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International Diplomacy Specialist 21 Jobs International Trade Specialist 288 Jobs International Affairs 16 Jobs Diplomacy 176 Jobs Foreign Relations 82 Jobs

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214 Stellenangebote


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Stellenangebot International Affairs Specialist Job bei ZEISS Job vom 17.12.2024 ZEISS

Regulatory/ Clinical Affairs (RA/ CA) Team Lead (m/f/x)

 • Jena Führungs-/ Leitungspositionen Beratungs-/ Consultingtätigkeiten
MEHR[...] to function optimally. Medical technology from ZEISS supports medical professionals in improving the lives of patients worldwide. The fact that our actions have a direct impact on peoples well- being is what drives us every day. Your Role You are specialist and disciplinary manager of the Regulatory and Clinical Affairs department of one or more product lines in the respective division (BS) You are overseeing a team with an emphasis [...] with interface departments and guarantee increased value to our specialty department. Completed natural science or technical studies with bachelor or masters degree (or corresponding professional experience) Significant professional background, which includes experience in regulatory/ clinical fields. Relevant expertise in the international product registration of Class I to Class III medical devices Proven leadership and team management skills within international, inter- cultural [...]
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Stellenangebote International Affairs Specialist Jobs bei Mindmatch.ai


Neu Job vor 10 Std. gefunden Pharmiweb Executive Director Clinical Development Führungs-/ Leitungspositionen
MEHRJob Description Job Title: Executive Director Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb

VP Clinical Development

 • Leipzig, SN
MEHRJob Description Job Title: VP Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb VP Clinical Development • Düsseldorf, NW
MEHRJob Description Job Title: VP Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb

Executive Director Clinical Development

 • Munich, BY Führungs-/ Leitungspositionen
MEHRJob Description Job Title: Executive Director Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb Executive Director Clinical Development • Cologne, NW Führungs-/ Leitungspositionen
MEHRJob Description Job Title: Executive Director Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb VP Clinical Development • Frankfurt
MEHRJob Description Job Title: VP Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb Executive Director Clinical Development • Frankfurt Führungs-/ Leitungspositionen
MEHRJob Description Job Title: Executive Director Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb Executive Director Clinical Development • Hamburg, HH Führungs-/ Leitungspositionen
MEHRJob Description Job Title: Executive Director Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb Executive Director Clinical Development • Essen, NW Führungs-/ Leitungspositionen
MEHRJob Description Job Title: Executive Director Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb Executive Director Clinical Development • Leipzig, SN Führungs-/ Leitungspositionen
MEHRJob Description Job Title: Executive Director Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb VP Clinical Development • Dortmund, NW
MEHRJob Description Job Title: VP Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb Executive Director Clinical Development • Dortmund, NW Führungs-/ Leitungspositionen
MEHRJob Description Job Title: Executive Director Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb VP Clinical Development • Berlin, BE
MEHRJob Description Job Title: VP Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb VP Clinical Development • Stuttgart, BW
MEHRJob Description Job Title: VP Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
Job vom 15.12.2024 Pharmiweb VP Clinical Development • Essen, NW
MEHRJob Description Job Title: VP Clinical Development- Oncology Tasks responsibilities In this role, you represent Medicine at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: definition of Target Product Profiles, [...] Data Monitoring boards. In addition, you provide medical leadership in regulatory meetings and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product Maintenance and Optimization Summary. Furthermore, you review and approve publications within [...] asset (s) , e. g. Health Authorities, Key External Experts, Associations, Patient groups, Payers, among others. You oversee and support all contacts to external experts, executive/ steering committees, adjudication committees and Safety Data Monitoring boards for your projects. Requirements MD (specialist in Oncology or equivalent) with sound clinical oncology experience and (ideally) some years of experience in the pharmaceutical industry Successful [...]
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Stellenangebote International Affairs Specialist Jobs gefunden bei Jobbörse Neuvoo.com

Stellenangebote International Affairs Specialist Jobs bei Neuvoo.com


Stellenangebot International Affairs Specialist Job bei Mesa Germany GmbH Job vom 18.12.2024 Mesa Germany GmbH

Quality Management/ Regulatory Affairs Specialist (m/f/d)

