460 Jobs für Clinical Trials Management
Stellenangebote Clinical Trials Management Jobs
Job vor 2 Tagen bei Jobleads gefunden
• Wien
[. .. ] entails providing leadership to the trial team, managing clinical trials planning, execution, and delivery while ensuring compliance with key performance indicators. The ideal candidate should have a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strong background in clinical trials management, effective communication skills, and experience in stakeholder engagement. This position offers the opportunity to work with diverse teams globally and contribute to advancing therapy delivery. #J-18808-Ljbffr 73332836 [. .. ]
Job vor 7 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
Senior Clinical Scientist Clinical Drug Development (m f d)
• Bergisch Gladbach
Homeoffice möglich
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 the market As a Senior Clinical Scientist in Clinical Drug Development, you will take on both strategic and operational responsibilities in advancing innovative therapies in autoimmune diseases, oncology, with a focus on advanced therapy medicinal products [. .. ] backwards from the desired final readouts to plan early for the necessary data, overseeing capture, coordinating cleaning and integrity checks, and obtaining study results in collaboration with biostatistics, programming, data management, and medical monitoring teamsensuring outputs that are decision-ready for regulatory and clinical use. You integrate translational insights, biomarkers, and clinical endpoints into development plans and work effectively across a matrix environment of internal stakeholders, external collaborators, and CRO partners to ensure alignment from early research through late-stage clinical [. .. ]
Job vor 7 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
• Bergisch Gladbach
Beratungs-/ Consultingtätigkeiten Homeoffice möglich
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 our pharmacological developments at all Job Description As a Process Design Expert within the Global Supply Chain (GSC) team of Miltenyi Biomedicine, you will play a key role in shaping [. .. ] hold a university degree in engineering, life sciences, economics, informatics, or a related field. You bring experience in process design, and documentation or manual writing as well as related project management-ideally within the pharmaceutical, logistics, or regulated environments. You have a strong analytical mindset and the ability to translate complex requirements into clear, actionable processes. You are a strong communicator who enjoys aligning with diverse stakeholders across functions and geographies and are comfortable with occasional business travel. Fluency in English [. .. ]
Job vor 7 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
Senior Project Manager-Drug Development (m f d)
• Bergisch Gladbach
Homeoffice möglich
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 the market. Job Description As Senior Project Manager, you will support global drug development programs from early development through to worldwide regulatory approval. In this role, you will lead the cross-functional project management effort, ensuring that timelines, interdependencies, and critical deliverables are aligned across all contributing functions. You will serve as the central operational driver to keep the project team coordinated, on track, and focused on achieving key development milestones. Key Responsibilites: Lead global project management activities for assigned drug-development programs, ensuring [. .. ]
Job vor 7 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
• Bergisch Gladbach
Führungs-/ Leitungspositionen Homeoffice möglich
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 the market. As a Medical Writer you are part of our Miltenyi biomedicine business and within the Clinical Development team. You will be responsible for the development and oversight of clinical and regulatory documents that support [. .. ] through mentoring and managing small teams, ensuring high-quality deliverables. Your profile is rounded by a solid understanding of drug development and regulatory frameworks (ICH, EMA, FDA) , excellent project management skills, and the ability to communicate complex scientific data clearly in English. Additional Information What we offer Working with free and self-determined time management, also mobile working An intercultural environment characterized by diversity and flat hierarchies Freedom to contribute creatively and play an active role in shaping the company [. .. ]
Job am 02.12.2025 bei StepStone gefunden
Danaher
Product Marketing Manager CC/ IA (f/m/d)
• Krefeld
Homeoffice möglich
