Preclinical Scientific Writer II/III — GLP Docs Pro

Pharmaron Beijing Co. Ltd.; Carlsbad (CA); On-site; USD 70,000 - 85,000; Full time

Benefits offered by this job

Medical Insurance

401(k) Plan

Paid Time Off

HSA contributions

Life Insurance

Wellness programs

Job summary

Pharmaron Beijing Co. Ltd. seeks a Scientific Writer II/III for Preclinical Research in Carlsbad, CA, on-site. You will craft nonclinical study protocols, reports, and regulatory documents supporting pharmaceutical and medical device research.

Ideal candidates translate complex preclinical data into precise, GLP-compliant documentation, collaborating with study directors and cross-functional teams in a fast-paced CRO setting.

Qualifications

• Bachelor's, Master's, or Ph.D. degree in Life Sciences or related field.
• Experience writing nonclinical study protocols, reports, or regulatory documents in CRO/pharma environments.
• Strong ability to translate complex preclinical data into clear, regulatory-compliant documents.

Responsibilities

• Develop and finalize nonclinical study protocols, reports, and scientific documents.
• Translate complex preclinical data into clear, accurate protocols and reports.
• Create publication-quality tables, figures, and data visuals communicating study results.

Skills

Scientific writing

Preclinical research

Regulatory documentation

GLP knowledge

Education

Bachelor's/Master's/PhD in Life Sciences

Tools

Provantis

Job description

Pharmaron Beijing Co. Ltd. seeks a Scientific Writer II/III for Preclinical Research in Carlsbad, CA, on-site. You will craft nonclinical study protocols, reports, and regulatory documents supporting pharmaceutical and medical device research.

Ideal candidates translate complex preclinical data into precise, GLP-compliant documentation, collaborating with study directors and cross-functional teams in a fast-paced CRO setting.