Principal Medical Writer

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Direct the creation of high-quality regulatory and clinical documents.

• Manage medical writing workstreams, ensuring that deliverables align with quality and timeline standards.

• Draft and review clinical study reports, protocols, and regulatory documents for precision and clarity.

• Collaborate with cross-functional teams to collect and integrate information for document creation.

• Offer insights on medical writing best practices and ensure compliance with regulatory standards.

• Mentor and train junior medical writers, promoting a culture of excellence and professional development.

• Keep abreast of industry trends and regulatory guidelines.

⛳️ Requirements

• A bachelor's degree in life sciences, pharmacy, or a related field.

• Extensive experience in medical writing, especially in regulatory submissions and clinical documentation.

• Experience in Neuroscience is highly advantageous.

• Strong grasp of regulatory requirements and industry standards for clinical writing.

• Outstanding writing and editing abilities, with a sharp focus on detail and clarity.

• Excellent communication and interpersonal skills, facilitating effective collaboration with diverse teams and stakeholders.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.