38 Jobs für Clinical Trial Specialist
Stellenangebote Clinical Trial Specialist Jobs
Job vor 13 Tagen bei Jobleads gefunden
• Hamburg
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full service-capabilities, [...]
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[...] resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. Key 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 [. .. ] 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-[. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Freelance Senior/ Medical Director (Neurology-Bid Defense Support)
• München, Bayern
Führungs-/ Leitungspositionen Freiberuflich
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full service-capabilities, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Senior/ Medical Director (Neurology-Bid Defense Support) . About this role TFS Health Science is seeking a highly flexible board-certified Neurology specialist to support upcoming Bid Defense Meetings. This freelance role involves contributing expert input during proposal preparation (e. g. protocol review) and participating in the Bid Defense Meeting itself. Ideally, the successful candidate would also be available for medical monitoring support if the project is awarded although this is not a [. .. ] a key scientific advisor in bid defense meetings (BDM) , RFP responses, and proposal development, ensuring compelling and medically sound strategies. Study Design Protocol Development : Provide expert input on trial design, patient recruitment, and regulatory strategy to optimize study success. Medical Oversight : Lead medical monitoring activities across assigned projects and step in as a handson medical monitor when needed. Scientific Advocacy : Represent TFS at client meetings, industry conferences, and scientific events, reinforcing our reputation as a trusted CRO [. .. ]
Job am 04.12.2025 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• München, Bayern
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full service-capabilities, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] resourcing and Functional Service (FSP) solutions. About this role As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. Key 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 [. .. ] 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-[. .. ]
Job am 27.06.2025 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
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 [. .. ]
Job gestern bei Jobleads gefunden
• München, Bayern
Clinical Operations
Specialist Contracts (m/f/d) Site Name: Munich Prinzregentenplatz Posted Date: Dec 17 2025 Bei GSK haben wir ehrgeizige Ziele für Patienten und setzen uns dafür ein, die Gesundheit von [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 2, 5 Milliarden Menschen bis zum Ende des Jahrzehnts positiv zu beeinflussen. R D setzt sich dafür ein, innovative Impfstoffe und [. .. ] Konsistenz, Kostenoptimierung und Risikominimierung sicherzustellen. Budgetaktualisierungen in Verträgen aufgrund von Protokolländerungen und Beratung bei der Anpassung des Studienbudgets sowie Identifikation von Kostenabweichungen und Möglichkeiten zur Kostenvermeidung. Sicherstellung der Vollständigkeit der Trial Master File (TMF) für alle Budget- und Vertragsaktivitäten und Unterstützung bei weiteren Aufgaben im Studienverlauf gemäß absolviertem Training. Qualifikationen Fähigkeiten Bachelor-Abschluss oder gleichwertiger Abschluss in einem wissenschaftlichen Bereich wie Biowissenschaften, Medizin, klinische Forschung, Pharmazie oder einem verwandten Fachgebiet. Relevante Erfahrung in der klinischen Forschung Fundierte Kenntnisse im Erstellen und [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Clinical Operations Specialist Contracts (m/f/d)
• München, Bayern
[. .. ] Krankheitsmechanismen zu entwickeln und die medizinische Entdeckung zu transformieren. Wir revolutionieren unsere R D. Wir vereinen Wissenschaft, Technologie und Talente, um gemeinsam der Krankheit einen Schritt voraus [...]
