As the Director of Clinical Regulatory Writing, you'll be at the forefront of driving strategic communication excellence to achieve successful submissions and approvals
Job Summary
As the Director of Clinical Regulatory Writing, you'll be at the forefront of driving strategic communication excellence to achieve successful submissions and approvals.
Your role will involve developing communication strategies, optimize document delivery, and supporting talent growth within CVRM across all phases of clinical development.
You’ll influence pivotal regulatory outcomes for programs that address some of the world’s most prevalent diseases.
Matching Summary
As the Director of Clinical Regulatory Writing, you'll be at the forefront of driving strategic communication excellence to achieve successful submissions and approvals.
Skills & Requirements
Must-have
Clinical regulatory writing leadership
Cardiovascular Renal Metabolism portfolio
Drug development communications strategy
Lead submission activities and author documents
Influence stakeholders at highest levels
Develop and embed innovative best practices
Nice-to-have
AI tools for medical writing
Coaching and mentoring talent growth
Cross-functional team collaboration
Scientific excellence and patient impact
Key Requirements
Bachelor's degree in Life Sciences or related discipline
Significant experience in medical/regulatory writing
Proven ability to lead complex communication programs