Elevate your career as a Senior Medical Writer with Amaris Consulting, focusing on regulatory content strategies in a hybrid work setting. Lead global submissions and ensure compliance through high-quality documentation.

Amaris

Consulting is seeking an experienced Senior Medical Writer to develop and execute regulatory strategies. You will manage clinical dossiers, review documents for compliance, and collaborate with cross-functional teams. This role demands solid expertise in regulatory processes and excellent communication skills to drive successful interactions with health authorities. Key Responsibilities:
Lead regulatory content strategies for global submissions
Manage preparation of clinical dossiers and safety documents




Review regulatory documents for accuracy and compliance
Collaborate with stakeholders for timely submission delivery
Mentor less experienced writers and contribute to continuous improvement Requirements:
Bachelor’s in Life Sciences or related field
Minimum 5 years regulatory writing experience
Robust knowledge of ICH, GCP, and other guidelines
Proficient in Google Workspace and Microsoft Office
Fluent in English both written and spoken Contribute your project management and regulatory writing expertise to enhance global submission efforts at Amaris Consulting.

📌 Senior Medical Writer For Regulatory Strategies Mississauga
🏢 MANTU GROUP
📍 Mississauga