Regulatory Affairs Lead – EU & Global Submissions (GRD)

Iqvia Italia; Trieste/Trst; In loco; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading global pharmaceutical company is looking for a Regulatory Affairs Manager to develop strategies and manage regulatory submissions for Emerging Markets. The ideal candidate will have 3 to 5 years of experience in regulatory affairs, a Life Science degree, and strong communication skills. This role offers a challenging environment where you will work both independently and as part of a team.

Competenze

• 3 to 5 years of experience in corporate regulatory affairs roles.
• In-depth knowledge in drug development.
• Experience in leadership and coaching is a plus.

Mansioni

• Develop regulatory strategies for Emerging Markets.
• Manage regulatory submissions throughout product life cycles.
• Advise on regional regulatory requirements.

Conoscenze

Regulatory strategies development

Collaboration with consultants and partners

Regulatory requirements knowledge

Written and oral communication

Time management

Analytical skills

Formazione

Life Science Degrees

Descrizione del lavoro

A leading global pharmaceutical company is looking for a Regulatory Affairs Manager to develop strategies and manage regulatory submissions for Emerging Markets. The ideal candidate will have 3 to 5 years of experience in regulatory affairs, a Life Science degree, and strong communication skills. This role offers a challenging environment where you will work both independently and as part of a team.