Therapeutic Area Specialist

4 days ago


Auckland, Auckland, New Zealand ICON Full time

We're seeking a talented Medical Writer II to join our team at ICON. With a focus on advancing innovative treatments and therapies, our organization is dedicated to shaping the future of clinical development.

Key Responsibilities

As a Medical Writer II at ICON, you'll be responsible for:

  1. Preparing, writing, and editing clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), patient narratives, and other regulatory documents in compliance with internal standards and regulatory guidelines.
  2. Conducting literature reviews, data analysis, and interpretation of clinical trial results to support the development of scientific manuscripts, abstracts, posters, and presentations for publication in peer-reviewed journals and scientific conferences.
  3. Reviewing and validating clinical data, ensuring accuracy, completeness, and consistency with study protocols, standard operating procedures (SOPs), and regulatory requirements.
  4. Participating in project meetings, teleconferences, and client interactions to discuss project objectives, timelines, and deliverables, while providing input and feedback on document content, format, and presentation.
  5. Staying up-to-date with emerging trends, scientific developments, and regulatory updates in relevant therapeutic areas, and applying medical writing principles and best practices to support successful clinical research projects.
Requirements

To succeed as a Medical Writer II at ICON, you'll need:

  • A Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related field, with a minimum of 3 years of experience in medical writing within the pharmaceutical, biotechnology, or contract research organization (CRO) industry.
  • Proficiency in scientific and medical terminology, with excellent written and verbal communication skills, attention to detail, and the ability to convey complex information in a clear and concise manner.
  • Strong analytical and critical thinking skills, with the ability to review and interpret clinical data, identify key findings and trends, and communicate results effectively to diverse stakeholders.
  • Familiarity with regulatory requirements, industry guidelines, and publication standards governing the preparation and submission of clinical trial documents and scientific manuscripts.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and familiarity with document management systems, reference management software, and statistical analysis tools preferred.
About ICON

ICON is a world-leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development. Our mission is to advance innovative treatments and therapies, and we're committed to fostering an inclusive environment that rewards high performance and nurtures talent.

We offer a competitive salary, a range of health insurance options, competitive retirement planning offerings, and flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.



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