Technical Writer

📋 Description

• Plan and start-up activities for new clinical studies
• Liaise to ensure study activities meet Work Order timelines
• Maintain records to applicable standards
• Prepare and review reports: assay validation, manuals, protocols
• Produce internal and client reports
• Adhere to ISO 17025, OECD GLP, NATA and ICH GCP

🎯 Requirements

• Bachelor of Science (Hons) or equivalent (Essential)
• PhD in Biological discipline (Desirable)
• Experience in medical laboratory techniques (Essential)
• Experience preparing technical documents (Desirable)
• Excellent organisational and writing skills (Essential)
• Proficient with Word, Excel, PowerPoint (Essential)

🎁 Benefits

• Development opportunities across local and global roles
• Work with leading technology in PK/PD assays
• Flexible, equal opportunity employer
• Wellbeing and connection initiatives for staff
• Collaborative, inclusive team culture
• Training and professional activities supported