus is on treatments in ophthalmology and immunology as well as for other key [...] our IT Operations To support our team in Martinsried near Munich, we are looking for suitable candidates for this full- time and permanent position, to begin work as soon as possible. We are seeking a Senior IT Infrastructure/ IT Operations Specialist (gn) to join the Information and Business Technology (IBT) department with a strong focus on M365 technologies and a commitment [...]

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Stellenangebote Clinical Trials Specialist Jobs bei JobMESH

Job vom 06.12.2024 Miltenyi Biomedicine GmbH

IMP Manager- Clinical Trials (m f d)

• North Rhine- Westphalia

MEHR

Company Description Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life- threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult- to- treat hematological cancers using CAR- T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR T- cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to market and ensuring the safety of [...] mobile work. Exciting opportunities in the development of technologies with a secure future. Cross- border intercultural cooperation and short communication channels A collegial corporate culture and flexible working hours enable time management on your own terms Personalized employee development program: specialist and personal training courses provided by our own Miltenyi University Diverse corporate benefits with regard to employee health, and staff [...]

Stellenangebote Clinical Trials Specialist Jobs bei Neuvoo.com

Stellenangebot Clinical Trials Specialist Job bei ZEISS

Job vor 5 Tagen gefunden ZEISS Regulatory/ Clinical Affairs (RA/ CA) Team Lead (m/f/x) Führungs-/ Leitungspositionen

MEHR

Stellenangebote Clinical Trials Specialist Jobs bei Jobleads

Job vor 2 Tagen gefunden

Clinical Research Associate (m/w/d)

• Jena, Thüringen Work-Life-Balance

MEHR

Clinical Research Associate (m/w/d) Clinical Research We are offering a position in the medical device sector with ambitious and passionate people [...] professional development. Your work will focus on: Planning, preparing, and managing all monitoring- related activities, performance of monitoring of trial/ registry sites If required, assisting in study audits Main line of communication between investigators/ site staff and Occlutech Conducting clinical trials, clinical studies, and registries according to all applicable regulations, commonly accepted practices, and Occlutech s internal guidelines Preparing essential documents [...] and coffee as well as regular team sporting events Ready to apply? We look forward to receiving your application (cover letter and CV) at bewerbung occlutech. com. Only applications in English will be evaluated. About Occlutech Occlutech is a leading specialist provider of minimally invasive cardiac devices, with a mission to improve the quality of life for people with heart conditions. [...]
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Job vor 3 Tagen gefunden Data Transparency Specialist Data Sharing, Anonymisation and Clinical Trial Disclosure (f/m/d. . . • München, Bayern

MEHR

Your responsibilities will include Redaction of clinical trial documents Anonymisation of individual patient data Assessing data sharing requests, reviewing informed consent forms for data sharing feasibility Disclosure [...] development and clinical science Experience in redaction of CCI and PPD in clinical documents Knowledge of EMA policy 0070 is a plus Experience in data anonymization and programming (e. g. , R/ SAS) is a plus Knowledge of the clinical trials disclosure regulatory environment and experience with Clinicaltrials. gov and EudraCT/ CTIS is a plus Experience in medical writing is a [...]

Job vor 3 Tagen gefunden

Clinical Research Associates (all levels) - Germany

• München, Bayern

MEHR

[...] enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life- changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our [...] roles are permanent. The CRA: Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on- site visits to assess protocol and regulatory compliance and manages required documentation. . Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH- GCP guidelines, applicable regulations and SOPs to [...]
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Job vor 9 Tagen gefunden Project Manager Clinical Supply Systems

MEHR

Project Manager Clinical Supply Systems at Clin Choice (View all jobs) Ludwigshafen, Germany Are you interested in working directly for a single sponsor [...] culture. As a client- facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high- trust environment with the client counter- parts. The Freelance Project Manager for Clinical Supply Systems ensures that clinical trials have the necessary supplies on time and in compliance with regulations. Responsibilities include preparing and maintenance of training materials, processing [...] and collection of statistics and KPIs, as well as implementation of ad hoc views, dashboards, unvalidated reports under supervision by the Program Manager Clinical Supplies Systems and external consultants. Development of new local processes and process optimizations with the respective specialist area, from idea to testing to implementation with the support of supervisors. Definition of new local processes within Clinical Supply [...]

