Senior Translational Science Writer for Submissions

Net2Source (N2S); Madison (NJ); Hybrid; USD 82,656 - 93,635; Full time

Job summary

A leading pharmaceutical consultancy in Madison, NJ, seeks a Scientific Writer for Translational Development. The role involves writing regulatory documents, collaborating with scientists, and ensuring timely publication of outputs. Requires a Masters or PhD in relevant fields and extensive experience in scientific writing and drug development. This position offers a hybrid work model and a competitive pay rate, with extensive interaction with global teams and regulatory agencies.

Qualifications

• 8-10 years of scientific or regulatory writing experience.
• 5+ years of experience in drug development/pharmaceutical industry.
• Experience with publishing regulatory documents.

Responsibilities

• Write scientific documents including biomarker reports and regulatory submissions.
• Collaborate with TD scientists to establish publication goals.
• Ensure timely delivery for the TD writing book of work.

Skills

Scientific writing

Regulatory submissions

Communication strategy development

Clinical data analysis

Project management

Education

Masters or PhD in molecular biology, oncology, or related field

Tools

CARA

VERITY

Job description

A leading pharmaceutical consultancy in Madison, NJ, seeks a Scientific Writer for Translational Development. The role involves writing regulatory documents, collaborating with scientists, and ensuring timely publication of outputs. Requires a Masters or PhD in relevant fields and extensive experience in scientific writing and drug development. This position offers a hybrid work model and a competitive pay rate, with extensive interaction with global teams and regulatory agencies.