Eu&Int Regulatory Affair Manager

Iqvia Italia; Ancona; In loco; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading global pharmaceutical company is seeking an EU & INT Regulatory Affair Manager in Ancona, Italy. The candidate will develop regulatory strategies for Emerging Markets, manage regulatory submissions, and provide guidance on compliance and documentation. Ideal candidates should have 3-5 years of regulatory affairs experience and a Life Science degree. This role offers a supportive environment with opportunities for professional growth.

Competenze

• 3 to 5 years of experience in corporate regulatory affairs roles.
• In-depth knowledge in drug development.
• Ability to manage complex assignments.

Mansioni

• Develop regulatory strategies for Emerging Markets.
• Plan and manage regulatory submissions to regional agencies.
• Provide regulatory guidance to colleagues from other functional areas.

Conoscenze

Regulatory Affairs

Drug Development Knowledge

Written and Oral Communication

Time Management

Problem-Solving

Leadership

Formazione

Life Science Degrees

Descrizione del lavoro

On behalf of our Client - Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry a global pharmaceutical company - IQVIA is looking for a EU & INT Regulatory Affair Manager who can join an exciting working environment in a dynamic atmosphere.

RESPONSIBILITIES

• Develop regulatory strategies for the Emerging Markets countries to meet Chiesi Global Rare Diseases Regulatory Affairs relevant objectives, with regional Head limited supervision
• In collaboration with consultants, partners and affiliates, plan, coordinate and manage regulatory submissions to regional agencies throughout the life cycle of GRD products
• In full alignment with the regional Head, provide advice and guidance regarding regional regulatory requirements driving the development and geographical expansion of GRD products.
• Contribute to the preparation and / or review of submissions to relevant markets to ensure the high quality of the documentation
• In agreement with the regional Head, communicate directly with regional regulatory authorities on behalf of Chiesi GRD to negotiate strategies and actions associated with regulatory submissions
• Critically review regulatory submission documents, periodic updates, overviews, summaries, etc., make recommendations for improvement and ensure adequacy for submission.
• Contributes to the development of processes and the preparation of Standard Operating Documents for GRD Regulatory Affairs
• In full alignment with the regional Head, provide regulatory guidance to colleagues from other functional areas
• Provide regulatory expertise in support of due diligence assessments
• Represent the Regulatory Department at the Core Team as a global RA member, where needed
• Support the Regional GRD Regulatory Affairs Head in the preparation of the needed documents for the meetings and interactions with regional regulatory authorities

REQUIREMENTS AND SKILLS

• Experience required: 3 to 5 years of experience in corporate regulatory affairs roles with an in-depth knowledge in the drug development
• Education: Life Science Degrees
• Technical Skills: good level
• Soft Skills:
• flexible, collaborative, open minded
• Well-developed written and oral communication and listening skills
• Well-developed time management skills and demonstrated ability to manage complex assignments.
• Experience in leadership and coaching is an asset.
• Well-developed analytical and problem-solving skills.
• Ability to work independently and as part of a team.

TYPE OF CONTRACT

Chemical Contract

IQVIA reserves the right to evaluate candidates with domicile / residence and work experience / study with requirements responding to the open request. Applications WITHOUT the requirements Will NOT be fully taken into