🛠 Tech Stack

💼 About This Role

You'll draft and edit abstracts, posters, and manuscripts for a leading genetic testing company. Your work will support clinical research and regulatory submissions while adhering to GPP3 and ICMJE guidelines. You'll collaborate with cross-functional teams to drive publication planning and ensure compliance.

🎯 What You'll Do

• Draft and copyedit abstracts, posters, and manuscripts
• Support writing for validation documents, protocols, and regulatory submissions
• Collaborate on publication planning and manage writing projects
• Format documents per journal and congress guidelines

📋 Requirements

• Doctoral degree (PhD, PharmD, or MD) in life sciences
• 2+ years scientific writing experience with peer-reviewed publications
• Experience submitting abstracts and manuscripts to congresses and journals
• Understanding of ICMJE and GPP guidelines

✨ Nice to Have

• Experience with Adobe Creative Suite, Graphpad, or Endnote
• Familiarity with electronic literature search tools

🎁 Benefits & Perks

• 🏖️ Comprehensive medical, dental, vision
• 💰 Free genetic testing for employees and family
• 👶 Pregnancy and baby bonding leave
• 🏦 401k benefits
• 🚆 Commuter benefits

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter phone screen· 30 min
2. 2Technical writing assessment· 60 min
3. 3Hiring manager interview· 45 min
4. 4Team interview· 45 min
5. 5Offer· 30 min