Analytical Writer

Roles & Responsibilities:
• Prepare bioanalytical and method validation reports using laboratory and project data
• Translate complex scientific results into clear, structured narratives for regulatory and client review
• Collaborate with Project Managers, Bioanalytical Team Leads, and laboratory scientists
• Review documentation for accuracy, consistency, and regulatory compliance
• Finalize reports according to international guidelines and eCTD PDF standards
• Develop and maintain reporting templates and support study documentation

Qualification:
• Bachelor’s degree in Life Sciences, Biomedical Sciences, Pharmacy, or related discipline

Experience:
• 2–4 years in bioanalytical laboratory or clinical/non-clinical study environments
• Experience with techniques such as LC-MS/MS, HPLC, ELISA, ADA, NAb, and Flow Cytometry

Skills:
• Strong analytical and scientific writing skills
• Excellent English communication (written and verbal)
• Proficiency in MS Word, Excel, and Adobe tools
• Detail-oriented, well-organized, and able to manage multiple priorities

About the Organization:
ICON plc is a global leader in healthcare intelligence and clinical research, providing innovative solutions and regulatory-compliant support to pharmaceutical, biotechnology, and medical device clients worldwide.