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[...] zu sein. Als Clinical Operations Specialist führen und koordinieren Sie Aktivitäten im Zusammenhang mit Einreichungen gemäß ICH GCP, internationalen und lokalen Vorschriften sowie relevanten GSK-Standards. In dieser zentralen Rolle innerhalb unseres lokalen klinischen Studienteams sind Sie maßgeblich an der Planung, Durchführung und Überwachung klinischer Studien im Land beteiligt. Hauptaufgaben Koordination und Verwaltung von Verträgen und [. .. ] Konsistenz, Kostenoptimierung und Risikominimierung sicherzustellen. Budgetaktualisierungen in Verträgen aufgrund von Protokolländerungen und Beratung bei der Anpassung des Studienbudgets sowie Identifikation von Kostenabweichungen und Möglichkeiten zur Kostenvermeidung. Sicherstellung der Vollständigkeit der Trial Master File (TMF) für alle Budget- und Vertragsaktivitäten und Unterstützung bei weiteren Aufgaben im Studienverlauf gemäß absolviertem Training. Qualifikationen Fähigkeiten Bachelor-Abschluss oder gleichwertiger Abschluss in einem wissenschaftlichen Bereich wie Biowissenschaften, Medizin, klinische Forschung, Pharmazie oder einem verwandten Fachgebiet. Relevante Erfahrung in der klinischen Forschung. Fundierte Kenntnisse im Erstellen und [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Accompanying applications (
trial order of measurement parameters and products) in the field of non-invasive patient monitoring at the customers site Development and implementation of individual overall solutions for the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] customer together with the sales staff and subsequent continued support Training of clinical and nursing staff in the companys own training center or in hospitals Product presentation in workshops, at trade fairs and congresses Documentation and forwarding of customer feedback in the CRM system Collaboration with national and international teams such as Customer Service, Marketing and Technical Service Traveling in the assigned region [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Senior Software Engineer KI (all genders)
• Bonn, Nordrhein- Westfalen
Homeoffice möglich
[. .. ] function Other Industries IT Services and IT Consulting Referrals increase your chances of interviewing at adesso SE by 2x Sign in to set job alerts for Summer [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Staff roles. Freelance Clinical Trial Site Coordinator Cologne, North Rhine-Westphalia, Germany 1 week ago Trainee-Programm Financial Consultant (BWL, Finanzen, VWL) (w/m/d) Cologne, North Rhine-Westphalia, Germany 5 days ago Pedagogical specialist-elementary school child care Cologne, North Rhine-Westphalia, Germany 1 day ago Working Student Finance Procurement (m/f/x) Cologne, North Rhine-Westphalia, Germany 1 day ago Cologne, North Rhine-Westphalia, Germany 3 days ago Cologne, North Rhine-Westphalia, Germany 5 days ago Cabin Crew Online Information Day Cologne 4 [. .. ]
Job am 09.12.2025 bei Jobleads gefunden
[. .. ] to marketbased overpayment depending on professional qualification and experience. Responsibilities In this role you will carry out the responsibilities within the framework of contribution to multidisciplinary teams [...]
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[...] including outcomes research, clinical research, regulatory affairs and marketing staff to support product development, launch, marketing, patient access acceleration, reimbursement and formulary acceptance. Deliver relevant data and tools to meet country Health Technology Assessment (HTA) / reimbursement/ funding and access needs within the region. Identify and pursue opportunities to obtain reimbursement and provide support [. .. ] including costeffectiveness, budget impact, and costofillness analyses to support market access strategies. Develop product value stories and identify the evidence needs specific for reimbursement and influence the regional/ global clinical trial program to fill clinical data gaps. Analyse and communicate the relevant evidence effectively to target audiences within the region, including publication of research findings. Develop and deliver focused regional master files/ value dossier for effective and timely use in countries. Support local countries with selected reimbursement/ funding/ HTA submissions. In [. .. ] Economics or Life Science. Min 5 years experience in Reimbursement, Health economics, HTA and funding applications in a healthcare environment at a medical device or pharmaceutical or biotechnology or a specialist R HE in consulting company. Track record of developing and delivering reimbursement/ market access strategy in Germany is a must. Experience with strategic value story development and in conducting outcomes research project. Good understanding of the application, development and value assessment of health economic modelling. Excellent oral and written communication [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
Field Clinical Therapy Specialist
• Düsseldorf, Nordrhein- Westfalen
[. .. ] to the latest tools, information and training, well help you in advancing your skills and career. Here, youll be supported in progressing whatever your ambitions. About the [...]