[. .. ] and your unique viewpoint matter. And by harnessing Danahers system of continuous improvement, you help turn ideas into impact innovating at the speed of life. As a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratorys role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour [. .. ] with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible. The Product Marketing Manager CC/ IA is responsible for lifecycle management, marketing, and support of Clinical Chemistry and Immunoassays. Combines strategic marketing with hands-on operational tasks, including product launches, customer evaluations, training, and cross-functional collaboration. This position reports to the Marketing Manager DACH Region (Germany, Austria, Switzerland) and is located in Germany, remote. Join our winning team today. Together, [. .. ] that bring the power of science to life. For more information, visit In this role, you will have the opportunity to: Product Lifecycle: Forecasting, launches, obsolescence/ discontinuation, technical support, ring trials, QC updates, complaint handling. Customer Engagement: Manage evaluations (protocols, cost, evaluator follow-up) , present solutions at meetings/ events, maintain CCL communications. Cross-Product/ Expansion: Item creation, supplier onboarding, i Quote INLAB support, market expansion for 3rd party products. Training: Sales training (systems, assays) , onboarding of sales reps, EU Competitive [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Beckman Coulter- Diagnostics
• Krefeld, NW
[. .. ] and your unique viewpoint matter. And by harnessing Danahers system of continuous improvement, you help turn ideas into impact innovating at the speed of life. As a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratorys role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour [. .. ] with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible. The Product Marketing Manager CC/ IA is responsible for lifecycle management, marketing, and support of Clinical Chemistry and Immunoassays. Combines strategic marketing with hands-on operational tasks, including product launches, customer evaluations, training, and cross-functional collaboration. This position reports to the Marketing Manager DACH Region (Germany, Austria, Switzerland) and is located in Germany, remote. In this role, you will have the opportunity to: Product Lifecycle: Forecasting, launches, obsolescence/ discontinuation, technical support, ring trials, QC updates, complaint handling. Customer Engagement: Manage evaluations (protocols, cost, evaluator follow-up) , present solutions at meetings/ events, maintain CCL communications. Cross-Product/ Expansion: Item creation, supplier onboarding, i Quote INLAB support, market expansion for 3rd party products. Training: Sales training (systems, assays) , onboarding of sales reps, EU Competitive [. .. ]
Job vor 4 Tagen bei Neuvoo.com gefunden
Beckman Coulter- Diagnostics
Product Marketing Manager CC/ IA (f/m/d)
• North Rhine- Westphalia
[. .. ] and your unique viewpoint matter. And by harnessing Danahers system of continuous improvement, you help turn ideas into impact innovating at the speed of life. As a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratorys role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour [. .. ] with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible. The Product Marketing Manager CC/ IA is responsible for lifecycle management, marketing, and support of Clinical Chemistry and Immunoassays. Combines strategic marketing with hands-on operational tasks, including product launches, customer evaluations, training, and cross-functional collaboration. This position reports to the Marketing Manager DACH Region (Germany, Austria, Switzerland) and is located in Germany, remote. In this role, you will have the opportunity to: Product Lifecycle: Forecasting, launches, obsolescence/ discontinuation, technical support, ring trials, QC updates, complaint handling. Customer Engagement: Manage evaluations (protocols, cost, evaluator follow-up) , present solutions at meetings/ events, maintain CCL communications. Cross-Product/ Expansion: Item creation, supplier onboarding, i Quote INLAB support, market expansion for 3rd party products. Training: Sales training (systems, assays) , onboarding of sales reps, EU Competitive [. .. ]
Job gestern bei Mindmatch.ai gefunden
Novartis Pharmaceutical Manufacturing GmbH
• SZ schwaz
[. .. ] our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us Deliver technical development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and life-cycle management in cross-functional teams for easy-to-use, safe and robust products. Responsible for device constituent parts of an autoinjector, the system integration of prefilled syringes together with the autoinjector into a combination product and timely delivery of technical aspects of one or more projects as well as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience [. .. ]
Job gestern bei Mindmatch.ai gefunden
Novartis Pharmaceutical Manufacturing GmbH
Senior Expert Engineering Device Development (m/f/d)
• B bregenz
[. .. ] our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us Deliver technical development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and life-cycle management in cross-functional teams for easy-to-use, safe and robust products. Responsible for device constituent parts of an autoinjector, the system integration of prefilled syringes together with the autoinjector into a combination product and timely delivery of technical aspects of one or more projects as well as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience [. .. ]
