Principal Medical Writing Lead

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🏄 California, Florida, +2 more states – Remote

🏄 California – Remote 🐊 Florida – Remote 🗽 New York – Remote 🍂 Massachusetts – Remote

💵 $140k - $200k / year

⏰ Full Time

🟠 Senior

✏️ Content Writer

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Faro Health Inc.

WebsiteLinkedInAll Job Openings

11 - 50 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $20M Series A on 2023-02

Healthcare • Consulting • Logistics

Faro Health Inc. is a company that specializes in streamlining and optimizing the development of clinical trial protocols using its AI-enabled software platform. The company's solutions are focused on enhancing the efficiency, consistency, and quality of clinical trials by providing tools for data-driven protocol design and seamless collaboration. Faro Health's platform also aims to reduce patient burden, trial risk, and costs, while increasing the speed of clinical research progress. Through their Study Designer tool and generative AI Co-Author, Faro Health enables research teams to create and implement complex clinical trials more effectively.

📋 Description

• Help design Faro's medical writing product for generating, reviewing and maintaining clinical trial documents from structured study design data • Serve as the medical writing voice in product development by translating authoring workflows, review cycles, regulatory expectations and writer pain points into product decisions • Establish quality criteria and review methods for AI-generated content, including scientific accuracy, consistency, traceability, narrative quality and expert judgment • Own the medical writing quality evaluation framework, including datasets, metrics, acceptance criteria, failure-mode analysis and comparison with expert-authored documents • Define content logic and authoring instructions for transforming structured study data into regulatory-grade narrative • Partner with selected customers to deploy authoring workflows, identify value and support adoption of human-in-the-loop processes • Partner with Implementation Services and Customer Strategy during pilot engagements and convert field learnings into reusable product capabilities • Support customer and commercial conversations about improving medical authoring with AI while preserving quality and trust • Identify medical writing work that can be simplified, automated or removed while preserving essential scientific and regulatory judgment

🎯 Requirements

• 7+ years of medical writing experience in pharmaceutical, biotechnology or CRO environments • Substantial responsibility for complex clinical and regulatory documents • Deep experience authoring and leading clinical trial protocols and protocol amendments • Experience with clinical study reports, investigator brochures or submission content strongly preferred • Strong understanding of clinical development and cross-functional inputs from Medical, Clinical Operations, Biostatistics, Regulatory, Safety and Data Management • Practical understanding of global regulatory expectations and document standards relevant to clinical development • Experience leading document review and reconciliation across multiple contributors • Ability to resolve inconsistencies and translate complex scientific decisions into clear written content • Ability to work directly with senior clinical and scientific stakeholders and earn trust through subject matter expertise • Bachelor's degree required in a life science, health science or related discipline • Practical experience using generative AI and LLM-based tools • Ability to test AI systems, evaluate outputs, identify failure patterns and determine improvements • Ability to distinguish scientific judgment from mechanical work and identify where human experts must remain in control • Comfort working with incomplete solutions and iterating quickly • Ability to move between detailed review and system-level workflow thinking • Clear communication with medical writers, clinicians, product managers and engineers • Comfort working directly with customers and supporting adoption of new workflows

🏖️ Benefits

• Equity will be a major component of total compensation • Health Care Plan (Medical, Dental & Vision) • Retirement Plan (401k) • Life Insurance (Basic) • Short Term and Long Term Disability • Paid Time Off (Flexible Vacation Policy; Paid Sick & Public Holidays Observed) • Training & Development Reimbursement • Hybrid Work Environment • Peer-to-peer bonus program • Company/department outings and events • Stock Option Plan • Office On-Premises Amenities; gym, restaurant tenant discount, Padel Nine (San Diego)