Descrizione dell'offerta
Key Responsibilities
Drive the regulatory strategy, planning and execution across key regions for the assigned development pipeline projects (from early pre‑clinical phases) Collaborate with cross‑functional teams to ensure timely submissions, approvals, and compliance with global regulatory requirements, supporting the successful development and registration of innovative pharmaceutical products Develop and implement global regulatory strategies for assigned pipeline development programs, ensuring alignment with global regulatory requirements and company objectives Provide regulatory input into R&D programs to ensure they meet regulatory expectations Prepare, review, and manage regulatory submissions including INDs, NDAs, MAAs, ensuring accuracy, completeness, and timely delivery Coordinate responses to health authority queries, ensuring scientifically sound and compliant answers within required timelines Monitor evolving regulatory requirements across major markets (FDA, EMA, ICH) and proactively assess their impact on development programs and submission strategies Collaborate with cross‑functional teams (R&D, Clinical Development, CMC, Safety, Quality, business etc.) to ensure integrated regulatory plans Support regulatory meetings and interactions with health authorities, including briefing document preparation Ensure compliance with internal SOPs and global standards, contributing to continuous improvement initiatives and best practices in regulatory operations Review and approve Clinical Trials Applications (CTAs) Perform regulatory due diligence activities for acquisition of new assets in development stages to enhance company pipeline Experience / Professional requirement
More than 5 years of successful managerial experience in the pharmaceutical industry with a proven track record of successful registrations of innovative products in key regions (EU, US, Japan) Strong knowledge of regulatory submission and approval processes in key regions Strong knowledge of drug development & regulatory processes behind with a focus on early‑stage assets Experience leading regulatory submissions and approvals of innovative products Key Regions Experience in a global/matrix environment or cross‑functional teams in the pharmaceutical industry Experience on project allocation/project planning within a cross‑functional team working in matrix organization Excellent interpersonal, communication, negotiation and problem‑solving skills Organizational awareness (interrelationship of departments, business priorities) Fluency in English as a business language Excellent written and verbal communication skills Confident, articulate, and professional speaking abilities (and experience) Excellent presentation and negotiation skills Initial Salary
64.000 € Angelini Pharma is an Equal Opportunity Employer. We believe that diversity is a huge value that contributes to individual and company success. We are committed to create and foster a diverse and inclusive environment.
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Drive the regulatory strategy, planning and execution across key regions for the assigned development pipeline projects (from early pre‑clinical phases) Collaborate with cross‑functional teams to ensure timely submissions, approvals, and compliance with global regulatory requirements, supporting the successful development and registration of innovative pharmaceutical products Develop and implement global regulatory strategies for assigned pipeline development programs, ensuring alignment with global regulatory requirements and company objectives Provide regulatory input into R&D programs to ensure they meet regulatory expectations Prepare, review, and manage regulatory submissions including INDs, NDAs, MAAs, ensuring accuracy, completeness, and timely delivery Coordinate responses to health authority queries, ensuring scientifically sound and compliant answers within required timelines Monitor evolving regulatory requirements across major markets (FDA, EMA, ICH) and proactively assess their impact on development programs and submission strategies Collaborate with cross‑functional teams (R&D, Clinical Development, CMC, Safety, Quality, business etc.) to ensure integrated regulatory plans Support regulatory meetings and interactions with health authorities, including briefing document preparation Ensure compliance with internal SOPs and global standards, contributing to continuous improvement initiatives and best practices in regulatory operations Review and approve Clinical Trials Applications (CTAs) Perform regulatory due diligence activities for acquisition of new assets in development stages to enhance company pipeline Experience / Professional requirement
More than 5 years of successful managerial experience in the pharmaceutical industry with a proven track record of successful registrations of innovative products in key regions (EU, US, Japan) Strong knowledge of regulatory submission and approval processes in key regions Strong knowledge of drug development & regulatory processes behind with a focus on early‑stage assets Experience leading regulatory submissions and approvals of innovative products Key Regions Experience in a global/matrix environment or cross‑functional teams in the pharmaceutical industry Experience on project allocation/project planning within a cross‑functional team working in matrix organization Excellent interpersonal, communication, negotiation and problem‑solving skills Organizational awareness (interrelationship of departments, business priorities) Fluency in English as a business language Excellent written and verbal communication skills Confident, articulate, and professional speaking abilities (and experience) Excellent presentation and negotiation skills Initial Salary
64.000 € Angelini Pharma is an Equal Opportunity Employer. We believe that diversity is a huge value that contributes to individual and company success. We are committed to create and foster a diverse and inclusive environment.
#J-18808-Ljbffr
Candidatura e Ritorno (in fondo)
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