Protocol Specialist Stellenangebote


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Stellenangebote Protocol Specialist Jobs bei Mindmatch.ai


Neu Job vor 10 Std. gefunden Pharmiweb

Executive Director Clinical Development

Führungs-/ Leitungspositionen
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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
MEHR[...] Data sheet, Annual Safety Report/ IND Safety Reports, preparation for the Milestones Start of Development, Proof of Clinical Principle, Release of Full Development, Release of Submission. You provide medical oversight to the clinical trial program within your respective project during protocol development, conduct, analysis and reporting, and you have responsibility for continuous benefit- risk assessment. You also oversee medical project budgets [...] 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 Protocol Specialist Jobs gefunden bei Jobbörse Jobleads

Stellenangebote Protocol Specialist Jobs bei Jobleads


Job vom 09.12.2024 Leiter Softwareentwicklung • Stuttgart, Baden- Württemberg Führungs-/ Leitungspositionen
MEHR[...] Nachhaltigkeitsmanagement mit Schwerpunkt ESG/ CSRD Reporting Location: Germany, Munich Salary: Competitive Salary Project Manager, Factory Construction and Facility Location: Malaysia, Johor Bahru Salary: Competitive Salary Category Manager Software und IT/ Strategischer Einkäufer (m/w/d) Location: Germany, Leipzig Salary: Competitive Salary HR Specialist Location: China, Beijing Salary: Competitive Salary Cashier Location: China, Beijing Salary: Competitive Salary R D C++ Protocol L2 Engineer Location: China, Beijing Salary: Competitive Salary Bachelorand (m/w/d) für Datenbankentwicklung und Automatisierung im Bereich NAVY Systeme Location: Germany, [...]
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Stellenangebote Protocol Specialist Jobs gefunden bei Jobbörse StepStone

Stellenangebote Protocol Specialist Jobs bei StepStone


Job vom 17.12.2024 Interroll Holding GmbH

Corporate Sustainability Specialist (m/w/d)

• Sinsheim Beratungs-/ Consultingtätigkeiten Homeoffice möglich 30+ Urlaubstage
MEHR[...] 35 Unternehmen mit einem Umsatz von CHF 556. 3 Millionen und rund 2400 Mitarbeitenden (durchschnittlicher Personalbestand in 2023) . Entwicklung eines umfassenden globalen (Klima- ) Berichtswesens unter Berücksichtigung von Gesetzgebungen und internationalen Standards wie CSRD/ ESRS E1, TCFD und GHG- Protocol. Implementierung von standardisierten Methoden zur Berechnung und Berichterstattung der Unternehmens- Treibhausgas- Bilanz (Scope- 1,- 2 und- 3 Emissionen) . Aufbau [...] die Innovationskraft zu steigern Viele zusätzliche Benefits: Jobrad, einen Parkplatz stellen wir kostenlos zur Verfügung, vergünstiges Mittagessen, etc. 30 Tage Urlaub Flexible Gestaltung von mobile Office und vor Ort Arbeit . Interroll Holding GmbH sucht in Sinsheim eine/n Corporate Sustainability Specialist (m/w/d) (ID- Nummer: 11831018) 26819739 [...]
Stellenangebot Protocol Specialist Job bei Edwards Lifesciences Services GmbH Job vom 11.12.2024 Edwards Lifesciences Services GmbH Therapy Activation Specialist IMAGING, TMTT- EVOQUE- experience as Application Specialist with cardiac imaging knowledge very welcome • bundesweit Homeoffice möglich
MEHR[...] clinical baseline, procedural, and follow- up imaging (e. g. , CT, echo, MRI, angiography) to provide inputs that support new product and procedure development and to support event investigations Collaborate with HCPs to develop imaging patient selection criteria and screening protocol Train field support team and/ or HCPs on cardiac imaging procedures Provide on- site cardiac imaging support and guidance during [...] Other incidental duties What youll need (Required) : Minimum 3 years experience in medical device and/ or clinical experience (clinical physiology, echocardiography) Similar Industry certification (Imaging- TTE- transthoracic echocardiogram) or previous edge to edge therapy experience or experience as Application Specialist working for manufacturer of CT/ Echo machines Fluent/ Advanced in English. German is big advantage (we are ready to support [...]
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Job vor 11 Tagen gefunden Interroll Holding GmbH

