Sponsor Dedicated Protocol Medical Writer II

The role

You'll partner closely with Clinical Scientists to lead the clear and accurate completion of medical writing deliverables, focusing on clinical study protocols and protocol amendments. Working within a sponsor-dedicated team, you'll coordinate medical writing activities across departments, resolve client comments, and complete documents such as clinical study reports, patient narratives, investigator brochures, and regulatory submissions. You'll also mentor less experienced medical writers, act as a peer reviewer, and ensure adherence to FDA, ICH, and AMA standards. This is a remote full-time role open to candidates based in Portugal, the UK, or Canada, with minimal travel required (less than 25%).

Tools and skills