Job vor 10 Tagen gefunden

Field Medical Science Liaison- Diabetes (m/w/d)

MEHR

[...] Milliarden US- Dollar, ein Wachstum von 18 gegenüber 2021. Das Unternehmen mit Hauptsitz in San Diego, Kalifornien, und weiteren Niederlassungen in den USA, Europa und im asiatisch- pazifischen Raum beschäftigt weltweit über 9. 000 Mitarbeiter. Position Summary The Field Science Specialist/ Medical Science Liaison acts as a bridge between the company and healthcare professionals (HCPs) , providing in- depth scientific knowledge, [...] and research. The FSS is the medical and scientific expert in the field responsible for engaging with key opinion leaders (KOLs) , facilitating in depth/ sophisticated discussions on the benefit of the use of CGM for patients with Diabetes including clinical data and its optimal use. Your insights will drive our clinical strategy, support product development and enhance our educational activities. [...] of diabetes treatment. Support sales teams with scientific information and updates on current research and clinical practices during product launches, customer meetings and training sessions. Clinical Research Support: Support the clinical research teams to identify sites and investigators for clinical trials. Data Dissemination and Insights: Gather information from KOLs as to how they are using our products. Feedback information to marketing [...]

Job vor 10 Tagen gefunden Clinical Research Associates (experienced) - Germany • München, Bayern

MEHR

Job vom 05.12.2024

Business Development Manager/ Account Executive

• Frankfurt, Hesse Homeoffice möglich

MEHR

[...] stress, higher quality, and shorter hours: Ideals Virtual Data Room : A web- based cloud platform used by companies in a wide range of industries to ensure secure confidential document sharing for online due diligence, fundraising transactions, corporate reporting, licensing, clinical trials, and other business goals. Ideals Board : A cloud platform with web and mobile applications used by board members, CEOs, [...] for each element. Our interview assignments simulate what it s like to work at Ideals and the type of tasks you ll tackle. Here are the stages of the interview process for this role: Screening call with the Talent Acquisition Specialist (up to 30 mins) Hiring Manager interview (up to 45 mins) Presentation Role Play with the Hiring Manager (up to [...]
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Job vom 02.12.2024 Head Medical Safety Operations (m/f/d) • Holzkirchen, Bayern

MEHR

Job Description Summary Designs develops safety surveillance strategy for products and approval. Responsible for the company s drug surveillance program including the necessary follow- up, risk assessment, and relatedness to product on adverse reaction reports, oversight of safety in clinical trials and post marketing programs. Participates in the resolution of any legal liability and complying with governmental regulations. Provides and contributes trending and safety signal detection and risk management assessment for the products life cycle. Provides safety support to the clinical development teams. Your Key Responsibilities: Manages and coaches a team of Medical Safety Experts/ Specialist/ Associates. Manages the strategic planning of the activities delivered by the Medical Safety Experts/ Specialist/ Associates. Provides strategic leadership within [...]

Job vom 23.11.2024

Specialist, Pharmacovigilance

• Mannheim, Baden- Württemberg

MEHR

[...] challenges and opportunities? Then, Pharmalex is your career opportunity. Pharmalex is one of the leading service companies for the Pharmaceutical Industry globally and is specialized in all aspects of drugs and medical devices approval, market development, and effective product maintenance. Specialist, Pharmacovigilance Your Job Management of safety- related information from all sources (incl. but not limited to spontaneous, literature, clinical studies, medical information enquiries) Case intake (data entry) , translation into English, quality check (without case assessment) , documentation of the case in the applicable tracker (s) Screening of local scientific literature (safety relevant publications) and identification of potential safety- relevant information. Support with creation of Individual Case Safety Reports (ICSR) of adverse events deriving from clinical trials, spontaneous reporting systems and from the literature Reporting of ICSRs to local competent authorities, based on the national PV reporting [...]
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Job vom 20.11.2024 Regulatory/ Clinical Affairs (RA/ CA) Team Lead (m/f/x) • Jena, Thüringen Führungs-/ Leitungspositionen

MEHR

[...] to function optimally. Medical technology from ZEISS supports medical professionals in improving the lives of patients worldwide. The fact that our actions have a direct impact on peoples well- being is what drives us every day. Your Role You are specialist and disciplinary manager of the Regulatory and Clinical Affairs department of one or more product lines in the respective division (BS) . You are overseeing a team with [...] the product line, implementing the Regulatory Affairs Lifecycle or Clinical Affairs (Clinical Evaluation and Strategy) . You are supporting the further development of the department, effectively enhancing expertise by introducing innovative concepts for the design and implementation of (global) clinical trials. You are fostering collaboration with interface departments and guarantee increased value to our specialty department. Your Profile Completed natural science [...]

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