 • Waldems
MEHR[...] using our skills to serve a greater purpose. We approach each day with a unique, customer- focused vision to protect the vulnerable and empower every employee to make a real difference. Make your difference in Waldems as Quality Management/ Regulatory Affairs Specialist (m/f/d) The Quality Management/ Regulatory Affairs Specialist is responsible for supporting the quality assurance and regulatory affairs processes within the [...] they meet established high quality standards and legal requirements. Assists in the documentation and quality improvement initiatives. Duties/ Responsibilities: Creation and Evaluation: Collaborate in the establishment, implementation, maintenance and improvement of a quality management system in accordance with national and international standards and regulations. Identify defects or issues and work with the development team to ensure resolution. Documentation and Reporting: Assist [...]
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Stellenangebote International Affairs Specialist Jobs gefunden bei Jobbörse Mindmatch.ai

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Stellenangebot International Affairs Specialist Job bei Human Optics Holding AG Neu Job vor 10 Std. gefunden Human Optics Holding AG Regulatory Affairs Specialist (m/w/d) • Erlangen, BY Abgeschlossenes Studium 30+ Urlaubstage
MEHRAls innovativer und international ausgerichteter Hersteller von Premium- Implantaten für die Augenchirurgie entwickeln, produzieren und vertreiben wir Medizinprodukte, um dem menschlichen Auge die bestmögliche Sehkraft zurückzugeben. Zur Verstärkung unseres Teams am Standort Erlangen suchen wir zum nächstmöglichen Zeitpunkt in Vollzeit einen Regulatory Affairs Specialist (m/w/d) IHRE AUFGABEN Zulassung und Registrierung von Medizinprodukten in nationalen und internationalen Märkten Vorbereitung von Unterlagen für die Beglaubigung und [...]
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Stellenangebote International Affairs Specialist Jobs gefunden bei Jobbörse JobMESH

Stellenangebote International Affairs Specialist Jobs bei JobMESH


Job vor 8 Tagen gefunden PAJUNK GmbH Medizintechnologie

Clinical Evaluation Specialist (m/w/d)

 • Baden- Württemberg Abgeschlossenes Studium Flexible Arbeitszeiten Betriebliche Altersvorsorge
MEHRTogether into the future Pajunk ist ein international agierendes und inhabergeführtes Unternehmen mit Hauptsitz in Geisingen in Süddeutschland und Vertriebsniederlassungen in den USA, Großbritannien und der Schweiz. Wir [...] Schmerztherapie, Neurologie, Biopsie sowie der minimalinvasiven Chirurgie. Der Pioniergeist hat uns von Anfang an getrieben. Damit Innovation immer Tradition bleibt, suchen wir Menschen die neuen Aufgaben mit Innovation und Kreativität begegnen. Unterstützen Sie unser Team ab sofort als Clinical Evaluation Specialist (m/w/d) an unserem Standort in Geisingen. Ihre Aufgaben: Klinische Bewertungen erstellen, überarbeiten und pflegen Review von Produktbroschüren und Gebrauchsanweisungen für klinische Belange erarbeiten Wissenschaftliche Literatur als Input für die Abteilungen Marketing und Entwicklung recherchieren, auswerten und darstellen Klinische Zulassungsstrategie in Zusammenarbeit mit der Abteilung Regulatory Affairs erarbeiten Risikobewertungen in Abstimmung mit dem Qualitätsmanagement durchführen Prozesse einhalten und verbessern Ihr Profil: Erfolgreich abgeschlossenes Studium im Bereich Ingenieurwesen, [...]
Job vom 18.12.2024 Mesa Germany GmbH Quality Management/ Regulatory Affairs Specialist (m/f/d) • Hessen
MEHR[...] using our skills to serve a greater purpose. We approach each day with a unique, customer- focused vision to protect the vulnerable and empower every employee to make a real difference. Make your difference in Waldems as Quality Management/ Regulatory Affairs Specialist (m/f/d) The Quality Management/ Regulatory Affairs Specialist is responsible for supporting the quality assurance and regulatory affairs processes within the [...] they meet established high quality standards and legal requirements. Assists in the documentation and quality improvement initiatives. Duties/ Responsibilities: Creation and Evaluation: Collaborate in the establishment, implementation, maintenance and improvement of a quality management system in accordance with national and international standards and regulations. Identify defects or issues and work with the development team to ensure resolution. Documentation and Reporting: Assist [...]
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Stellenangebote International Affairs Specialist Jobs gefunden bei Jobbörse Stellenanzeigen.de

