Scientific Writer

Ladders; United States; Remote; USD 110.000 - 179.000; Vollzeit

Benefits dieser Stelle

Impactful work

Growth opportunities

Collaborative teams

Science-driven culture

Zusammenfassung

Ladders is seeking a Scientific Writer to develop clear, scientifically rigorous content supporting nonclinical drug development and regulatory submissions. You will synthesize pharmacology, PK, and PD data into narratives that advance programs through milestones, working with scientists and cross-functional teams.

The role emphasizes timely delivery, accurate messaging, and consistent documentation across programs, with a remote-US based work arrangement and strong growth opportunities in a

Qualifikationen

• Bachelor's degree in life sciences; advanced degree (MS or PhD) preferred.
• Experience in scientific and regulatory writing for nonclinical development.
• Familiarity with pharmacology, PK, and PD data.
• Knowledge of drug development and eCTD guidelines.
• Proficiency in document authoring and collaboration tools in regulated settings.

Aufgaben

• Independently author nonclinical PK/PD study reports and eCTD summaries.
• Lead development of integrated regulatory narratives synthesizing PK, PD, and mechanistic data.
• Collaborate with scientists to ensure consistent PK/PD messaging.
• Coordinate data inputs, reviews, and stakeholder communications for timely deliverables.
• Drive process improvements through authoring guidance and workflow optimization.
• Serve as the scientific writing lead for assigned programs.

Kenntnisse

Scientific writing

Regulatory writing

Pharmacology

PK/PD data understanding

Regulated document drafting

Ausbildung

Bachelor's degree in life sciences

MS or PhD preferred

Jobbeschreibung

For our client, we are seeking a Scientific Writer to join the team of a leader in the Pharmaceuticals & Biotech space.

This role will focus on developing clear, scientifically rigorous content that supports nonclinical drug development and regulatory submissions. You will synthesize complex pharmacology, PK, and PD data into narratives that help advance programs through key development milestones. The position partners closely with scientists and cross-functional stakeholders to ensure accurate messaging, timely delivery, and consistent documentation across assigned programs.

Location: Remote - US based candidates only, no visa sponsorship available

Compensation: $109,900 - $179,300 annually

Responsibilities

• Independently author nonclinical PK/PD study reports and eCTD summaries
• Lead development of integrated regulatory narratives synthesizing PK, PD, and mechanistic data
• Collaborate with scientists to ensure consistent PK/PD messaging
• Coordinate data inputs, reviews, and stakeholder communications for timely deliverables
• Drive process improvements through authoring guidance and workflow optimization
• Serve as the scientific writing lead for assigned programs

Qualifications

• Bachelor's degree in life sciences; advanced degree (MS or PhD) preferred
• Experience in scientific and regulatory writing for nonclinical development
• Familiarity with pharmacology, PK, and PD data
• Knowledge of drug development and eCTD guidelines
• Proficiency in document authoring and collaboration tools in regulated settings

Benefits

• Opportunity to contribute to impactful drug development
• Work in a fast-growing, science-driven organization
• Collaborative environment with cross-functional teams
• Potential for professional growth and development

Our client is an equal opportunity employer. We encourage you to apply even if you don’t meet every qualification—your background could be exactly what this team needs.