Principal Regulatory Medical Writer - Oncology

Join Syneos Health as a Senior Principal Regulatory Medical Writer in Oncology in Toronto, ON, where your expertise will shape regulatory submissions globally. Manage comprehensive medical writing projects and collaborate closely with key stakeholders.
In this pivotal role, you'll develop regulatory documents in compliance with global standards and contribute to the success of medical writing initiatives. Your project management skills will ensure accurate timelines and effective communication within cross-functional teams. Engaging in collaborative meetings will further enhance the delivery of regulatory documents.

Key Responsibilities:

• Prepare regulatory documents adhering to global ICH guidelines

• Manage medical writing timelines for projects

• Collaborate in cross-functional discussions on deliverables

• Review related documents to ensure alignment

• Preferred:

Experience with eCTD submissions
Requirements:

• Significant background in regulatory medical writing

• Excellent communication and project management skills

• Understanding of ICH and regulatory processes

• Able to work in cross-functional group settings

• Preferred:

Experience with eCTD submissions
Bring your regulatory writing expertise and project management acumen to Syneos Health in Toronto and make a difference in oncology.
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