
51 - 200 employees
Founded 2019
🧬 Biotechnology
💊 Pharmaceuticals
🤖 Artificial Intelligence
💰 Series B on 2024-04
Biotechnology • Pharmaceuticals • Artificial Intelligence
Iambic Therapeutics is a pioneering biotechnology company that leverages advanced AI algorithms for drug discovery. Their innovative, high-throughput experimental platform aims to address unmet patient needs by optimizing molecules for various therapeutic targets. The company's AI-driven approach allows it to rapidly explore chemical spaces, revealing novel drug mechanisms and delivering high-quality leads at an accelerated pace compared to traditional methods.
🕒 May 21
Improve your chances of getting an interview by checking your resume score before you apply.

51 - 200 employees
Founded 2019
🧬 Biotechnology
💊 Pharmaceuticals
🤖 Artificial Intelligence
💰 Series B on 2024-04
Biotechnology • Pharmaceuticals • Artificial Intelligence
Iambic Therapeutics is a pioneering biotechnology company that leverages advanced AI algorithms for drug discovery. Their innovative, high-throughput experimental platform aims to address unmet patient needs by optimizing molecules for various therapeutic targets. The company's AI-driven approach allows it to rapidly explore chemical spaces, revealing novel drug mechanisms and delivering high-quality leads at an accelerated pace compared to traditional methods.
• Lead the planning, authoring, and delivery of key development documents (INDs, protocols, IBs, CSRs, Health Authority responses, briefing documents, etc) • Provide strategic input on document content, messaging, and regulatory expectations • Partner cross-functionally with Clinical, Nonclinical, Medical, Biostats, CMC, and Regulatory teams • Establish and refine medical writing processes, templates, and standards • Implement and manage efficient document workflows and timelines • Support development of abstracts, posters, and presentations for scientific conferences • Evaluate and integrate AI tools to enhance writing quality and efficiency • Manage external vendors and contribute to building internal capabilities over time • Ensure consistency, quality, and accuracy across all deliverables • Advise cross-functional leadership on regulatory communication strategy and global document planning
• Bachelor’s degree required; advanced degree (PhD, PharmD, MD) preferred • 15+ years of experience in biotech/pharma, with 10+ years in medical writing, prior experience in smaller or growing biotech environments preferred • Strong experience supporting IND submissions and clinical-stage programs • Strong scientific writing and editing skills, with attention to detail • Solid understanding of FDA/EMA regulations and ICH guidelines • Ability to lead cross-functional document development in a lean environment • Comfortable balancing strategic input with hands-on execution • Interest in applying AI tools to improve medical writing workflows
• company paid healthcare • flexible spending accounts • voluntary life insurance • 401K matching • uncapped vacation
Apply Now🕒 May 15
Technical Writer-Editor in a remote role supporting federal law enforcement operations. Delivering clear documentation for border security technology and agency communications.
🕒 April 13
Manager of Medical Writing overseeing clinical and regulatory document creation for Danaher Diagnostics. Leading a team while ensuring compliance with FDA and EU standards.
🇺🇸 United States – Remote
💵 $130k - $160k / year
⏰ Full Time
🟠 Senior
🔴 Lead
✏️ Content Writer
🦅 H1B Visa Sponsor
🕒 April 9
Staff Enterprise Proposal Writer transforming technical details into persuasive narratives at IonQ. Collaborating with cross-functional teams to enhance proposal quality and drive revenue growth.
🇺🇸 United States – Remote
💵 $97.1k - $126.7k / year
⏰ Full Time
🔴 Lead
✏️ Content Writer
🦅 H1B Visa Sponsor
🕒 April 6
Service Desk Lead managing operations for Army Contract Writing System with focus on team leadership and stakeholder collaboration. Ensuring efficiency and service level agreements in a remote capacity.
🇺🇸 United States – Remote
💵 $115k - $160k / year
⏰ Full Time
🟠 Senior
🔴 Lead
✏️ Content Writer
🦅 H1B Visa Sponsor
🕒 March 27
Director of Medical Writing to oversee medical writers and author content for regulatory submissions. Experience in pharma or biotech medical writing is essential.
🇺🇸 United States – Remote
💵 $212k - $291.5k / year
⏰ Full Time
🔴 Lead
✏️ Content Writer
🦅 H1B Visa Sponsor