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[...] role The Field Clinical Therapy Specialist will serve as the primary therapy expert for the Interventional Spine team across the EMEA region. This position is part of the Interventional Spine (IVS) team, supporting the Intracept procedureand will have responsibility for educating and training physicians and health care professional staff on Intracepts therapies to support clinical studies [. .. ] support the launch of new products and sales tools with comprehensive training materials. Assist the execution and delivery of procedural training to physicians and medical staff in support of clinical trial site initiation and qualification for ongoing and future clinical studies. Attend case coverage and technical support for clinical sites requiring supplemental training or education. Interact in the field and evaluate need for new learning programs, educational materials and handson equipment/ models to address unmet education needs for customers and employees; [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
[. .. ] to the latest tools, information and training, well help you in advancing your skills and career. Here, youll be supported in progressing whatever your ambitions. About the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] role: The Field Clinical Therapy Specialist will serve as the primary therapy expert for the Interventional Spine team across the EMEA region. This position is part of the Interventional Spine (IVS) team, supporting the Intracept procedureand will have responsibility for educating and training physicians and health care professional staff on Intracepts therapies to support clinical studies [. .. ] support the launch of new products and sales tools with comprehensive training materials. Assist the execution and delivery of procedural training to physicians and medical staff in support of clinical trial site initiation and qualification for ongoing and future clinical studies. Attend case coverage and technical support for clinical sites requiring supplemental training or education. Interact in the field and evaluate need for new learning programs, educational materials and handson equipment/ models to address unmet education needs for customers and employees; [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
Clinical Operations Specialist
• München, Bayern
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to address modern [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only makeneos Health easier to work [. .. ] as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure compliance with protocol requirements, study procedures and relevant guidelines Creates and assists with maintenance of Trial Master File (TMF) and project files, including participation in file audits Prepares and maintains site manuals, reference tools and other documents Maintains, updates, and inputs clinical tracking information into databases Tracks incoming and outgoing clinical and regulatory documents and updates for investigator sites, studies, project team, or client Manages shared [. .. ]
Job am 05.12.2025 bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
[. .. ] often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a patients unmet clinical needs. Its our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. Since 2017, Edwards TMTT launched more than 4 products transformational therapies in Europe led by its PASCAL and EVOQUE programs. Every patient is different-be an expert on our PASCAL device/ therapy and helppatients suffering from mitral and tricuspid diseases The Field Clinical Specialist is responsible for educating physicians on Pascal technologies, device handling, implantation and troubleshooting techniques and case support by assigned hospitals/in assigned territories/ regions. Territory Germany (Düsseldorf, Köln, Bonn, Aachen) travelling required If you are considering relocating to the region, we are open to it and happy to support you [. .. ] on one technology. Responsible for upselling in key strategic accounts working in conjunction with Business Managers 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 am 05.12.2025 bei Jobleads gefunden
Scientist for Bioinformatic Analysis (f/m/x)
Homeoffice möglich
[. .. ] scientific knowledge and the improvement of peoples quality of life. Provide bioinformatics and statistical support to researchers and clinicians across the institute Conduct statistical analyses, data interpretation, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and visualization of clinical trial datasets Perform comprehensive bioinformatics and statistical analyses of high-dimensional omics datasets (spatial, single-cell, and bulk) Integrate and analyze multiple omics layers (e. g. , genomics, transcriptomics, proteomics, epigenomics) to uncover biological mechanisms and identify clinical biomarkers Develop, maintain, and document analysis pipelines and software tools to ensure reproducible [. .. ] leave, flexi days, plus public holidays International Staff Service: Support with the relocation and integration process in Germany Our recruiting is decentralized your application will be reviewed directly by the specialist department in which you could work in the future. More information about our application process Please send your application only via our online application tool and with the following documents: CV Degrees/ Diplomas/ Certificates Contact details for at least two referees If you have obtained a university degree abroad, we [. .. ]
Job am 02.12.2025 bei Jobleads gefunden
• Leipzig, Sachsen
Homeoffice möglich
[. .. ] scientific knowledge and the improvement of peoples quality of life. Provide bioinformatics and statistical support to researchers and clinicians across the institute Conduct statistical analyses, data interpretation, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and visualization of clinical trial datasets Perform comprehensive bioinformatics and statistical analyses of high-dimensional omics datasets (spatial, single-cell, and bulk) Integrate and analyze multiple omics layers (e. g. , genomics, transcriptomics, proteomics, epigenomics) to uncover biological mechanisms and identify clinical biomarkers Develop, maintain, and document analysis pipelines and software tools to ensure reproducible [. .. ] leave, flexi days, plus public holidays International Staff Service: Support with the relocation and integration process in Germany Our recruiting is decentralized-your application will be reviewed directly by the specialist department in which you could work in the future. More information about our application process Please send your application only via our online application tool and with the following documents: CV Degrees/ Diplomas/ Certificates Contact details for at least two referees If you have obtained a university degree abroad, we [. .. ]