Stellenangebote International Affairs Specialist Jobs bei Stellenanzeigen.de


Stellenangebot International Affairs Specialist Job bei Mesa Germany GmbH Job vom 17.12.2024 Mesa Germany GmbH Quality Management/ Regulatory Affairs Specialist (m/f/d) • 65529, Waldems, Deutschland
MEHR[...] using our skills to serve a greater purpose. We approach each day with a unique, customer- focused vision to protect the vulnerable and empower every employee to make a real difference. Make your difference in Waldems as Quality Management/ Regulatory Affairs Specialist (m/f/d) The Quality Management/ Regulatory Affairs Specialist is responsible for supporting the quality assurance and regulatory affairs processes within the [...] they meet established high quality standards and legal requirements. Assists in the documentation and quality improvement initiatives. Duties/ Responsibilities: Creation and Evaluation: Collaborate in the establishment, implementation, maintenance and improvement of a quality management system in accordance with national and international standards and regulations. Identify defects or issues and work with the development team to ensure resolution. Documentation and Reporting: Assist [...]
Stellenangebot International Affairs Specialist Job bei Human Optics Holding AG Job vom 20.10.2024 Human Optics Holding AG Regulatory Affairs Specialist (m/w/d) • 91054, Erlangen, Deutschland Abgeschlossenes Studium 30+ Urlaubstage
MEHRAls innovativer und international ausgerichteter Hersteller von Premium- Implantaten für die Augenchirurgie entwickeln, produzieren und vertreiben wir Medizinprodukte, um dem menschlichen Auge die bestmögliche Sehkraft zurückzugeben. Zur Verstärkung unseres Teams am Standort Erlangen suchen wir zum nächstmöglichen Zeitpunkt in Vollzeit einen Regulatory Affairs Specialist (m/w/d) IHRE AUFGABEN Zulassung und Registrierung von Medizinprodukten in nationalen und internationalen Märkten Vorbereitung von Unterlagen für die Beglaubigung und [...]
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Job vor 12 Tagen gefunden Vice President, Regulatory Compliance Product Safety (New York) Führungs-/ Leitungspositionen
MEHR[...] Responsibilities: Formalize and document OLAPLEXs regulatory compliance and product safety testing program, including policies, procedures, and other related documentation, to ensure evidence adherence to and alignment with global laws, regulations, and industry standards. Proactively report on emerging developments and regulatory affairs via an effective global surveillance program, including the introduction of new legislation that is important to OLAPLEXs strategic decisions. Partner [...] safety guidance for usage/ country/ percentage. Oversee and participate in country registration with distributors and third- party certifiers. Oversee and participate in reviewing, revising, and approving artwork and marketing materials to ensure global regulatory compliance. Lead and develop Regulatory Affairs Specialist and Sr. Manager Product Safety team members. Represent OLAPLEX at various industry trade associations (e. g. , PCPC) to ensure proper knowledge of and representation on scientific, regulatory, and international matters. Report findings to cross- functional team members on a regular basis. Oversee and lead OLAPLEXS adverse event reporting program, [...]
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Job vom 25.11.2024 Head of Trading Compliance (d/ f/m) • Karlsruhe, Baden- Württemberg Führungs-/ Leitungspositionen
MEHR[...] an experienced Compliance Manager for our Trading business unit. In this role, you will work closely with EnBW s central Compliance function to further develop and optimize the existing compliance management system to ensure we meet all our local and international compliance requirements. You will actively contribute to the development of compliance structures specific or particularly relevant for Trading, for example [...] to adapt to our changing business requirements. Monitor regulatory compliance in the area of algo trading. Monitor compliance with respect to regulatory reporting (MiFID, REMIT, MAR) and ESG reporting. Work with internal stakeholders, in particular Legal and Market Design Regulatory Affairs, to analyze and evaluate suspicious cases, new requirements and risks, and develop appropriate solutions. Perform compliance risk assessments and provide regular reports on compliance risks and compliance breaches to senior management and relevant stakeholders. Train and sensitize employees on compliance issues and promote a culture of compliance. Team responsibility: Lead a small, specialist compliance team focused on international and local regulatory compliance. You will manage the team through regular feedback and development meetings, [...]
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* Verwandte Jobs
International Diplomacy Specialist 21 Jobs International Trade Specialist 288 Jobs International Affairs 16 Jobs Diplomacy 176 Jobs Foreign Relations 82 Jobs

Weitere Job-Ideen!
International Officer 25 Jobs Payment Operations Specialist 10 Jobs Internationaler Business Manager 7 Jobs Fixed Income Manager 6 Jobs

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