Associate Director, Global Regulatory Affairs, Advertising and Promotion
Takeda
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇨🇭 Switzerland
Visit company websiteJob Level
Senior
About the role
- Act as the Subject Matter Expert for assigned products and projects focusing on advertising and promotion regulatory affairs.
- Provide regulatory guidance during development, review, approval, and implementation of medical and commercial materials.
- Serve as product or project business lead for global CMRP at Takeda CMRP Meeting Chair.
- Strategic business partner from clinical trial development through the marketing maintenance phase of a product lifecycle.
- Exercise decision-making authority within the CMRP to ensure compliance, patient safety, and alignment with Takeda’s values.
Requirements
- BSc Degree, preferred. BA accepted.
- 8+ years of pharmaceutical industry experience.
- 6 years of regulatory experience or combination of 5+ years regulatory and/or related experience.
- Ability to understand ABPI, EFPIA and other international code and guidance about advertising and promotion for prescription medicines.
- Experience in prescription medicine promotion development and review process.
- Strong interpersonal skills with ability to demonstrate strategic and analytic thinking.
- Demonstrated ability to communicate clearly and concisely.
- Highly effective written and verbal communication skills to manage, motivate and drive decisions within teams.
- Proven skills in negotiation, influencing without authority and working diplomatically through conflict.
- Demonstrated cross-functional people management with a desire to foster a positive team culture.
- Ability to work independently, take initiative and complete tasks to deadlines.
- Previous experience in an advertising and promotion role.
- Proven experience and expertise in regulatory affairs, particularly advertising and promotion, with familiarity in EFPIA, IFPMA, and FDA standards.
- Strong leadership, negotiation, and conflict resolution skills within cross-functional teams.
- Strategic mindset and ability to assess and advise regulatory impacts across the product lifecycle.
- Adept in guiding teams through complex advertising and promotion processes with a focus on patient safety and compliance.
Benefits
- Health insurance
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
regulatory affairsadvertising and promotionclinical trial developmentproduct lifecycle managementcompliancepatient safetyprescription medicine promotionnegotiationinfluencing without authoritycross-functional people management
Soft skills
interpersonal skillsstrategic thinkinganalytic thinkingclear communicationwritten communicationverbal communicationconflict resolutionteam culture fosteringindependenceinitiative
Certifications
BSc DegreeBA Degree