16 Jobs für Clinical Trials Officer
Stellenangebote Clinical Trials Officer Jobs
Job vor 8 Tagen bei StepStone gefunden
Universitätsklinikum Carl Gustav Carus Dresden
• Dresden
Teilzeit
Jobticket Work-Life-Balance
[. .. ] and international research environment within the Else Kröner Fresenius Center for Digital Health at TU Dresden. While the institute has a strong focus on AI, this position [...]
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[...] has a broader clinical AI infrastructure mandate and will support projects across the center and its clinical partners that require access to routinely generated clinical data, prospective model evaluation, and robust research software and data infrastructure. The position is embedded into groups working at the intersection of AI development, clinical care, and translational research, [. .. ] is a hands-on data, software, and infrastructure role. Your work will help establish secure access to live or near-real-time clinical data, enable prospective shadow-mode evaluations (shadow trials) of AI models without influencing clinical decision-making, and build and maintain reusable research infrastructure. You will ensure that multimodal data along patients treatment pathways are reliably linked, securely stored and managed, and made available to researchers in a well-organized, privacy-compliant, and reproducible manner. Design, implement, and maintain [. .. ] practices Develop and maintain technical documentation, data dictionaries, provenance records, standard operating procedures, and reproducible onboarding materials for shared clinical AI infrastructure Liaise with the hospitals IT department, data protection officer, data integration center, clinical departments, and other infrastructure partners on data access, governance, prospective evaluation, and operational integration Support researchers across the group and collaborating clinical AI projects with data access, data quality questions, shadow-trial setup, and onboarding to shared infrastructure and workflows Profil University degree (Bachelors/ Masters level) [. .. ]
Job am 22.08.2026 bei Stellen-Online.de gefunden
Bio Marin Pharmaceutical
• Deutschland, 99986
Führungs-/ Leitungspositionen
[. .. ] span all areas of operations. Associate Director, Corporate Compliance Location: Frankfurt ( Hybrid role) Closing Date: 14 August 2026Summary Description The Associate Director, Corporate Compliance serves as [...]
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[...] the Country Compliance Officer for Germany and is the primary compliance business partner to the German leadership team. The role is responsible for overseeing the implementation and effectiveness of Bio Marin s Compliance Programme within Germany, providing strategic and practical advice on healthcare compliance matters, and fostering a culture of ethics and integrity throughout [. .. ] business policies and German law to ensure continuing relevance in providing guidance to management and employees; Collaborate with other company functions, including, but not limited to Commercial Operations, Medical Affairs, Clinical Sciences and Regulatory Affairs to provide advice and counsel regarding potential compliance issues and risks; Draft memoranda providing analysis and risk-based recommendations regarding various compliance rules and regulations implicated by proposed or existing business strategies; Evaluate, approve, and monitor company interactions with healthcare professionals, healthcare organisations, patient organisations and [. .. ] policies; Review of communications related to the companys development programmes to ensure they accurately and appropriately inform interested parties as to relevant information about the status and progress of clinical trials; Maintain an effective and proactive compliance communication and training programme in Germany (through Learning Management System and Live trainings) , including promoting use of the compliance hotline and expeditiously and thoroughly fielding questions relating to new and existing compliance issues and related policies and procedures raised by management and employees; [. .. ]
Job gestern bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] all areas of operations. Associate Director, Corporate Compliance Location: Frankfurt ( Hybrid role) Closing Date: 14 August 2026 Summary Description The Associate Director, Corporate Compliance serves as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Country Compliance Officer for Germany and is the primary compliance business partner to the German leadership team. The role is responsible for overseeing the implementation and effectiveness of Bio Marins Compliance Programme within Germany, providing strategic and practical advice on healthcare compliance matters, and fostering a culture of ethics and integrity throughout the [. .. ] business policies and German law to ensure continuing relevance in providing guidance to management and employees; Collaborate with other company functions, including, but not limited to Commercial Operations, Medical Affairs, Clinical Sciences and Regulatory Affairs to provide advice and counsel regarding potential compliance issues and risks; Draft memoranda providing analysis and risk-based recommendations regarding various compliance rules and regulations implicated by proposed or existing business strategies; Evaluate, approve, and monitor company interactions with healthcare professionals, healthcare organisations, patient organisations and [. .. ] policies; Review of communications related to the companys development programmes to ensure they accurately and appropriately inform interested parties as to relevant information about the status and progress of clinical trials; Maintain an effective and proactive compliance communication and training programme in Germany (through Learning Management System and Live trainings) , including promoting use of the compliance hotline and expeditiously and thoroughly fielding questions relating to new and existing compliance issues and related policies and procedures raised by management and employees; [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Allschwil, Basel- Landschaft
Contractor SVP
Clinical Development Fibrosis (Hepatology) Alentis Therapeutics AG-Allschwil The SVP of Clinical Development Fibrosis (Hepatology) , reporting to the Chief Medical
Officer, will oversee clinical research, medical management, and [...]
