483 Jobs für Clinical Trials Management
Stellenangebote Clinical Trials Management Jobs
Job vor 3 Tagen bei StepStone gefunden
ZEISS
• Aalen (Baden- Württemberg)
Beratungs-/ Consultingtätigkeiten
[. .. ] Oversee preparation and submission of regulatory documents to authorities Ensure compliance of all products throughout their lifecycle, from authorization to discontinuation and ensure regulatory compliance for product [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] labeling and support clinical trials Lead efforts to obtain necessary approvals and licenses in various markets (e. g. , EU MDR, UK MDR) Integrate regulatory elements into business processes to minimize approval delays and rejections Maintain and update regulatory documentation related to Quality Management Systems and assess marketing claims BS/ MSc in Life Sciences, Engineering, Optics, Regulatory Affairs and/or related experience Strong experience in regulatory affairs and quality management, preferably in medical devices, ideally with experience in standalone or embedded medical device software and IEC 62304, or in pharma Understanding and proven track [. .. ]
Job vor 4 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
Lead Medical Writer (m f d)
• 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 vor 4 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
• 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 4 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 4 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 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 9 Tagen bei Stellen-Online gefunden
Link Medical
• 10783, Berlin 10783, 10783 Berlin, Berlin
Führungs-/ Leitungspositionen
[. .. ] we currently have an open position at our office in Berlin (DE) LINK Medical is searching for a highly motivated Local Regulatory Contact Study Start-Up (SSU) / [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regulatory Lead (Clinical Studies) / (Sr) CRA in Germany. As a Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) , you will work in close collaboration with members of internal and external project teams, with local and international projects, and within a range of different therapeutic areas. This role can also be combined [. .. ] study submissions. Provide guidance (internal and external) on regulatory requirements. Optional (dependent on previous experience) : Contribute to and coordinate regulatory and EC clinical study application submissions for multi country trials (including submissions for Clinical Trials with IMPs via CTIS) . If applicable also work partly as CRA including:Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ ISO 14155, SOPs, and regulations. Serve as main point of contact with the study site. Perform Source Data Review [. .. ] and national regulations. Experience in clinical trials submissions for both investigational medicinal products and medical device locally and preferably also internationally incl. UK Experience in monitoring clinical studies and site management is preferable, but not a requirement. Fluent in the local language and English. Strong writing and IT skills. We offer LINK Medical offers an exciting and challenging position in a European CRO that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of our [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Link Medical
Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) / (Sr) CRA at LINK Medical (DE)
• berlin
Führungs-/ Leitungspositionen
[. .. ] we currently have an open position at our office in Berlin (DE) LINK Medical is searching for a highly motivated Local Regulatory Contact Study Start-Up (SSU) / [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regulatory Lead (Clinical Studies) / (Sr) CRA in Germany. As a Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) , you will work in close collaboration with members of internal and external project teams, with local and international projects, and within a range of different therapeutic areas. This role can also be combined [. .. ] study submissions. Provide guidance (internal and external) on regulatory requirements. Optional (dependent on previous experience) : Contribute to and coordinate regulatory and EC clinical study application submissions for multi country trials (including submissions for Clinical Trials with IMPs via CTIS) . If applicable also work partly as CRA including: Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ ISO 14155, SOPs, and regulations. Serve as main point of contact with the study site. Perform Source Data [. .. ] and national regulations. Experience in clinical trials submissions for both investigational medicinal products and medical device locally and preferably also internationally incl. UK Experience in monitoring clinical studies and site management is preferable, but not a requirement. Fluent in the local language and English. Strong writing and IT skills. We offer LINK Medical offers an exciting and challenging position in a European CRO that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of [. .. ]
Job vor 5 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 9 Tagen bei JobMESH gefunden
Link Medical
Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) / (Sr) CRA at LINK Medical (DE)
• State of Berlin 10783
Führungs-/ Leitungspositionen
