Merck & Co., Inc., Rahway, NJ, USA
Associate Director – Global Market Access – Sustainable Access Solutions(m/w/x)
Vollzeitmit HomeofficeSenior
Zürich
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
TATakeda Development Center Americas, Inc.
Associate Director, Global Regulatory Affairs, Advertising and Promotion(m/w/x)
Zürich
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Regulatory guidance for global advertising and promotion materials, leading CMRP reviews for assigned products at an R&D-driven biopharmaceutical company. 8+ years pharmaceutical industry experience, 6+ years regulatory experience, and ABPI/EFPIA advertising codes knowledge required. Global project leadership for regulatory review processes.
Anforderungen
- BSc Degree or BA
- 8+ years of pharmaceutical industry experience
- 6 years of regulatory experience or 5+ years regulatory and/or related experience
- Understanding of ABPI, EFPIA and international advertising codes
- Experience in prescription medicine promotion development
- Strong interpersonal skills
- Ability to communicate clearly and concisely
- Effective written and verbal communication skills
- Proven negotiation and influencing skills
- Cross-functional people management skills
- Ability to work independently and meet deadlines
- Previous experience in advertising and promotion role
- Experience in regulatory affairs, particularly advertising and promotion
- Strong leadership and conflict resolution skills
- Strategic mindset for regulatory impacts assessment
- Guiding teams through advertising and promotion processes
Aufgaben
- Act as the Subject Matter Expert for assigned products and projects
- Provide regulatory guidance during the development and review of medical and commercial materials
- Serve as the Regulatory Advisor in the Medical, Legal, and Regulatory review process
- Lead global CMRP as the product or project business lead
- Chair CMRP meetings and facilitate communication among team members
- Negotiate and resolve team disputes while maintaining focus on patient needs
- Oversee escalation steps for alignment on new data or campaigns
- Partner strategically from clinical trial development through product marketing
- Provide expertise on EFPIA, IFPMA, and FDA codes and regulations
- Ensure compliance and patient safety within the CMRP
- Lead and motivate team members to achieve organizational goals
- Identify and implement processes for reviewing promotional materials
- Advocate for and implement positive change within the organization
- Analyze complex issues and propose effective solutions
- Communicate clearly and concisely in all interactions
- Adapt to various personalities to foster goal achievement
- Collaborate effectively in a cross-functional team environment
- Create and deliver impactful presentations with focused recommendations
Berufserfahrung
- 8 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Takeda Development Center Americas, Inc. erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
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Vollzeitmit HomeofficeSeniorBaar
TATakeda Development Center Americas, Inc.
Associate Director, Global Regulatory Affairs, Advertising and Promotion(m/w/x)
Zürich
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Regulatory guidance for global advertising and promotion materials, leading CMRP reviews for assigned products at an R&D-driven biopharmaceutical company. 8+ years pharmaceutical industry experience, 6+ years regulatory experience, and ABPI/EFPIA advertising codes knowledge required. Global project leadership for regulatory review processes.
Anforderungen
- BSc Degree or BA
- 8+ years of pharmaceutical industry experience
- 6 years of regulatory experience or 5+ years regulatory and/or related experience
- Understanding of ABPI, EFPIA and international advertising codes
- Experience in prescription medicine promotion development
- Strong interpersonal skills
- Ability to communicate clearly and concisely
- Effective written and verbal communication skills
- Proven negotiation and influencing skills
- Cross-functional people management skills
- Ability to work independently and meet deadlines
- Previous experience in advertising and promotion role
- Experience in regulatory affairs, particularly advertising and promotion
- Strong leadership and conflict resolution skills
- Strategic mindset for regulatory impacts assessment
- Guiding teams through advertising and promotion processes
Aufgaben
- Act as the Subject Matter Expert for assigned products and projects
- Provide regulatory guidance during the development and review of medical and commercial materials
- Serve as the Regulatory Advisor in the Medical, Legal, and Regulatory review process
- Lead global CMRP as the product or project business lead
- Chair CMRP meetings and facilitate communication among team members
- Negotiate and resolve team disputes while maintaining focus on patient needs
- Oversee escalation steps for alignment on new data or campaigns
- Partner strategically from clinical trial development through product marketing
- Provide expertise on EFPIA, IFPMA, and FDA codes and regulations
- Ensure compliance and patient safety within the CMRP
- Lead and motivate team members to achieve organizational goals
- Identify and implement processes for reviewing promotional materials
- Advocate for and implement positive change within the organization
- Analyze complex issues and propose effective solutions
- Communicate clearly and concisely in all interactions
- Adapt to various personalities to foster goal achievement
- Collaborate effectively in a cross-functional team environment
- Create and deliver impactful presentations with focused recommendations
Berufserfahrung
- 8 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Takeda Development Center Americas, Inc. erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Über das Unternehmen
Takeda Development Center Americas, Inc.
Branche
Pharmaceuticals
Beschreibung
The company is a patient-focused, R&D-driven global biopharmaceutical company committed to bringing Better Health and a Brighter Future to people worldwide.
Noch nicht perfekt?
- Merck & Co., Inc., Rahway, NJ, USA
Associate Director – Global Market Access – Sustainable Access Solutions(m/w/x)
Vollzeitmit HomeofficeSeniorZürich - Takeda
Process Engineer Small Molecules API Process Science (Associate Director)(m/w/x)
Vollzeitmit HomeofficeSeniorZürich - CSL Behring
Senior Counsel, CMO & Global Supply Chain(m/w/x)
Vollzeitmit HomeofficeSeniorBern, Zürich, Sankt Gallen - ICON plc
Senior Specialist - Medical Information(m/w/x)
VollzeitRemoteSeniorZürich - AstraZeneca
Senior Specialist Marketing Operations Quality(m/w/x)
Vollzeitmit HomeofficeSeniorBaar