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Medical Writer Ii

3+ years
Not Disclosed
10 Feb. 13, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Medical Writer II at ICON plc

Location: Home-based in New Zealand | Hybrid: Office/Remote
Job Type: Permanent, Full-time
Job ID: JR126645


About ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization (CRO). We are committed to advancing healthcare and clinical research, fostering an inclusive environment where innovation thrives. Join us in shaping the future of clinical development.


Role Overview

As a Medical Writer II at ICON, you will be an integral part of the team, contributing to the preparation of clinical trial documents, regulatory submissions, and scientific publications. This is a great opportunity for those looking to advance their career in medical writing while playing a pivotal role in the advancement of innovative treatments and therapies.


What You Will Be Doing:

  • Document Preparation: Collaborate with cross-functional teams to write and edit clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), patient narratives, and other regulatory documents, ensuring compliance with internal standards and regulatory guidelines.
  • Literature Reviews and Data Analysis: Conduct literature reviews and interpret clinical trial results to support the development of scientific manuscripts, abstracts, posters, and presentations for publication in peer-reviewed journals and scientific conferences.
  • Data Validation: Review and validate clinical data, ensuring consistency with study protocols, SOPs, and regulatory requirements.
  • Collaboration: Participate in project meetings, teleconferences, and client interactions to provide feedback on document content and ensure smooth project execution.
  • Knowledge Updates: Stay updated on emerging trends, scientific developments, and regulatory updates, applying this knowledge to enhance clinical research projects.

Your Profile:

  • Educational Qualification: Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related field.
  • Experience: Minimum of 3 years of experience in medical writing within the pharmaceutical, biotechnology, or CRO industry.
  • Skills:
    • Proficiency in scientific and medical terminology.
    • Excellent written and verbal communication skills.
    • Strong analytical and critical thinking skills for interpreting clinical data.
    • Familiarity with regulatory requirements and industry guidelines.
    • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
    • Experience with document management systems and statistical analysis tools (preferred).

What ICON Can Offer You:

  • Competitive Salary: Along with a competitive salary, ICON offers various benefits designed to support your well-being and work-life balance.
  • Health Insurance: A range of health insurance options for you and your family.
  • Retirement Planning: Competitive retirement offerings to help you plan for the future.
  • Employee Assistance: Global Employee Assistance Programme (LifeWorks) offering 24-hour support.
  • Additional Benefits: Childcare vouchers, bike purchase schemes, discounted gym memberships, and more.

At ICON, we pride ourselves on fostering diversity and inclusion, ensuring an environment where all employees can thrive.


Interested?
ICON encourages you to apply, even if you don’t meet every requirement. You may be the perfect fit for this role or others at ICON.


Apply Today
For more details on benefits, visit our careers site.

Equal Opportunity Employer
ICON is committed to a workplace free from discrimination and harassment, providing equal consideration to all applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.