Regulatory Nonclinical Writer - Clear, Precise Submissions

R&D Partners; Welwyn Garden City; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading life sciences recruiter is seeking a Non-Clinical Scientific Writer to manage submissions of nonclinical documents to regulatory agencies. The ideal candidate will have a university degree in a life science discipline and several years of experience in scientific writing. This role requires strong attention to detail, excellent communication skills, and a proactive approach to problem-solving. Join a dedicated team focused on high-quality document production and regulatory compliance in a dynamic environment in Welwyn Garden City.

Qualifications

• Several years of experience in scientific writing and editing within a nonclinical regulatory domain.
• Proficiency in writing and editing tools with a willingness to explore new technologies.

Responsibilities

• Manage the preparation and submission of nonclinical summary documents for regulatory applications.
• Collaborate with regulatory and scientific teams to ensure accurate nonclinical dossiers.
• Work with project leaders and scientists to compose regulatory submission documents.

Skills

Scientific writing

Editing

Interpersonal communication

Detail-oriented

Problem-solving

Education

University degree in a life science discipline

Tools

Writing and editing software

Job description

A leading life sciences recruiter is seeking a Non-Clinical Scientific Writer to manage submissions of nonclinical documents to regulatory agencies. The ideal candidate will have a university degree in a life science discipline and several years of experience in scientific writing. This role requires strong attention to detail, excellent communication skills, and a proactive approach to problem-solving. Join a dedicated team focused on high-quality document production and regulatory compliance in a dynamic environment in Welwyn Garden City.