Hybrid Global Nonclinical Regulatory Writer

Undisclosed; England; Hybrid; GBP 50,000 - 80,000; Full time

Job summary

Our client, a global pharmaceutical company, is seeking a Nonclinical Scientific Writer in the Hertfordshire area. This hybrid role involves supporting global regulatory submissions and working closely with nonclinical and regulatory teams throughout the development lifecycle.

The ideal candidate will have a strong background in life sciences and significant experience in nonclinical regulatory documentation. If you're passionate about collaborating across functions and delivering high-quality work, we want to hear from you.

Qualifications

• Proven experience in nonclinical regulatory submissions.
• Ability to collaborate across teams for high-quality documentation.
• Background in life sciences is crucial.

Responsibilities

• Support global regulatory submissions with high-quality documentation.
• Collaborate closely with nonclinical and regulatory teams.
• Contribute throughout the full development lifecycle.

Skills

Experience in nonclinical regulatory documentation

Collaborative skills

Strong background in life sciences

Job description

Our client, a global pharmaceutical company, is seeking a Nonclinical Scientific Writer in the Hertfordshire area. This hybrid role involves supporting global regulatory submissions and working closely with nonclinical and regulatory teams throughout the development lifecycle.

The ideal candidate will have a strong background in life sciences and significant experience in nonclinical regulatory documentation. If you're passionate about collaborating across functions and delivering high-quality work, we want to hear from you.