Job gestern bei Mindmatch.ai gefunden
Novartis Pharmaceutical Manufacturing GmbH
Senior Expert Engineering Device Development (m/f/d)
• AT- 5 salzburg- umgebung
[. .. ] our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us Deliver technical development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and life-cycle management in cross-functional teams for easy-to-use, safe and robust products. Responsible for device constituent parts of an autoinjector, the system integration of prefilled syringes together with the autoinjector into a combination product and timely delivery of technical aspects of one or more projects as well as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience [. .. ]
Job gestern bei Mindmatch.ai gefunden
Novartis Pharmaceutical Manufacturing GmbH
Senior Expert Engineering Device Development (m/f/d)
• K villach
[. .. ] our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us Deliver technical development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and life-cycle management in cross-functional teams for easy-to-use, safe and robust products. Responsible for device constituent parts of an autoinjector, the system integration of prefilled syringes together with the autoinjector into a combination product and timely delivery of technical aspects of one or more projects as well as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience [. .. ]
Job gestern bei Mindmatch.ai gefunden
Novartis Pharmaceutical Manufacturing GmbH
Senior Expert Engineering Device Development (m/f/d)
• L linz- land
[. .. ] our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us Deliver technical development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and life-cycle management in cross-functional teams for easy-to-use, safe and robust products. Responsible for device constituent parts of an autoinjector, the system integration of prefilled syringes together with the autoinjector into a combination product and timely delivery of technical aspects of one or more projects as well as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience [. .. ]
Job gestern bei Mindmatch.ai gefunden
Novartis Pharmaceutical Manufacturing GmbH
Senior Expert Engineering Device Development (m/f/d)
• Y steyr
[. .. ] our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us Deliver technical development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and life-cycle management in cross-functional teams for easy-to-use, safe and robust products. Responsible for device constituent parts of an autoinjector, the system integration of prefilled syringes together with the autoinjector into a combination product and timely delivery of technical aspects of one or more projects as well as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience [. .. ]
Job gestern bei Mindmatch.ai gefunden
Novartis Pharmaceutical Manufacturing GmbH
Senior Expert Engineering Device Development (m/f/d)
• W wels
[. .. ] our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us Deliver technical development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and life-cycle management in cross-functional teams for easy-to-use, safe and robust products. Responsible for device constituent parts of an autoinjector, the system integration of prefilled syringes together with the autoinjector into a combination product and timely delivery of technical aspects of one or more projects as well as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience [. .. ]
Job gestern bei Mindmatch.ai gefunden
Novartis Pharmaceutical Manufacturing GmbH
Senior Expert Engineering Device Development (m/f/d)
• kirchdorf an der krems
[. .. ] our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us Deliver technical development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and life-cycle management in cross-functional teams for easy-to-use, safe and robust products. Responsible for device constituent parts of an autoinjector, the system integration of prefilled syringes together with the autoinjector into a combination product and timely delivery of technical aspects of one or more projects as well as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience [. .. ]
Job vor 13 Tagen bei Mindmatch.ai gefunden
team2work
• W wien
