Senior Medical Writer: Clinical & Regulatory Docs

ThermoFisher Scientific; México; Remote; MXN 600,000 - 850,000; Full time

Job summary

Thermo Fisher Scientific in Mexico seeks a Medical Writer to deliver high-quality medical and scientific writing from planning to final drafts. You will collaborate with internal and external clients to ensure clear, compliant communications.

You will author routine documents such as clinical study reports and study protocols, and assist with IBs, INDs, and MAAs when needed. Strong writing, data interpretation, and teamwork are essential.

Qualifications

• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification.
• 2+ years of experience or equivalent.
• Experience in pharmaceutical/CRO industry preferred.
• Experience in scientific writing advantageous.

Responsibilities

• Serve as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies.
• May assist with more complex clinical and scientific and program level documents, including IBs, INDs, and MAAs.
• Ensure compliance with quality processes and requirements for assigned documents. May assist in determining best practices, methods and techniques for achieving optimal results.
• May assist in program management activities. Duties could include assisting with developing timelines, budgets, and forecasts for assigned deliverables.
• Represent the department at project launch meetings, review meetings, and project team meetings.

Skills

Medical writing

Data interpretation

Editorial proofreading

Regulatory documentation

Team collaboration

Attention to detail

Communication skills

Education

Bachelor's degree in a scientific discipline

Tools

Excel

Outlook

Document management systems

Job description

Thermo Fisher Scientific in Mexico seeks a Medical Writer to deliver high-quality medical and scientific writing from planning to final drafts. You will collaborate with internal and external clients to ensure clear, compliant communications.

You will author routine documents such as clinical study reports and study protocols, and assist with IBs, INDs, and MAAs when needed. Strong writing, data interpretation, and teamwork are essential.