Senior Medical Writing Project Manager

• Develop project timelines, standards, budgets, and forecasts
• Collaborate with cross-functional teams to meet deliverables
• Monitor timelines and provide status updates
• Identify and resolve client management issues
• Ensure compliance with quality processes
• Lead initiatives involving Informed Consent Forms (ICFs) and other critical clinical research documents
• Deliver high-quality, compliant documentation

• Prefer BS/BA in a scientific field with 5 years' experience, or an advanced degree with 3 years' experience
• Experience managing medical writing or clinical projects
• Pharmaceutical/CRO industry experience preferred
• Experience in regulatory and/or plain language medical writing advantageous
• Proven project management skills
• Strong planning and organizational abilities
• Excellent interpersonal and communication skills
• Ability to work independently and under pressure
• Solid project management, budgeting, and forecasting skills
• Effective problem-solving and decision-making abilities
• Proficient in global and regional regulatory guidelines

• Competitive remuneration
• Annual incentive plan bonus
• Healthcare
• Employee benefits
• Career and development prospects
• Innovative, forward-thinking company culture