Scientific Writer (English) – Remote

Über das Unternehmen

Parexel is a leading global clinical research organization (CRO) dedicated to accelerating the development of innovative new therapies to improve worldwide health. With a strong commitment to quality and patient safety, we partner with pharmaceutical, biotech, and medical device companies to navigate complex regulatory landscapes and bring life-changing treatments to market faster. Our global team is comprised of diverse experts united by a shared passion for advancing medical science.

Stellenbeschreibung

We are seeking a highly motivated and detail-oriented Scientific Writer to join our global remote team. In this role, you will be responsible for developing high-quality, scientifically accurate, and compliant clinical and regulatory documents. This is a fantastic opportunity for an individual with a strong scientific background and excellent English writing skills to contribute to cutting-edge research and make a tangible impact on patient lives from anywhere in the world.

Hauptverantwortlichkeiten

• Prepare a variety of clinical and regulatory documents including study protocols, clinical study reports (CSRs), investigator brochures (IBs), and informed consent forms (ICFs).
• Ensure all documents adhere to company standards, client specifications, and relevant regulatory guidelines (e.g., ICH GCP, FDA, EMA).
• Collaborate effectively with cross-functional teams, including clinical, biostatistics, regulatory affairs, and project management, to gather necessary information and facilitate document review.
• Conduct thorough literature searches and synthesize complex scientific data clearly and concisely.
• Manage multiple projects simultaneously, meeting deadlines and maintaining high quality standards.
• Participate in client meetings and teleconferences as required.
• Maintain current knowledge of industry best practices and regulatory requirements for medical writing.

Erforderliche Fähigkeiten

• Native-level proficiency in English with exceptional writing, editing, and verbal communication skills.
• Ph.D. or Master's degree in a life science, medical, or related scientific discipline.
• Demonstrated ability to interpret and present complex scientific data accurately and clearly.
• Strong understanding of clinical research principles, drug development processes, and regulatory requirements (e.g., ICH GCP).
• Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint) and reference management software.
• Excellent attention to detail and commitment to quality.
• Ability to work independently and as part of a virtual team in a fast-paced environment.

Bevorzugte Qualifikationen

• Previous experience (at least 2 years) in medical writing within a CRO, pharmaceutical company, or biotech setting.
• Experience with specialized software for document management or statistical analysis.
• Familiarity with electronic document management systems (EDMS).
• Professional certification in medical writing (e.g., EMWA, AMWA).

Vorteile & Zusatzleistungen

• Competitive salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance.
• Flexible working hours and work-life balance initiatives.
• Generous paid time off and public holidays.
• Opportunities for professional development and career growth.
• Access to a global network of scientific experts.
• Home office stipend and ergonomic support for remote work.

Jetzt bewerben