Senior Medical Writer – Regulatory Writing

This is a fully remote position, open to applicants in North Carolina.

📋 Description

• Act as the lead author for the creation of standard documents such as clinical study reports.

• Conduct research and refine intricate clinical and scientific documents.

• Evaluate standard documents produced by junior team members.

• Ensure adherence to quality processes and standards.

⛳️ Requirements

• A Bachelor's degree in a scientific field or equivalent experience.

• A minimum of 5 years of prior experience in the pharmaceutical or CRO industry is preferred.

• Additional credentials in medical writing (AMWA; EMWA; RAC) are beneficial.

• Exceptional skills in data interpretation and medical writing.

• Strong abilities in project management.

• Proficient computer skills and familiarity with client templates.

🏝️ Benefits

• Support for health and wellbeing.

• Opportunities for professional development.