[. .. ] und auch laufend innovative, therapeutische Lösungen entwickeln und damit zur Verbesserung der Gesundheit und der Lebensqualität betroffener Menschen beitragen, suchen wir ab Jänner 2026 Regulatory Affairs Specialist [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] m/w/d Clinical Trials Applications (CTAs) : Unterstützung bei der Einreichung, Bewertung und Genehmigung von klinischen Studienanträgen gemäß EU-CT-Verordnung Funktion als Clinical Point of Contact im österreichischen RA-Team in enger Zusammenarbeit mit dem lokalen Clinical Trials Team Regulatorisches Umfeld: Aktuelle Kenntnis lokaler und internationaler Gesetze und Richtlinien Teilnahme an Konsultationen zu [. .. ] EMA für zugewiesene Produkte Verwaltung und Aufrechterhaltung bestehender Zulassungen durch fristgerechte Einreichung von Variations, Verlängerungsanträgen und ergänzenden Zulassungen Bearbeitung von Einwänden der Behörden und Verhandlung optimaler Zulassungsbedingungen Kennzeichnung und Artwork Management: Sicherstellung qualitativ hochwertiger Übersetzungen von Fachinformationen und Gebrauchsinformationen QRD-Prüfung und linguistische Kontrolle aller regulatorischen Dokumente Erstellung und Verwaltung von Verpackungsmaterialien gemäß Artwork Management System Implementierung von Verschreibungsinformationen innerhalb vorgegebener Fristen Stakeholder Management: Aufbau und Pflege positiver Beziehungen zu Zulassungsbehörden und der pharmazeutischen Industrie (Pharmig) Kommunikation regulatorischer Meilensteine an interne [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Director Project Management-Freelance
• München, Bayern
Führungs-/ Leitungspositionen Freiberuflich
About this role 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] expertise includes full-service capabilities, resourcing, and Functional Service Provider (FSP) solutions. The Director, Project Management is responsible for providing strategic and operational leadership across complex oncology projects. This role ensures end-to-end delivery excellence, timeline ownership, risk mitigation, and high-quality execution across multiple countries. As part of our SRS/ FSP team, you will be dedicated to one sponsor, a global pharmaceutical company with [. .. ] Sciences, Pharmacy, Medicine, or a related field; Masters degree preferred Extensive experience (10+ years) in clinical project management within a CRO or pharmaceutical environment Demonstrated leadership experience in Oncology clinical trials, with a strong focus on breast cancer studies Proven expertise in Real World Evidence (RWE) , Non-Interventional Studies Strong knowledge of ICH-GCP, EU regulatory requirements, and observational study regulations Excellent stakeholder management, communication, and leadership skills across cross-functional and cross-country teams What We Offer We provide [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• München, Bayern
Abgeschlossenes Studium Abgeschlossene Ausbildung
[. .. ] GSKs compliance to all federal and state US Transparency requirements. For more information please visit the Centers for Medicare and Medicaid Services (CMS) website at Key Skills [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Presentation Skills, Time Management, Clinical Research, Communication skills, GCP, Infusion Experience, Managed Care, Hospice Care, Conflict Management, Clinical Trials, Research Experience, Home Care Employment Type: Full-Time Experience: years Vacancy: 1 #J-18808-Ljbffr 73159343 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Associate Medical Director/ Medical Director
• Frankfurt (Oder) , Brandenburg
Führungs-/ Leitungspositionen
[. .. ] that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our Team As an Associate Medical Director/ Medical Director and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key member of the CTT. You will be part of a highly collaborative and cross-functional team involved with site evaluation, study start-up, study execution and management, and study close-out of our trials. This position will report to the VP, Clinical and Translational Development. The ideal candidate will be based in the Munich area, but remote locations in Germany are also acceptable. Your mission Provide clinical leadership and strategic medical input for all clinical deliverables in [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Manager Medical Science Liaison Oncology
• München, Bayern
[. .. ] aligned with local and European medical affairs priorities. Build and expand relationships/ networks with key medical and scientific experts in the field of breast cancer and/or lung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Inviations Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator-Initiated Trials, Real-World Evidence, and other evidence-generation studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing [. .. ] in GCP-compliant clinical trial support, with a solid understanding of trial design and execution. Exceptional ability to process, communicate, and present complex medical and scientific information effectively. Proven self-management and project management skills to independently plan and execute stakeholder engagement. Highest ethical standards with knowledge of clinical regulations, industry standards, and German codes of conduct. Fluent in German and English, with an entrepreneurial mindset, passion for innovation, and a can-do attitude. Benefits Your flexibility: flexible hours vacation account [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Medical Science Liaison Rare Tumour-Austria (all genders)
• Wien
