Medical/Scientific Writer

This is a fully remote position, open to applicants in Armenia, +1 more country.

📋 Description

• Develop and manage medical communications materials, such as slide presentations, congress materials, manuscripts, abstracts, posters, and advisory board presentations.

• Prepare regulatory documents including clinical study reports, investigator brochures, and informed consent forms.

• Create publications for peer-reviewed journals in accordance with GPP3/ICMJE standards.

• Develop educational resources for healthcare professionals and patient-centric content.

• Oversee multiple projects concurrently while adhering to deadlines and maintaining quality standards.

• Facilitate cross-functional reviews involving medical, regulatory, and commercial teams.

• Monitor project timelines, budgets, and deliverables utilizing project management tools.

• Engage in client meetings and status update calls.

• Conduct literature reviews and extract data from clinical trial databases.

• Integrate data from clinical studies, meta-analyses, and systematic literature reviews.

• Ensure the accuracy and consistency of scientific content with source documents.

• Stay informed about therapeutic landscapes and competitive intelligence.

• Ensure compliance with FDA, EMA, and ICH-GCP guidelines in all content.

• Apply client style guides, brand guidelines, and standard operating procedures.

• Participate in quality control and peer review processes.

• Maintain document version control and archival practices.

• Build and nurture client relationships through effective and timely communication.

• Understand client requirements and offer strategic recommendations.

• Contribute to proposal development and scoping efforts.

• Assist in new business development activities.

⛳️ Requirements

• Advanced degree (PhD, PharmD, MD, MS) in life sciences, pharmacy, medicine, or a related discipline; a Bachelor's degree with exceptional experience may be considered.

• At least 4 years of medical writing experience within the pharmaceutical industry, CRO, or medical communications agency.

• Demonstrated success in delivering publications, regulatory documents, and congress materials.

• Exceptional medical writing capabilities.

• Proficiency in Microsoft Office.

• Familiarity with reference management software.

• Knowledge of clinical trial databases.

• Strong project management abilities.

• Excellent communication skills.

• Preferred: Experience with Veeva.

• Preferred: Therapeutic knowledge in oncology, immunology, or metabolic disorders.

• Preferred: Skills in creative design.

• Preferred: Understanding of HEOR.

• Preferred: Experience in mentoring teams.

🏝️ Benefits

• Competitive salary and performance-based bonuses.

• Comprehensive health, dental, and vision insurance.

• Opportunities for professional development and continuing education.

• Flexible work arrangements and a supportive work environment.

• Generous paid time off and holiday policies.