Ida Sophie Grew

FAQ About Ida Sophie Grew

• What is Ida Sophie Grew's address?

  Ida Sophie Grew is located at
  Ferring Pharmaceuticals, Copenhagen, Denmark

• What is Ida Sophie Grew's job title?

  Ida Sophie Grew is a
  Ambitious Senior Director in Global Regulatory Affairs with an International Profile and Global Regulatory Project Lead expertise. People manager with a visionary and strategic mindset and strong communication skills as core enablers. + 10 years of experience working with global non-clinical and clinical drug development in a HQ capacity, with a passion for building global product development strategies and developing world-class organizations with processes that are fit the purpose. Started my career in Novo Nordisk in 2012 first as a Graduate in Regulatory Affairs and eventually as a Senior Professional and Global Regulatory Lead with responsibility for early drug development projects. Worked my way through various therapeutic areas in HQ in addition to two expat assignments in the US home office, while gaining experience with a variety of regulatory activities from early development to LCM. Have driven numerous regulatory submissions across EU, US and RoW, including sNDAs, CTAs, meeting packages, PIP/PSPs, and more, for biologics/biotechnology and drug products. Alongside my job I have boosted my professional competencies with a post-graduate education in Regulatory Affairs Medicines from the University of Hertfordshire in collaboration with TOPRA. Hold an undergraduate degree in Molecular Biomedicine (BSc) and a graduate degree in Pharmaceutical Sciences (MSc) from the University of Copenhagen, in both cases graduating in top 5% of class, and with solid theoretical and practical understanding of biomedical research. My dissertation was based on a clinical research project, independently performed at the Department of Clinical Pharmacology at Copenhagen Central Hospital. Specialties include: Global Regulatory Development and LCM Strategies, Regulatory Project Management, Global Drug Development and LCM Plans, Global Project Core Teams and Global Regulatory Project Teams, Regulatory risk assessments, US supplemental NDAs and labelling negotiations, US and EU pediatric plans, US device regulations, Scientific advice, HA interactions and Q&A, FDA meeting requests, FDA AdComm preparations, EU CTAs, China CTAs and NDAs Ferring Pharmaceuticals

• What industry does Ida Sophie Grew currently work in?

  Ida Sophie Grew currently works in the
  Ferring Pharmaceuticals

• What is Ida Sophie Grew's area of expertise?

  Ida Sophie Grew specializes in
  Ambitious Senior Director in Global Regulatory Affairs with an International Profile and Global Regulatory Project Lead expertise. People manager with a visionary and strategic mindset and strong communication skills as core enablers. + 10 years of experience working with global non-clinical and clinical drug development in a HQ capacity, with a passion for building global product development strategies and developing world-class organizations with processes that are fit the purpose. Started my career in Novo Nordisk in 2012 first as a Graduate in Regulatory Affairs and eventually as a Senior Professional and Global Regulatory Lead with responsibility for early drug development projects. Worked my way through various therapeutic areas in HQ in addition to two expat assignments in the US home office, while gaining experience with a variety of regulatory activities from early development to LCM. Have driven numerous regulatory submissions across EU, US and RoW, including sNDAs, CTAs, meeting packages, PIP/PSPs, and more, for biologics/biotechnology and drug products. Alongside my job I have boosted my professional competencies with a post-graduate education in Regulatory Affairs Medicines from the University of Hertfordshire in collaboration with TOPRA. Hold an undergraduate degree in Molecular Biomedicine (BSc) and a graduate degree in Pharmaceutical Sciences (MSc) from the University of Copenhagen, in both cases graduating in top 5% of class, and with solid theoretical and practical understanding of biomedical research. My dissertation was based on a clinical research project, independently performed at the Department of Clinical Pharmacology at Copenhagen Central Hospital. Specialties include: Global Regulatory Development and LCM Strategies, Regulatory Project Management, Global Drug Development and LCM Plans, Global Project Core Teams and Global Regulatory Project Teams, Regulatory risk assessments, US supplemental NDAs and labelling negotiations, US and EU pediatric plans, US device regulations, Scientific advice, HA interactions and Q&A, FDA meeting requests, FDA AdComm preparations, EU CTAs, China CTAs and NDAs

• Which languages does Ida Sophie Grew speak? 

  Ida Sophie Grew speaks the following languages:
  No languages available.

• Which industries has Ida Sophie Grew previously worked in?   

  Ida Sophie Grew has prior experience in the following industries:
  Ferring Pharmaceuticals , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk , Copenhagen Central Hospital , Lundbeck , Department Of Biology Faculty Of Science University Of Copenhagen , Deloitte

• What is Ida Sophie Grew’s work experience?  

  Ida Sophie Grew has the following professional experience:
  Ferring Pharmaceuticals , Ferring Pharmaceuticals , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk , Novo Nordisk , Copenhagen Central Hospital , Lundbeck , Department Of Biology Faculty Of Science University Of Copenhagen , Deloitte .

• How can I find Ida Sophie Grew on LinkedIn?  

  You can view Ida Sophie Grew’s
  LinkedIn profile at LinkedIn URL.

• What are Ida Sophie Grew’s work email addresses?  

  Ida Sophie Grew’s work email addresses are
  [email protected] .

• What company does Ida Sophie Grew work for?  

  Ida Sophie Grew works at
  Ferring Pharmaceuticals