Medical Writer

Roles & Responsibilities
• Author and review regulatory medical writing documents including Clinical Study Reports (CSRs), protocols, Investigator’s Brochures (IBs), Informed Consent Forms (ICFs), and submission documents
• Act as lead writer or submission coordinator for assigned projects
• Manage and coordinate contributions from multiple writers across related deliverables
• Serve as the primary point of contact for clients, ensuring clear communication and timely delivery
• Drive process improvements and contribute to development of medical writing best practices
• Mentor, train, and technically guide junior medical writers
• Support business development activities by contributing to proposals and client interactions

Qualification
• Bachelor’s or advanced degree in Life Sciences, Healthcare, Pharmacy, or related discipline

Experience
• Minimum 6+ years of experience in regulatory medical writing
• Proven expertise in authoring key clinical and regulatory documents
• Experience across multiple therapeutic areas including vaccines, immunology, oncology, cardiovascular, neurology, infectious diseases, endocrine, gastrointestinal, autoimmune, and mental health

Skills
• Strong scientific, analytical, and regulatory writing skills
• Excellent communication and stakeholder management abilities
• Ability to lead projects independently and manage multiple timelines
• High attention to detail with strong quality and compliance focus
• Capability to work under pressure and manage variable workloads

About the Company
VUEVERSE is a specialized medical communications and regulatory writing organization delivering high-quality, compliant scientific and regulatory content to pharmaceutical and CRO clients across global markets, with a strong focus on expertise, innovation, and mentorship.