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[...] study execution for the Companys clinical program for Lixudebart and is a key member of the Research and Development Leadership Team. Tasks Provide medical and scientific leadership across the strategy, execution, interpretation, and communication of clinical data related to Lixudebart. Leading the strategic [. .. ] is required in addition to advanced knowledge and clinical training in medical/ scientific area; Hepatology practice experience 4 years. Experience with early and late stage clinical development research, including pivotal trials, in liver diseases, especially rare liver disease. Relationship and experience leading or being a critical team member for key regulatory activities, such as end-of-phase trial meetings, INDs, Marketing Authorization, special designations. Especially rare and liver divisions. Leading clinical program team in a matrix organization. Having high impact and [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Contractor SVP Clinical Development Fibrosis (Hepatology)
• Allschwil, Basel- Landschaft
Alentis Therapeutics, the Claudin-1 Company, is on a mission to treat cancer and reverse fibrosis. To this end, we are rapidly advancing a
clinical pipeline of anti-Claudin-1 monoclonal antibodies. Our [...]
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[...] team is committed to unlocking the broad potential of our therapeutic target Claudin-1 and bringing much-needed medicines to patients suffering from solid tumors as well as kidney, liver, and lung fibrosis. Tasks The SVP of Clinical Development Fibrosis (Hepatology) , reporting to the Chief Medical Officer, will oversee clinical research, medical management, and study execution for the Companys clinical program for Lixudebart and is a key member of the Research and Development Leadership Team. Leading the strategic development of Lixudebart in cooperation with the CMO and executive LT Provide medical and scientific leadership across the strategy, [. .. ] is required in addition to advanced knowledge and clinical training in medical/ scientific area; Hepatology practice experience 4 years. Experience with early and late stage clinical development research, including pivotal trials, in liver diseases, especially rare liver disease. Relationship and experience leading or being a critical team member for key regulatory activities, such as end-of-phase trial meetings, INDs, Marketing Authorization, special designations. Especially rare and liver divisions. Leading clinical program team in a matrix organization. Having high impact and [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Führungs-/ Leitungspositionen
Reporting directly to the Chief Medical
Officer (CMO) , the VP of Medical Affairs, is accountable for the management, development, and execution of the Medical Affairs departmentincluding the design [...]
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[...] and structure of the supporting functions of a Medical Affairs team such as Med Information, Medical Communications, Publications planning, Medical Science Liaisons, etc. , allocating and directing internal [. .. ] oncology, particularly cell therapy. Lead and manage field facing Medical Science Liaison team. Working with the CMO, in developing the strategy for Medical Affairs including external communications, publications, investigator sponsored Trials (ISTs) , congress and Advisory Boards planning and scientific communications. Lead publication planning and objectives and planning, CME education, symposia, and congress planning and assess full Medical Communication requirements to support launch. Assess and implement Medical Information requirements to support launch. Manage the investigator-initiated studies program review process post-[. .. ] ensure Medical Affairs activities are conducted according to Orcas policies and procedures, and in a manner compliant with all external laws and regulations. Collaborate closely with cross-functional teams, including Clinical Development, Clinical Operations, Project Management, Regulatory Affairs, and Commercial, to drive the successful development and commercialization of Orca-T. Provide medical and scientific information to the relevant teams of the organization, as well as guidance to Commercial/ Marketing Organizations on promotional material and campaigns. Requirements Educational requirements: Advanced life science [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
[. .. ] merit. Job Function: Legal Compliance Job Sub Function: Health Care Compliance Job Category: Professional All Job Posting Locations: Zug, Switzerland Job Description: The Health Care Compliance Leader [...]
