Senior Medical Writing Lead — Regulatory Strategy

Jazz Pharmaceuticals; Princes Risborough; On-site; GBP 116,000 - 176,000; Full time

Job summary

A leading biopharmaceutical company in the UK is seeking an Associate Director, Medical Writing to prepare high-quality regulatory documents and manage cross-functional collaboration. The ideal candidate will have strong English language skills, extensive experience in medical writing, and a deep understanding of the clinical development process. This role involves working globally and may include management responsibilities. Join a company dedicated to innovating life-changing medicines.

Benefits

Discretionary annual cash bonus

Comprehensive benefits including medical, dental, and vision insurance

401k retirement savings plan

Flexible paid vacation

Qualifications

• 8+ years writing experience in the pharmaceutical industry, or 5+ years with an advanced degree.
• Experience with global submissions and regulatory documentation is essential.

Responsibilities

• Prepare high-quality medical writing deliverables.
• Work with cross-functional teams to ensure effective data communication.
• Manage writers on programs with multiple deliverables.

Skills

English language proficiency

Lean authoring expertise

MS Office skills

Clinical development process knowledge

Influencing and negotiating skills

Project management

Education

BA/BS in relevant field

Advanced degree preferred

Tools

MS Word

MS PowerPoint

MS Excel

Job description

A leading biopharmaceutical company in the UK is seeking an Associate Director, Medical Writing to prepare high-quality regulatory documents and manage cross-functional collaboration. The ideal candidate will have strong English language skills, extensive experience in medical writing, and a deep understanding of the clinical development process. This role involves working globally and may include management responsibilities. Join a company dedicated to innovating life-changing medicines.