Senior Medical Writer

This is a fully remote position, open to applicants in United States, +7 more locations.

📋 Description

• Independently strategize and create regulatory documents and medical communications that support all stages of product development.

• Organize, analyze, interpret, and present scientific and statistical data effectively.

• Ensure that all documents adhere to ICH, other regulatory guidelines, and the company’s document standards.

• Operate under the guidance of Medical Writing management.

• Collaborate with both internal and external teams involved in document production across various functions.

⛳️ Requirements

• A Bachelor’s degree is required, preferably in a science-related field.

• At least 5 years of medical writing experience within a contract research organization or in a pharmaceutical/biotechnology research environment.

• Other professional and/or educational experiences may be considered to meet this minimum requirement on a case-by-case basis.

• A minimum of 3 years of formal medical writing experience is essential.

• Advanced knowledge of ICH and related regulatory guidelines is required.

• Exceptional written English skills with a strong attention to detail.

• Strong interpersonal and communication abilities are necessary.

• Proficiency in Microsoft Office Suite, particularly with advanced Microsoft Word skills.

🏝️ Benefits

• Fully remote work arrangement.

• Flexible and inclusive workplace culture.

• Commitment to equal opportunity and an inclusive environment.