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[...] for R D, Clinical Research, Medical Affairs and Business Development is a global leadership role responsible for the strategic oversight, design, and execution of an effective Health Care Compliance (HCC) program across Clinical Research, Medical Affairs, Research Development, and Business Development activities worldwide, including mergers, acquisitions, and strategic partnerships. This role reports directly to the Chief Compliance Officer, serves as a member of the Health Care Compliance Leadership Team, and acts as a trusted strategic advisor to senior R D, Medical Affairs, Clinical Operations, and Business Development leaders. The role is accountable for identifying, assessing, and mitigating compliance risks associated with innovation, external collaborations, and inorganic growth while [. .. ] Business Development activities, aligned to enterprise priorities and evolving risk profiles. Partner closely with Business partners to design, implement, and continuously enhance a robust, risk-based compliance program covering clinical trials, investigator and site interactions, research collaborations, scientific exchange, licensing, acquisitions, divestitures, and other strategic transactions. Act as a trusted compliance partner and advisor to R D, Clinical, Medical Affairs, and Business Development leaders, providing practical, forward-looking advice on novel business models, external collaborations, and strategic growth initiatives. Drive consistency, [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Zürich
Führungs-/ Leitungspositionen Homeoffice möglich
Chief Medical
Officer SJP Biotec Gmb H Vacant since : 01.09.2026 Number of jobs : 1 8001 Zürich (ZH) 100 Immediately Permanent SJP Biotec Gmb H is a
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[...] class=highlight_text>clinical-stage precision oncology company pioneering a first-in-class Selective Translation Regulatory Inhibitor (STRI) platform powered to overcome treatment resistance in refractory cancers. Founded in 2024, SJP targets RAS-driven, hormone-receptor-positive, and immune-refractory tumors with a novel pipeline of small molecules developed in our lab and ready to proceed with regulatory-grade
trials. Backed by a Scientific Advisory Board that includes world-leading authorities in RAS and breast cancer biology, and immuno-oncology, SJP has established clinical partnerships with leading medical centers world-wide including UCSF, NCI, MD Anderson, Baylor College of Medicine, MSKCC, and Mc Gill, to name a few. The Opportunity [. .. ]
▶ Zur Stellenanzeige
Job vor 14 Tagen bei Jobleads gefunden
• Bern
Führungs-/ Leitungspositionen
The Swiss Cancer Institute is the national network for
clinical cancer research in Switzerland. Since 1965, we have been committed to improving cancer treatment for the Swiss population as [...]
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[...] a non-profit organization. Guided by our vision Clinical research for a cure tomorrow, we conduct oncology clinical trials and serve as a key partner for authorities, professional associations, and the pharmaceutical industry. Approximately 70 employees at our Competence Center in Bern work closely with all leading oncology clinics across the country. As CSO, you will lead and further develop the Clinical Science Department (approximately 10 people) . You will shape and implement the scientific strategy of the institute, foster innovation and collaboration, and represent the organization nationally and internationally. Chief Scientific Officer CSO (80-100) Your tasks: Scientific Strategic Leadership: Lead the team that drives and implements the overall scientific strategy in close collaboration with physician-scientists from Swiss hospitals and universities, support study protocol development, ensure GCP and research quality, and serve as scientific spokesperson to authorities and partners. You will [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
• Bern
Führungs-/ Leitungspositionen
The Swiss Cancer Institute in Bern, Switzerland is seeking a Chief Scientific
Officer (CSO) to lead the
Clinical Science Department (10 people) and shape the institutes scientific strategy. [...]
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[...] You will oversee research quality, trial development, and collaboration with hospitals and academics. The CSO will drive investigator-initiated trials, foster innovation in oncology, build national and international partnerships, and represent the institute at major conferences. #J-18808-Ljbffr 02197945 [. .. ]
Job am 23.08.2026 bei Jobleads gefunden
Germany-Therapeutic Area Medical Lead-Oncology
• Frankfurt, Hesse
Summary The Therapeutic Area Lead Solid Tumors/ Pipeline is part of the Medical Affairs Team and provides a bridge between
Clinical Development, Medical Affairs, and the commercial organization at [...]
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[...] a senior mastery level. He/ she will be involved in a wide range of activities for inline and pipeline products. This is a very diverse role and a unique opportunity where you can cover the whole spectrum of drug development in various [. .. ] (e. g. , congress medical booth materials and planning) and participates in congress reporting and summaries Ensures the proper pre-medical and medical review of medical materials, serves as Information officer for all material related to solid tumors/ pipeline. Drives implementation of the medical/ non-promotional plans for respective products/ Gives medical input into local brand planning processes and to respective brand teams Ensures that HCP and educational activities are of high scientific quality and are in line with compliance regulations [. .. ] 5-7 years of relevant working experience in similar roles Proven track record in preparing for product launches and successful life cycle management Knowledge in development and implementation of clinical trials Experienced in material review in the role of an Information Officer Excellent communication skills and ability to present scientific data Structured approach to project management. Ability to work independently and effectively in complex, rapidly changing environments Analytical mind setting, entrepreneurial approach, hands-on Ability to travel up to 25 of [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Senior/ Executive Medical Director, Medical Lead IAI, Early Clinical Development
• Morges, Waadt
Führungs-/ Leitungspositionen
[. .. ] With a diverse and expanding early pipeline, Incyte is shaping the next generation of targeted and immune-based therapies. Our strength lies in our ability to combine scientific [...]