[. .. ] we currently have an open position at our office in Berlin (DE) LINK Medical is searching for a highly motivated Local Regulatory Contact Study Start-Up (SSU) / [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regulatory Lead (Clinical Studies) / (Sr) CRA in Germany. As a Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) , you will work in close collaboration with members of internal and external project teams, with local and international projects, and within a range of different therapeutic areas. This role can also be combined [. .. ] study submissions Provide guidance (internal and external) on regulatory requirements Optional (dependent on previous experience) : Contribute to and coordinate regulatory and EC clinical study application submissions for multi country trials (including submissions for Clinical Trials with IMPs via CTIS) If applicable also work partly as CRA including Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ ISO 14155, SOPs, and regulations. Serve as main point of contact with the study site Perform Source Data Review [. .. ] and national regulations Experience in clinical trials submissions for both investigational medicinal products and medical device locally and preferably also internationally incl. UK Experience in monitoring clinical studies and site management is preferable, but not a requirement Fluent in the local language and English Strong writing and IT skills We offer LINK Medical offers an exciting and challenging position in a European CRO that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of [. .. ]
Job gestern 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 vor 9 Tagen bei Jooble gefunden
Link Medical
Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) / (Sr) CRA at LINK Medical (DE)
• Schleswig
Führungs-/ Leitungspositionen
[. .. ] we currently have an open position at our office in Berlin (DE) LINK Medical is searching for a highly motivated Local Regulatory Contact Study Start-Up (SSU) / [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regulatory Lead (Clinical Studies) / (Sr) CRA in Germany. As a Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) , you will work in close collaboration with members of internal and external project teams, with local and international projects, and within a range of different therapeutic areas. This role can also be combined [. .. ] This includes both medicinal products and medical device studies and interventional as well as non-interventional studies. ) If applicable also work partly as CRA including: Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ ISO 14155, SOPs, and regulations. Perform Source Data Review (SDR) , Source Data Verification (SDV) and review Case Report Forms (CRFs) . Bachelors degree or equivalent in a relevant field. Experience in clinical trials submissions for both investigational medicinal products and [. .. ] Besides a great working environment with dedicated and supporting colleagues, we also offer a competitive compensation, benefit scheme and great development opportunities for all employees. Elin Nilsson, Director Clinical Project Management, xiummaj Please submit your application in English. 72564460 [. .. ]
Job vor 10 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 [. .. ]
Job gestern bei Jobleads gefunden
Regional Medical Science Liaison Chronic Cough (mfd)
• 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 gestern bei Jobleads gefunden
• 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 3 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 3 Tagen bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] Dermatologist-Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. Hybrid WFH Flexibility All Medical Directors have hybrid WFH flexibility. Responsibilities Provide medical management and expertise for clinical trials; Contribute medical expertise to study reports, regulatory documents, and manuscripts; Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; Participate in new business development through involvement in proposal and sponsor meetings as requested; Coordinate with other [. .. ]
Job vor 6 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 12 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 [...]
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 : [. .. ]
Job am 08.12.2025 bei Jobleads gefunden
Global Head of Pharmacovigilance
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] compliance, and driving successful trial conduct for company assets across all stages of development. This be responsible for directing safety strategy, operations, and regulatory compliance for oncology [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] drug products across clinical development and commercialisation phases. This leadership role is central to ensuring safe, compliant, and successful oncology drug development and to maximising patient safety from clinical trials to post-marketing surveillance. This position will report to the Chief Medical Officer and either work on a hybrid basis from the company office in Germany or on a remote basis. Your mission Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory [. .. ] regulatory specialists, fostering a collaborative and high-performance culture. Medical oversight of safety data, including the review of case safety reports (SAEs, SUSARs) and aggregate analyses. Establish and maintain risk management plans, safety monitoring plans, data exchange agreements, and readiness for health authority inspections. Represent the company in safety-related interactions with regulatory agencies, partners, and external stakeholders. Collaborate cross-functionally with clinical development, regulatory, medical affairs, and other teams integrating safety across the product lifecycle. Ideally, you will have : [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
