Compiles, writes, edits, and coordinates medical writing deliverables that present scientific information clearly and accurately, and works as a medical writer within and across departments with moderate supervision.
Adheres to established regulatory standards, including ICH E3 guidelines, company standard operating procedures, client standards, company and/or client-approved templates, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget.
Coordinates quality and editorial reviews. Leads document reviews, reviews documents as needed, and resolves comments from client.
Reviews statistical analysis plans and table/figure/listing specifications for appropriate content and for grammar, format, and consistency.
Interacts and builds good working relationships with clients, department head, and peers, as necessary, to produce writing deliverables.
Performs online clinical literature searches and complies with copyright requirements.




Continues professional development to grow awareness of industry standards and best practices to improve ability to meet client expectations.
Aware of budget specifications for assigned projects, working within the budgeted hours and communicating status and changes to medical writing leadership.
Summary Medical writer on clinical study or regulatory project teams. Writes, edits, and coordinates content for clinical/regulatory documents to ensure high-quality completion of all assigned writing projects.
Further, nothing contained herein should be construed to create an employment contract. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

📌 Medical Writer (España)
🏢 Syneos Health
📍 España