Regulatory Documentation Scientist (Remote/Hybrid)

Proclinical Group; England; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading regulatory consultancy firm in the United Kingdom is seeking a Regulatory Documentation Scientist to manage the preparation and submission of nonclinical regulatory documents. You will ensure high-quality documentation for regulatory submissions collaborating with cross-functional teams. This position offers flexibility with remote or hybrid work options, making it ideal for balancing productivity and collaboration. The candidate should possess a relevant degree and experience in scientific writing, along with strong collaboration skills.

Qualifications

• Experience in scientific writing and editing within a nonclinical regulatory domain.
• Proficiency with writing technologies and tools.
• Strong skills in collaboration and effective communication.

Responsibilities

• Manage the preparation and submission of nonclinical summary documents.
• Collaborate with teams for comprehensive nonclinical dossiers.
• Draft regulatory submission documents and study reports.
• Develop processes and guidelines for document production.
• Represent the nonclinical team in global regulatory initiatives.

Skills

Scientific writing

Collaboration

Communication skills

Problem-solving

Education

University degree in a life science discipline

Tools

Writing and editing software

Job description

A leading regulatory consultancy firm in the United Kingdom is seeking a Regulatory Documentation Scientist to manage the preparation and submission of nonclinical regulatory documents. You will ensure high-quality documentation for regulatory submissions collaborating with cross-functional teams. This position offers flexibility with remote or hybrid work options, making it ideal for balancing productivity and collaboration. The candidate should possess a relevant degree and experience in scientific writing, along with strong collaboration skills.