SVP Head of Cardio-Renal Research (all genders)
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] therapeutic area, including internal projects and strategic collaborations Prioritize and oversee earlystage R D initiatives, from target identification to preclinical development Provide scientific leadership and collaborate with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Operations, Key Account Management and Business Development to identify, shape, and convert R D projects into partnerships Represent Evotecs expertise at customer events, scientific conferences, consortia, and in peerreviewed 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 [. .. ] value chain and project deliverables with in-depth subject matter expertise for cardiorenal 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 discoverystage programs and strategic collaborations Experience in licensing, partnering, and external scientific representation Strong network and credibility in the cardiorenal field Skills Competencies Strategic and systems thinker with a futureoriented mindset Strong leadership and influencing skills in a matrix environment [. .. ]
Job am 06.12.2025 bei Jobleads gefunden
Executive CSO-Oncology Trials Strategic Leadership
• Bern
Führungs-/ Leitungspositionen
A leading Swiss oncology research institute is seeking a Chief Scientific Officer (CSO) to lead the
Clinical Science team. This role involves developing and implementing clinical
trials, building [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] partnerships with the industry, and overseeing research innovations within Switzerland. The ideal candidate will have a medical or scientific background (Md/Ph D) , proven leadership experience, and fluency in English plus German and/or French. This is a unique opportunity to contribute significantly to the advancement of oncology research. [. .. ]
Job am 06.12.2025 bei Jobleads gefunden
Chief Scientific Officer (CSO) Switzerland, 80 100 (Ref. 2605) - Member of the executive Board
• Bern
Führungs-/ Leitungspositionen
[. .. ] of the Executive Board role at Auriga Vision AG. Our client is the Swiss Cancer Institute (former SAKK) , a non-profit organization focused on the development and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] implementation of clinical trials in oncology based in Berne, Switzerland. As part of the teams expansion, we are looking for a Member of the executive Board. Responsibilities Leadership : Leading the Clinical Science team (Senior Scientific Director, Head of Clinical Development, Medical Science Liaison) , approximately 10 Clinical Scientists and Medical Advisors; active member of the Management Board for the Swiss organization, reporting to the CEO. Research Innovation : Translating projects into clinical trials; from study protocol to starting the clinical studies in Switzerland. Responsible for developing and implementing Investor Initiated Trials in Oncology in Switzerland Working closely with all leading oncology clinics across Switzerland. Scientific check [. .. ]
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 [...]
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 : [. .. ]
Job am 04.12.2025 bei Jobleads gefunden
Lead Medical Director CVRm/Heart Failure
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The Position Roches Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development clinical strategies and plans that deliver medically differentiated therapies that provide meaningful improvement to patients. Roche is looking for an experienced and highly specialized individual to join the Cardiovascular, Renal, and Metabolism group. [. .. ] guiding and shaping our cardiovascular outcomes strategy. To be successful in this role, you will need to have extensive experience in late stage drug development and managing large-scale clinical trials, including outcome studies, in particular we are looking for candidates with experience in heart failure programs. You will have strong collaboration with cross-functional teams, including clinical research, regulatory affairs, and medical affairs, to ensure the successful progression of treatments through the pipeline and into the market. The position would [. .. ] understanding of cardiovascular diseases, clinical trial protocols, regulatory requirements, and possibly interactions with regulatory agencies to ensure studies meet the required standards. The Opportunity You will interact with high level management and experts both internally and externally, serving as internal consultants. You are expected to provide critical insights and contributions to the development and effectiveness of the assigned project. You have demonstrated a high level of experience in Clinical Development Plan (CDP) Strategy Planning, Execution, Regulatory Activities, and Cross-Functional Team [. .. ]
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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 483 offene Stellenanzeigen für Clinical Trials Management Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Management Jobs?
Aktuell suchen 38 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 (32 Jobs)
- Tubulis GmbH (21 Jobs)
- TFS Health Science (15 Jobs)
- Astra Zeneca (12 Jobs)
- CCS- Global (11 Jobs)
- Veeda Lifesciences (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 (73 Jobs), Nordrhein-Westfalen (68 Jobs) und Berlin (46 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Management Jobs?
Clinical Trials Management Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
