🧬 Hiring Now: Pharmaceutical Consultant Writer | Remote | Part-Time Contract
📅 Start: June 30, 2025 | ⏳ Duration: 7 months
🕐 Hours: ~20 hrs/week | 💼 Work Style: Fully Remote
We’re looking for an experienced Pharmaceutical Consultant Writer to support a leading gene therapy company’s Translational Medicine team. This is a high-impact role for someone with deep regulatory writing expertise and a strong understanding of FDA/EMA standards.
Key Responsibilities:
Provide strategic medical writing support and ensure consistency with internal documentation style guides
Draft and review GLP-related reports, training modules, and regulatory-facing content
Interpret scientific data from internal experts and ensure documents are audit-ready
Perform literature reviews and synthesize complex data for regulatory use
Ideal Candidate:
Advanced degree in Life Sciences, Pharmacy, or related
Strong track record in regulatory or medical writing within pharma/biotech
Familiar with GLP practices, preclinical development, and global regulatory frameworks
Regulatory Affairs Certification or PMP is a plus
🗨️ If you’re open to new consulting opportunities—or know someone who is—feel free to DM me! kelly.law@intelliprogroup.com
To apply for this job please visit www.linkedin.com.