Job am 02.12.2025 bei Jobleads gefunden
Scientist for Bioinformatic Analysis (f/m/x)
• Leipzig, Sachsen
Homeoffice möglich
[. .. ] scientific knowledge and the improvement of peoples quality of life. Provide bioinformatics and statistical support to researchers and clinicians across the institute Conduct statistical analyses, data interpretation, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and visualization of clinical trial datasets Perform comprehensive bioinformatics and statistical analyses of high-dimensional omics datasets (spatial, single-cell, and bulk) Integrate and analyze multiple omics layers (e. g. , genomics, transcriptomics, proteomics, epigenomics) to uncover biological mechanisms and identify clinical biomarkers Develop, maintain, and document analysis pipelines and software tools to ensure reproducible [. .. ] leave, flexi days, plus public holidays International Staff Service: Support with the relocation and integration process in Germany Our recruiting is decentralized-your application will be reviewed directly by the specialist department in which you could work in the future. More information about our application process Please send your application only via our online application tool and with the following documents: CV Degrees/ Diplomas/ Certificates Contact details for at least two referees If you have obtained a university degree abroad, we [. .. ]
Job am 01.12.2025 bei Jobleads gefunden
A leading biopharmaceutical solutions organization in Switzerland seeks a Global
Trial Optimization
Specialist to support
clinical study planning and recruitment. Responsibilities include creating recruitment materials, managing recruitment [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] vendors, and contributing to process improvements. The position offers comprehensive benefits including health insurance, a possible company car, and flexible paid time off. #J-18808-Ljbffr 70991054 [. .. ]
Job am 24.11.2025 bei Jobleads gefunden
Senior Reimbursement Analyst (m/f/d) - EMEA
• Schweinheim, Nordrhein- Westfalen
[. .. ] include the following and other duties may be assigned : In this role you will carry out the responsibilities within the framework of contribution to multidisciplinary teams [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] including outcomes research, clinical research, regulatory affairs and marketing staff to support product development, launch, marketing, patient access acceleration, reimbursement and formulary acceptance. Deliver relevant data and tools to meet country Health Technology Assessment (HTA) / reimbursement/ funding and access needs within the region. Identify and pursue opportunities to obtain reimbursement and provide support [. .. ] including costeffectiveness, budget impact, and costofillness analyses to support market access strategies. Develop product value stories and identify the evidence needs specific for reimbursement and influence the regional/ global clinical trial program to fill clinical data gaps. Analyse and communicate the relevant evidence effectively to target audiences within the region, including publication of research findings. Develop and deliver focused regional master files/ value dossier for effective and timely use in countries. Support local countries with selected reimbursement/ funding/ HTA submissions. In [. .. ] Economics or Life Science. Min 5 years experience in Reimbursement, Health economics, HTA and funding applications in a healthcare environment at a medical device or pharmaceutical or biotechnology or a specialist R HE in consulting company. Track record of developing and delivering reimbursement/ market access strategy in Germany is a must. Experience with strategic value story development and in conducting outcomes research project. Good understanding of the application, development and value assessment of health economic modelling. Excellent oral and written communication [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Senior Reimbursement Analyst (m/f/d) - EMEA
• Meerbusch, Nordrhein- Westfalen
[. .. ] effectiveness, budget impact, and cost-of-illness analyses to support market access strategies. Develop product value stories and identify the evidence needs specific for reimbursement and influence the regional/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] global clinical trial program to fill clinical data gaps. Analyse and communicate the relevant evidence effectively to target audiences within the region, including publication of research findings. Develop and deliver focused regional master files/ value dossiers for effective and timely use in countries. Support local countries with selected reimbursement/ funding/ HTA submissions. In [. .. ] Economics or Life Science. Min 5 years experience in Reimbursement, Health economics, HTA and funding applications in a healthcare environment at a medical device or pharmaceutical or biotechnology or a specialist R HE in consulting company. Track record of developing and delivering reimbursement/ market access strategy in Germany is a must. Experience with strategic value story development and in conducting outcomes research project. Good understanding of the application, development and value assessment of health economic modelling. Excellent oral and written communication [. .. ]
Job am 17.11.2025 bei Jobleads gefunden
Clinical Operations Specialist-Munich area
• München, Bayern
Clinical Operations
Specialist-Munich area Updated: Yesterday Location: DEU-Remote Job ID: 25103690 Clinical Operations Specialist-Munich area Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model [. .. ] Clinical Operations Policies, SOPs, and Work Instructions. Assist Clinical Monitoring staff with site management activities, serving as a Sponsor representative for assigned studies and ensuring protocol compliance. Create and maintain Trial Master File (TMF) and project files, including participation in file audits. Prepare and maintain site manuals, reference tools, and other documents. Maintain and input clinical tracking information into databases. Track clinical and regulatory documents and update for investigator sites, studies, and project team. Manage shared mailbox, process site requests and [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Executive Medical Director Clinical Development Endocrinology, Europe