Sustainability Specialist- Germany (m/w/d)

• Sinsheim Homeoffice möglich 30+ Urlaubstage
MEHR[...] 35 Unternehmen mit einem Umsatz von CHF 556. 3 Millionen und rund 2400 Mitarbeitenden (durchschnittlicher Personalbestand in 2023) . Verantwortung des Nachhaltigkeitsmanagements an den Interroll Standorten in Sinsheim und Obrigheim Umsetzung der relevanten Berichtsstandards nach CSRD, GRI, TCFD und GHG- Protocol an beiden Standorten Beratung des Managements und der Mitarbeiter der beiden Interroll Standorte in Sinsheim und Obrigheim bei allen Fragen [...] und die Innovationskraft zu steigern Viele zusätzliche Benefits: Jobrad, einen Parkplatz stellen wir kostenlos zur Verfügung, vergünstiges Mittagessen, etc. 30 Tage Urlaub Flexible Gestaltung von mobile Office und vor Ort Arbeit . Interroll Holding GmbH sucht in Sinsheim eine/n Sustainability Specialist- Germany (m/w/d) (ID- Nummer: 11831256) 27455772 [...]
Stellenangebot Protocol Specialist Job bei ENERCON Job vom 19.11.2024 ENERCON Sustainability Specialist Corporate Carbon Accounting (m/w/d) • Bremen, bundesweit Homeoffice möglich Abgeschlossenes Studium Flexible Arbeitszeiten 30+ Urlaubstage
MEHR[...] und Unternehmensberatung Mehrjährige Expertise hinsichtlich Corporate Carbon Accounting, der Festlegung von Science- Based Targets, der Umsetzung von Aktions plänen zur Dekarboni sierung oder in ver wandten Bereichen sowie Know- how in Bezug auf einschlägige Standards und Initiativen (z. B. GHG Protocol, Science- Based- Targets- Initiative, ESRS) Routinierter Umgang mit MS Office, insbe sondere Excel, einschließ lich Makros und VBA Sehr gute [...] Private Berufs unfähigkeits versicherung zu speziellen Konditionen Spannende und abwechslungsreiche Tätigkeiten in der grünen Wachstums branche Windenergie Finde mehr über Deine individuellen Benefits heraus Deine zukünftige Personal abteilung hilft Dir gerne dabei. . ENERCON sucht in Bremen, bundesweit eine/n Sustainability Specialist Corporate Carbon Accounting (m/w/d) (ID- Nummer: 11712309) 20872264 [...]
Stellenangebot Protocol Specialist Job bei Edwards Lifesciences Services GmbH Job vom 08.11.2024 Edwards Lifesciences Services GmbH Commercial Field Clinical Specialist Imaging PASCAL- experience as Application Specialist with cardiac imaging knowledge very welcome • bundesweit Beratungs-/ Consultingtätigkeiten Homeoffice möglich
MEHR[...] here and furthermore we are offering also Pascal ACE (very thin Pascal) . Every patient is different- be an expert on all ECHOCARDIOGRAPHY elements about our PASCAL device/ therapy and help many patients suffering with regurgitation The Commercial Field Clinical Specialist Imaging PASCAL is responsible for education physician on all echocardiography aspects and case support in assigned territories/ regions. Requested candidate [...] clinical baseline, procedural, and follow- up imaging (e. g. , CT, echo, MRI, angiography) to provide inputs that support new product and procedure development and to support event investigations Collaborate with HCPs to develop imaging patient selection criteria and screening protocol Train field support team and/ or HCPs on cardiac imaging procedures Provide on- site cardiac imaging support and guidance during [...]
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