Clinical Trial Medical Writer - Senior

Drive quality in clinical trial documentation as a Senior Medical Writer with Syneos, located in Toronto, ON. This role focuses on regulatory submissions and document accuracy for trial transparency.
In this senior position, you will execute high-quality, project-specific writing activities, including the marking and review of critical documents such as patient narratives and clinical summaries. You will ensure compliance with international regulations while performing quality control checks and providing mentorship to junior writers as needed throughout the project lifecycle.

Key Responsibilities:

• Oversee project-specific writing with high quality

• Review and edit clinical documents for regulatory compliance

• Create summary documents for clinical trial protocols

• Perform quality control using established checklists

• Analyze processes to assess documentation quality
Requirements:

• Proven experience in medical writing focused on regulatory affairs

• In-depth knowledge of clinical trial regulations

• Ability to instruct and mentor team members

• Adherence to client-specific and company processes

• Participation in training necessary for the role
Apply your medical writing expertise at Syneos to enhance clinical trial transparency in Toronto!
#J-18808-Ljbffr