Medical Writer (English Native) – Remote

Über das Unternehmen

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to pushing the boundaries of human science and data science to make the biggest impact possible for our customers and patients globally. Our diverse teams work across a broad range of therapeutic areas, delivering innovative solutions that accelerate healthcare breakthroughs.

Stellenbeschreibung

As a Medical Writer (English Native) at IQVIA, you will play a crucial role in developing high-quality, scientifically accurate, and regulatory-compliant medical and scientific documents. This is a remote position, allowing you to contribute your expertise from anywhere. You will be responsible for creating a variety of documents, including clinical study reports, protocols, investigator brochures, regulatory submissions, abstracts, manuscripts, and other medical communications. Your work will directly support the advancement of new therapies and medical insights, ensuring clear and compelling communication of complex scientific information to diverse audiences. We are looking for a detail-oriented professional with exceptional English writing skills and a strong understanding of medical science.

Hauptverantwortlichkeiten

• Authoring, editing, and reviewing a wide range of medical and scientific documents, including but not limited to clinical study reports, protocols, investigator brochures, regulatory submission documents, abstracts, and manuscripts.
• Ensuring all documents adhere to relevant regulatory guidelines (e.g., ICH GCP), company standard operating procedures (SOPs), and client specifications.
• Collaborating effectively with cross-functional teams, including clinical, biostatistics, regulatory, and pharmacovigilance departments, to ensure accuracy and consistency of data and messages.
• Interpreting and summarizing complex scientific and clinical data clearly and concisely.
• Managing multiple projects simultaneously, prioritizing tasks, and meeting deadlines in a fast-paced environment.
• Participating in internal and external meetings to discuss document content and strategy.
• Maintaining up-to-date knowledge of industry trends, regulatory requirements, and therapeutic areas.

Erforderliche Fähigkeiten

• Native English speaker with exceptional written and verbal communication skills.
• Minimum of 2 years of experience in medical writing within a CRO, pharmaceutical company, or biotech setting.
• Bachelor's degree in a life science, medical, or related field.
• Demonstrated ability to write clear, concise, and accurate scientific and medical documents.
• Strong understanding of clinical research, drug development processes, and regulatory guidelines (e.g., ICH GCP).
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Excellent attention to detail and organizational skills.
• Ability to work independently and as part of a remote team.

Bevorzugte Qualifikationen

• Advanced degree (Master's, PhD, PharmD, MD) in a relevant scientific or medical discipline.
• Experience with specific therapeutic areas such as Oncology, Cardiovascular, CNS, or Rare Diseases.
• Familiarity with medical writing software and reference management tools.
• Certification from a recognized medical writing association (e.g., EMWA, AMWA).

Vorteile & Zusatzleistungen

• Competitive salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance.
• Generous paid time off and holidays.
• Opportunities for professional development and continuous learning.
• Flexible 100% remote work environment.
• Access to a global network of experts and cutting-edge resources.
• Employee assistance programs and wellness initiatives.

Jetzt bewerben