Associate Medical Writer

About

Elevate clinical research as you step into the role of Associate Medical Writer dedicated to producing high-quality study documentation. Collaborate with a dynamic team while ensuring compliance with all regulatory standards.

Your role will entail generating essential documentation across various clinical trial phases, including protocols and CSRs, while ensuring adherence to ICH and GCP guidelines. Engage in literature reviews and work closely with cross-functional teams to guarantee the accuracy and integrity of study materials. Your ability to produce grammatically precise content will be critical in supporting the clinical research process.

Key Responsibilities

• Create high-quality clinical study documents
• Review and verify documents for regulatory compliance
• Synthesize literature for study-related content
• Collaborate on protocol sections and necessary changes
• Respond to feedback from sponsor inquiries

Requirements

• Bachelor’s degree in Medical Sciences or related field
• One year of medical writing experience preferred
• Strong understanding of clinical trials processes
• Excellent editorial and communication skills
• Self-motivated with the ability to work under pressure

Make your mark in clinical writing and contribute to innovative research efforts while ensuring strict compliance and high standards in documentation.