FSP Principal Medical Writer (Regulatory) - Client-Dedicated

Embrace the opportunity to become a Principal Medical Writer (Regulatory) and lead the development of high-quality clinical and regulatory documents for global clients. Mentor junior writers, drive process improvements, and ensure compliance with industry standards. Shape the future of medical writing in a collaborative, innovative environment at Thermo Fisher Scientific.

Skills

• medical writing
• regulatory submissions
• clinical study report writing
• protocol development
• data interpretation
• document review
• project management
• training and mentorship
• stakeholder management
• presentation skills
• negotiation skills
• quality compliance
• performance metrics management
• therapeutic area knowledge
• neuroscience