Remote Nonclinical Writer for Regulatory Submissions

MMS; Charleston (SC); Remote; USD 70,000 - 90,000; Full time

Job summary

A leading CRO in Charleston, SC is seeking a Nonclinical Writer to develop and manage nonclinical documents. The ideal candidate will have 2+ years of regulatory writing experience along with strong analytical and communication skills. This full-time, remote role offers the opportunity to work in a collaborative and innovative team. Join us at a company recognized for its exceptional culture in the pharmaceutical industry.

Qualifications

• 2+ years of pharmaceutical regulatory nonclinical writing experience.
• Hands-on experience with clinical trial and pharmaceutical development preferred.
• Basic understanding of CROs and drug development process.

Responsibilities

• Develop, write, and manage nonclinical documents.
• Lead projects independently and ensure compliance with regulatory guidelines.
• Collaborate with cross-functional teams.

Skills

Strong writing and analytical skills

Excellent written/oral communication

Time and project management skills

Ability to negotiate and collaborate

Knowledge of GLP, ICH guidelines

Education

BS in pharmacology, toxicology, biology or chemistry

Tools

MS Office applications

Job description

A leading CRO in Charleston, SC is seeking a Nonclinical Writer to develop and manage nonclinical documents. The ideal candidate will have 2+ years of regulatory writing experience along with strong analytical and communication skills. This full-time, remote role offers the opportunity to work in a collaborative and innovative team. Join us at a company recognized for its exceptional culture in the pharmaceutical industry.