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[...] insight with clinical execution, transforming discoveries into impactful medicines for patients worldwide. We are a company in motion, growing, evolving, and investing in early development as a core engine of innovation. At Incyte, every idea begins with science, and every scientist plays a part in shaping what comes next. The role This position [. .. ] efforts for Incytes Dermatology, Immunology, Rheumatology products (preclinical candidate nomination through transition to registrational studies) Duties and Responsibilities Leads development efforts for assets post-candidate selection through first in human trials, including early dose escalation, ph 1-2a translational strategy (proof of mechanism studies) and proof of concept studies in human (ph 1b or 2a) . Participates in asset/ portfolio strategies and prioritization, internal and external messaging, governance, and cross-functional interface with all key stakeholders, including translational science, clinical pharmacology [. .. ] of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incytes data protection officer, and your supervisory authority (if applicable) . Please contact if you have any questions or concerns or would like to exercise your rights. #J-18808-Ljbffr 01460309 [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Therapeutic Area Medical Lead-Oncology-Sponsor dedicated (m/w/d)
• Frankfurt, Hesse
The Therapeutic Area Lead Solid Tumors/ Pipeline is part of the Medical Affairs Team and provides a bridge between
Clinical Development, Medical Affairs, and the commercial organization at a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] senior mastery level. He/ she will be involved in a wide range of activities for inline and pipeline products. This is a very diverse role and a unique opportunity where you can cover the whole spectrum of drug development in various [. .. ] (e. g. , congress medical booth materials and planning) and participates in congress reporting and summaries Ensures the proper pre-medical and medical review of medical materials, serves as Information officer for all material related to solid tumors/ pipeline. Drives implementation of the medical/ non-promotional plans for respective products/ Gives medical input into local brand planning processes and to respective brand teams Ensures that HCP and educational activities are of high scientific quality and are in line with compliance regulations [. .. ] 5-7 years of relevant working experience in similar roles Proven track record in preparing for product launches and successful life cycle management Knowledge in development and implementation of clinical trials Experienced in material review in the role of an Information Officer Excellent communication skills and ability to present scientific data Structured approach to project management. Ability to work independently and effectively in complex, rapidly changing environments Analytical mind setting, entrepreneurial approach, hands-on Ability to travel up to 25 of [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Chief Scientific Officer-Hybrid, Oncology Research Leader
• Bern
Führungs-/ Leitungspositionen
The Swiss Cancer Institute in Bern is seeking a Chief Scientific
Officer to lead its
Clinical Science Department and implement scientific strategies. The role entails fostering innovation, conducting [...]
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[...] clinical trials, and building partnerships to enhance cancer treatment research. The ideal candidate has a strong background in oncology or related life sciences and excels in project management and communication. A hybrid work model is offered for this full-time position. #J-18808-Ljbffr 01448801 [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Chief Scientific Officer (80-100)
• Bern
Führungs-/ Leitungspositionen
The Swiss Cancer Institute is the national network for
clinical cancer research in Switzerland. Since 1965, we have been committed to improving cancer treatment for the Swiss population as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a non-profit organization. Guided by our vision Clinical research for a cure tomorrow, we conduct oncology clinical trials and serve as a key partner for authorities, professional associations, and the pharmaceutical industry. Approximately 70 employees at our Competence Center in Bern work closely with all leading oncology clinics across the country. As CSO, you will lead and further develop the Clinical Science Department (approximately 10 people) . You will shape and implement the scientific strategy of the institute, foster innovation and collaboration, and represent the organization nationally and internationally. Chief Scientific Officer (80-100) Your tasks Scientific Strategic Leadership: Lead the team that drives and implements the overall scientific strategy in close collaboration with physician-scientists from Swiss hospitals and universities, support study protocol development, ensure GCP and research quality, and serve as scientific spokesperson to authorities and partners. You will oversee [. .. ]
Job am 18.08.2026 bei Jobleads gefunden
Assistant Director
Führungs-/ Leitungspositionen
[. .. ] the science practice of veterinary medicine to improve animal human health. Reporting to the Chief of Academic Affairs, Research Accreditation, the Assistant Director will perform functions to [...]
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[...] assist the Chief Officer to propose, develop implement AVMA policies programs concerning veterinary research, veterinary specialty board certification, specialists in academia, specialists in practice industry, the AVMA Veterinary Clinical Trials Registry. They will work closely with AVMA governance entities in the execution of duties. The Assistant Director will provide primary professional staff support for the Council on Research (COR) , the American Board of Veterinary Specialties (ABVS) , the Veterinary Specialty Organizations Committee (VSOC) , other governance entities as needed; [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Officer pro Jahr?
Als Clinical Trials Officer verdient man zwischen EUR 50.000,- bis EUR 75.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Officer Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 16 offene Stellenanzeigen für Clinical Trials Officer Jobs.
In welchen Bundesländern werden die meisten Clinical Trials Officer Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Officer Jobs werden derzeit in Niedersachsen (4 Jobs), Sachsen (2 Jobs) und Schleswig-Holstein (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Officer Jobs?
Clinical Trials Officer Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
