Senior Medical Writer - Remote Contract for Regulatory Docs

TALENT Software Services; California (MO); Remote; USD 96,432 - 110,208; Full time

Job summary

A consulting firm specializing in IT is looking for a Senior Medical Writer to manage the medical writing function. The role involves drafting clinical study protocols, regulatory documents, and managing review timelines within a collaborative team environment. Candidates should have a scientific degree and significant experience in medical writing, with advanced knowledge of drug development processes and regulatory requirements. This full-time position is primarily remote, with a competitive pay range of $70 - $80 per hour.

Qualifications

• Minimum 6 years as a medical writer in pharmaceutical industry or 10 years in a related field.
• Experience with INDs and regulatory submissions preferred.
• Ability to interpret complex clinical data and present it clearly.

Responsibilities

• Draft and edit clinical study protocols and reports.
• Manage timelines and facilitate document review processes.
• Represent Global Medical Writing in cross-functional team meetings.

Skills

Medical writing experience

Regulatory document knowledge

Attention to detail

Effective communication

Education

Bachelor's or higher degree in scientific field

Tools

Microsoft Word

Adobe Acrobat

Document management software

Job description

A consulting firm specializing in IT is looking for a Senior Medical Writer to manage the medical writing function. The role involves drafting clinical study protocols, regulatory documents, and managing review timelines within a collaborative team environment. Candidates should have a scientific degree and significant experience in medical writing, with advanced knowledge of drug development processes and regulatory requirements. This full-time position is primarily remote, with a competitive pay range of $70 - $80 per hour.