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Senior Regulatory Clinical Document Specialist

2 weeks ago

Adelaide, South Australia beBeeRegulatory Full time $90,000 - $120,000
Regulatory Medical Writer Role

We are seeking a seasoned regulatory medical writer to support the development of clinical documents. As a key member of our team, you will be responsible for creating high-quality documents, including investigator brochures, clinical study protocols, and clinical study reports.

About This Opportunity

This role offers a unique chance to work in the pharmaceutical and biotechnology industry, supporting drug development from inception to commercialization. You will have the opportunity to collaborate with cross-functional teams, drive document quality, and contribute to the growth of our organization.

Responsibilities
  • Develop, write, and edit clinical documents to ensure accuracy and compliance
  • Provide technical expertise and guidance to internal stakeholders and external clients
  • Mentor junior medical writers and maintain high standards of quality and productivity
Requirements
  • Bachelor's degree in a scientific or relevant field (e.g., life sciences, pharmacy, or healthcare)
  • At least 2 years of experience in medical writing, preferably with a focus on clinical trial documents
  • Minimum 3 years of experience in the biotech/pharma/clinical research industry, demonstrating a strong understanding of regulatory requirements and industry standards
  • Excellent writing skills, with experience in crafting clear, concise reports and peer-reviewed publications
Benefits and Growth Opportunities

This role offers a competitive compensation package, opportunities for professional growth and development, and a supportive work environment that fosters collaboration and innovation. If you are a motivated and detail-oriented medical writer looking to make a meaningful contribution to the pharmaceutical and biotechnology industry, we encourage you to apply for this exciting opportunity.