Merck & Co., Inc.
Global Associate Director Medical Affairs - Assets Cross Tumor and Innovative Strategies(m/w/x)
Full-timeWith HomeofficeExperienced
from USD 272,600 / year
Zürich
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TA
Takeda Development Center Americas, Inc.Associate Director, Global Regulatory Affairs, Advertising and Promotion(m/w/x)
Zürich
Full-timeWith Home OfficeSenior
Description
In this role, you will be the go-to expert for regulatory affairs in advertising and promotion, guiding the development and review of materials while ensuring compliance and patient safety. Your strategic insights will shape the product lifecycle from clinical trials to marketing, all while fostering teamwork and effective communication.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •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
Education
Bachelor's degree
Work Experience
8 years
Tasks
- •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
Languages
English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Takeda Development Center Americas, Inc. and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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TA
Takeda Development Center Americas, Inc.Associate Director, Global Regulatory Affairs, Advertising and Promotion(m/w/x)
Zürich
Full-timeWith Home OfficeSenior
New Job?Nejo!
The AI Job Search Engine
Description
In this role, you will be the go-to expert for regulatory affairs in advertising and promotion, guiding the development and review of materials while ensuring compliance and patient safety. Your strategic insights will shape the product lifecycle from clinical trials to marketing, all while fostering teamwork and effective communication.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •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
Education
Bachelor's degree
Work Experience
8 years
Tasks
- •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
Languages
English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Takeda Development Center Americas, Inc. and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Takeda Development Center Americas, Inc.
Industry
Pharmaceuticals
Description
The company is a patient-focused, R&D-driven global biopharmaceutical company committed to bringing Better Health and a Brighter Future to people worldwide.
Not a perfect match?
- Merck & Co., Inc.
Global Associate Director Medical Affairs - Assets Cross Tumor and Innovative Strategies(m/w/x)
Full-timeWith HomeofficeExperiencedfrom USD 272,600 / yearZürich - Takeda
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