[. .. ] regional, and national level. Serve as a scientific expert to the medical community and facilitate the appropriate exchange of scientific information. Communicate experts opinion and feedback on [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] new data and clinical trends to Medical Affairs and translate this information into strategic recommendations to enhance science and advance patient care. Act as primary liaison to investigators interested in developing and performing investigatorinitiated research. Collaborate with the Clinical Operations organization to enhance patient enrollment in companysponsored clinical trials by identifying appropriate clinical trial sites, supporting clinical trial awareness, and interacting with investigators in ongoing studies. Serve as medical lead and provide scientific support at medical congresses, support national and European medical booths staffing, participate and lead clinical support, and facilitate medical discussions at advisory boards and local scientific/ [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
SVP Head of Inflammation Immunology (all genders)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] area, including internal projects and strategic collaborations. Prioritize and oversee early-stage R D initiatives, from target identification to preclinical development. Provide scientific leadership and collaborate with Operations, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Key Account Management and Business Development to identify, shape, and convert Rn D projects into partnerships. Represent Evotecs expertise at customer events, scientific conferences, consortia, and in peer-reviewed publications. Knowledge Experience Ph D or equivalent in a relevant life science discipline Minimum 15 years of experience, with solid strategical and technical understanding of the [. .. ] project deliverables with in-depth subject matter expertise in the I I space Drug discovery experience from target ID to PDC of at least 10 years, exposure to planning of clinical development and trials up to Po Cs desirable Proven track record in progressing discovery-stage programs and strategic collaborations Experience in licensing, partnering, and external scientific representation Strong network and credibility in the I I field Skills Competencies Strategic and systems thinker with a future-oriented mindset Strong leadership and influencing skills in [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Senior Director, Pharmacometrics
• Berlin
Führungs-/ Leitungspositionen
[. .. ] and the people that need them most. Innovation and creativity are highly valued, and everyone is given the opportunity for training and continuous development. Our portfolio spans [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the discovery, preclinical, clinical and postmarketing phases of drug development, working with 1, 200 commercial companies, 250 academic institutions, and numerous regulatory agencies. In the past 6 years, over 90 of companies that received new drug approvals by the FDA used our software or services. Our integrated and proprietary endtoend platform with biosimulation, regulatory [. .. ] PD analyses, modelbased metaanalysis, doseresponse and exposureresponse analyses, dataset creation, disease modeling, trial simulation, optimal study designs, strategic decision analyses, economic modeling) . Experience in moving compounds through the clinical trials process and experience with various elements of clinical development and trial design and management and filings preferred. Certara bases all employmentrelated decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military [. .. ]
Job am 11.12.2025 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service-capabilities, 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, [. .. ] 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 Monitoring Signal Detection : Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions : Offer expert medical insight into regulatory submissions and 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 : [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Management pro Jahr?
Als Clinical Trials Management verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Management Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 460 offene Stellenanzeigen für Clinical Trials Management Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Management Jobs?
Aktuell suchen 37 Unternehmen nach Bewerbern für Clinical Trials Management Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Management Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Management Stellenangebote:
- Tigermed (22 Jobs)
- Tubulis GmbH (22 Jobs)
- TFS Health Science (15 Jobs)
- Astra Zeneca (12 Jobs)
- Veeda Lifesciences (11 Jobs)
- Bio Talent (11 Jobs)
In welchen Bundesländern werden die meisten Clinical Trials Management Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Management Jobs werden derzeit in Bayern (67 Jobs), Nordrhein-Westfalen (62 Jobs) und Berlin (44 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Management Jobs?
Clinical Trials Management Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
