Copywriter Regulatory Portuguese - Italian

Es52; Madrid; Presencial; EUR 35.000 - 55.000; Jornada completa

Descripción de la vacante

A leading company in healthcare data science seeks an analytical professional to join their Madrid office. The role involves assessing regulatory information, monitoring changes, and enhancing intelligence processes. Ideal candidates will possess strong editing skills in multiple languages, be proficient in English, and have a good understanding of drug development processes.

Formación

• Proficiency in proofreading and editing in Portuguese, Italian, and Hungarian.
• Proficient in English and in navigating intelligence databases.

Responsabilidades

• Monitor agency websites and local press for regulatory updates.
• Communicate with stakeholders on updates impacting clinical trials.
• Develop regulatory intelligence processes to enhance efficiency.

Conocimientos

Proofreading

Editing

Research

Analytical Skills

Communication

Organizational Skills

Team Collaboration

Descripción del empleo

We are recruiting an enthusiastic new team member to join us at our Madrid Center of Excellence office!

This position will support monitoring and analyzing changes in the local regulatory environment, including guidance and regulations from authorities, trade organizations, working groups, and industry thought leaders, for both drug and medical devices activities and requests.

Responsibilities :

• Assess regulatory intelligence information for relevance and impact on industry processes, drug development projects, and regulatory strategies to enhance IQVIA's proprietary documents.
• Monitor agency and professional websites, local press, conferences, and select documents aligned with IQVIA's scope, editorial, and intelligence management processes.
• Identify critical business aspects and communicate effectively with internal and external stakeholders, providing regular updates on information impacting clinical trials, pharmacovigilance, manufacturing, quality, and other ad hoc requests.
• Synthesize information from regulatory documents and interactions with local experts as needed.
• Input data into systems or tools to support effective knowledge management of country-level operational intelligence data.
• Develop and improve regulatory intelligence processes and procedures to increase efficiency.

Required Knowledge, Skills, and Abilities :

• Proficiency in proofreading and editing in Portuguese, Italian, and Hungarian.
• Proficient in English.
• Ability to work remotely with international peers.
• Good understanding of drug development and commercialization processes.
• Research, analyze, and interpret critical regulatory information.
• Highly organized and able to work independently to meet deadlines.
• Team-oriented with strong relationship-building skills and ability to collaborate effectively.
• Attentive to detail and committed to quality output.
• Effective written and oral communication skills in a multidisciplinary team environment.
• Proficient in navigating intelligence databases.

Join IQVIA

Recognized as a great place to work in Spain, on Fortune's list of World's Most Admired Companies, and other industry awards. IQVIA is an equal opportunity employer, making decisions based on qualifications and merit, prohibiting discrimination based on age, race, gender, or other protected statuses.

At IQVIA, we push the boundaries of human and data science to make a significant impact, helping our customers create a healthier world. Our 70,000 employees worldwide apply their insight, curiosity, and courage every step of the way. Learn more at our website.

Key Skills : Presentation Skills, Marketing, Proofreading, Copy Editing, Adobe Creative Suite, Multichannel Marketing, SEO, Dispute Resolution, Copywriting, Creative Writing, Branding, Writing Skills

Employment Type : Full-Time

Experience : [Specify years]

Vacancy : 1