Senior Global Medical Writing Lead - Regulatory, Remote UK

Cpl Life Sciences; England; Hybrid; GBP 56,000 - 75,000; Full time

Job summary

A specialty pharmaceutical company is looking for a Senior Manager in Regulatory Medical Writing to lead projects and ensure the creation of high-quality regulatory documents. The role requires extensive experience in regulatory writing within the pharmaceutical industry and excellent communication skills. This position offers remote work with quarterly travel to the office in Surrey, UK, with a salary ranging from £56,000 to £75,000 plus bonuses.

Benefits

Car allowance

Bonus

Qualifications

• 10+ years relevant experience in pharmaceutical industry.
• Experience managing regulated documents in the pharmaceutical industry.
• Strong technical expertise in medical writing documents.

Responsibilities

• Acts as a primary lead for all assigned programs.
• Provides intellectual leadership to the global project team.
• Reviews documents ensuring they meet regulatory requirements.
• Participates in departmental project activities.

Skills

Leadership skills

Regulatory medical writing

Strong communication skills

Strategic thinking

Education

BA/BS degree or equivalent

PhD/Pharm D or MS/MA/MPH (preferred)

Job description

A specialty pharmaceutical company is looking for a Senior Manager in Regulatory Medical Writing to lead projects and ensure the creation of high-quality regulatory documents. The role requires extensive experience in regulatory writing within the pharmaceutical industry and excellent communication skills. This position offers remote work with quarterly travel to the office in Surrey, UK, with a salary ranging from £56,000 to £75,000 plus bonuses.