[Hiring] Senior Regulatory Writing Specialist @Med Communications International

Role Description

The Medical Writer - Senior Regulatory Writing Specialist is a professional responsible for the creation of regulatory materials for investigational and marketed products in alignment with regulatory and compliance practices. The individual will work directly with client teams to manage regulatory writing projects.

Qualifications

• Above average attention to detail, teamwork, and initiative.
• Ability to interact with other departments within the company and be proficient in written and verbal communication.
• Proficient in Microsoft Word, Excel, PowerPoint, and Outlook, and quickly able to learn new software.
• Ability to apply regulatory guidelines to content development.

Requirements

• Advanced degree in a scientific discipline (e.g., life sciences, pharmacy, medicine) or relevant work experience; or equivalent combination of education, training, and experience.
• More than 2 years (typically 3-5 years) of experience in scientific/medical/regulatory writing in the pharmaceutical domain. Mastery of 3 or more regulatory document types.
• Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.

Company Description