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] for tardive dyskinesia, chorea associated with Huntingtons disease, classic congenital adrenal hyperplasia, endometriosis and uterine fibroids, as well as a robust pipeline including multiple compounds in mid-to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, [. .. ] Monitoring patient safety and the overall benefit-risk profile of investigational drugs throughout the clinical trials in collaboration with Drug Safety and Pharmacovigilance Leads analysis, interpretation, and presentation of clinical trial data to internal and external audiences e. g. decision making, regulatory submissions, and scientific disclosures including conference abstracts and publication of manuscripts Engage with and foster strong relationships with key opinion leaders and investigators to incorporate clinical insights into internal strategy and ensure optimal clinical trial execution Collaborate closely with [. .. ] of data and identification of evidence generation needs Adhere to Neurocrine Europe quality assurance system and compliance with the relevant SOPs Requirements: The appointed candidate will be a physician with specialist experience/ qualifications in endocrinology and/or a proven track record of clinical development in endocrinology products. MD qualified, ideally with specialist medical qualification in Endocrinology and previous experience in patient care At least 8 years experience in early or late stage clinical development in the pharmaceutical industry, ideally including experience [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
Senior Reimbursement Analyst (m/f/d) - EMEA
• Wien
[. .. ] may include the following and other duties may be assigned:In this role you will carry out the responsibilities within the framework of contribution to multi-disciplinary teams including [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outcomes research, clinical research, regulatory affairs and marketing staff to support product development, launch, marketing, patient access acceleration, reimbursement and formulary acceptance. Deliver relevant data and tools to meet country Health Technology Assessment (HTA) / reimbursement/ funding and access needs within the region. Identify and pursue opportunities to obtain reimbursement and provide support [. .. ] budget impact, and cost-of-illness analyses to support market access strategies. Develop product value stories and identify the evidence needs specific for reimbursement and influence the regional/ global clinical trial program to fill clinical data gaps. Analyse and communicate the relevant evidence effectively to target audiences within the region, including publication of research findings. Develop and deliver focused regional master files/ value dossier for effective and timely use in countries. Support local countries with selected reimbursement/ funding/ HTA submissions. In [. .. ] Economics or Life Science. Min 5 years experience in Reimbursement, Health economics, HTA and funding applications in a healthcare environment at a medical device or pharmaceutical or biotechnology or a specialist R HE in consulting company. Track record of developing and delivering reimbursement/ market access strategy in Germany is a must. Experience with strategic value story development and in conducting outcomes research project. Good understanding of the application, development and value assessment of health economic modelling. Excellent oral and written communication [. .. ]
Job am 04.11.2025 bei Jobleads gefunden
Quality Regulatory Dossier Compliance Specialist (m/f/d)
• München, Bayern
[. .. ] Freiburg) . The Courroux site is multifunctional, specialized in manufacturing parenteral products, it employs over 100 employees, and is recognized as a European leader in the manufacture [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and supply of clinical trial medications. Adragos Jura is seeking a Regulatory Dossier Compliance Specialist to support regulatory compliance and contribute to the submission and maintenance of national and international authorizations for our customers. The role will operate under the guidance of a Quality Compliance Systems Team Leader and will involve collaboration with crossfunctional teams both internally and with customers to ensure timely and accurate [. .. ]
Job am 31.10.2025 bei Jobleads gefunden
Contract Specialist-Germany-hybrid in München
• München, Bayern
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to address modern [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work, to make Syneos Health easier to work with [. .. ] to: Life Cycle maintenance regulatory activities (study maintenance and amendment submissions, oversight of communication to competent authorities/ ethics committees, import/ export license extensions) Oversight of delivery of executed amended clinical trial agreements and investigator budgets with investigator sites Overall SSU timelines following site activation. Including any realignment required due to amendment needs. Updates plans in accordance with Standard Operating Procedures and/or sponsorscoped processes. Complies all controlled document requirements and other requirements to ensure quality deliverables. Develops and manages integrated timelines [. .. ]
Job am 10.10.2025 bei Jobleads gefunden
Project Manager-Remote
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial insights into outcomes to address modern [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] together diversity of thoughts, backgrounds, cultures, and perspectives were able to create a place where everyone feels like they belong. Job Responsibilities Under the mentorship of the Indication Lead Global Trial Optimization Specialist, will create functional area deliverables that support clinical study planning and recruitment. These may include but are not limited to: Creation of patient and site facing recruitment materials Creation of the site feasibility questionnaire Creation of trial and program level slide decks Project management of recruitment vendors Database searches and [. .. ]
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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 38 offene Stellenanzeigen für Clinical Trial Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Specialist Jobs?
Aktuell suchen 10 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:
- Edwards Lifesciences (5 Jobs)
- GSK (1 Job)
- ICON (1 Job)
- Sound United (1 Job)
- Proclinical (1 Job)
- Boston Scientific (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Specialist Jobs werden derzeit in Bayern (9 Jobs), Nordrhein-Westfalen (7 Jobs) und Niedersachsen (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Specialist Jobs?
Clinical Trial Specialist Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
