Source Job

• Leads writing and preparing clinical and regulatory documents for drug and device development.
• Coordinates review, approval, and quality control across functions to ensure compliance and timelines.
• Develops knowledge of US and international regulations and participates in process improvements.

AbbVie discovers and delivers innovative medicines and solutions addressing serious health issues in immunology, oncology, neuroscience, and aesthetics. They are a large global biopharmaceutical company committed to having a remarkable impact on people's lives.

• Lead authoring and development of high-complexity Phase II-IV clinical regulatory documents for a top pharma partner.
• Own the end-to-end medical writing process from planning through final delivery, ensuring alignment with strategy and timelines.
• Coordinate cross-functional teams across geographies and facilitate comment resolution to drive document development.

Fortrea delivers solutions that bring life-changing treatments to patients faster. They are a global organization that empowers employees to shape their own career path with comprehensive training and management support.

• Author clinical study reports, protocols, informed consent forms, narratives, and investigator brochures across therapeutic areas.
• Represent Medical Writing at meetings, drive document development, and articulate strategy and timelines.
• Mentor junior staff, manage multiple priorities, and foster collaboration to resolve conflict.

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, the company has a fast-growing, science-driven culture and is recognized as a Great Place to Work in 2021, among other awards.

• Create original medical documents such as clinical reports, case studies, and research papers to support AI training.
• Ensure materials meet strict standards of accuracy, clarity, and educational value while de-identifying confidential information.
• Collaborate remotely with project teams to curate diverse documentation sets for varied AI training use cases.

Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. They use AI to review applications and match top-fitting candidates to roles, operating as a project-based contractor facilitator.

• Develop and review medical response documents with scientific accuracy and editorial excellence.
• Perform source-to-output verification, validate references, and ensure consistency across deliverables.
• Support MLR readiness through quality checks aligned with FDA guidance, AMA style, and ICMJE standards.

EVERSANA creates next-generation commercialization services for the life sciences industry. Their global team of over 6,000 employees serves more than 670 clients, from biotech start-ups to pharmaceutical companies, and embraces diversity and inclusion.

• Write clear and concise medical copy for HCPs and patients, adhering to ABPI guidelines and quality processes.
• Collaborate with strategy, creative, and account teams to develop effective campaigns.
• Manage projects from concept to completion, ensuring timelines and quality standards.

Real Chemistry is a global healthcare communications and marketing agency that partners with top pharmaceutical and biotech companies. The company fosters a culture of innovation and collaboration, with over 5 years of growth, and has been certified as a Great Place to Work.

• Write end-to-end flows and in-product copy across the app, including interface text, states, onboarding, system messaging, and error language.
• Design features alongside designers and product from concept, shaping copy and layout together.
• Own naming, terminology, voice, and tonal guidance for features and AI-generated content.

webAI is pioneering distributed AI infrastructure for personalized, edge-based artificial intelligence, keeping data private and secure. The team is driven by truth, ownership, tenacity, and humility, and is building an end-to-end platform for enterprise AI.

• Provide subject matter expertise to teams for global disclosure strategies of clinical documents under regulatory requirements.
• Manage planning, preparation, and quality control for disclosures, including oversight of vendor deliverables.
• Lead development of standard processes and technological solutions to ensure compliance with disclosure regulations.

Pfizer is a global biopharmaceutical company dedicated to discovering and developing innovative therapies. As a large multinational employer with a culture of individual ownership, it employs tens of thousands of people and fosters a collaborative and inclusive environment.

• Drive growth of Regulatory Science and Medical Writing services across pharmaceutical, biotechnology, and life sciences clients.
• Lead strategic sales efforts, identify client needs, and partner cross-functionally to deliver tailored solutions supporting regulatory approvals.
• Serve as the primary liaison between client and company for all sales-related activities, enhancing visibility and market presence.

Veristat accelerates life-changing therapies to patients worldwide with more than 30 years of expertise. They have a flexible, inclusive culture with 70% remote workforce and 66% women-led teams, having prepared over 105 approved therapies and delivered over 350 rare disease projects.

• Develop scientific copy for various deliverables on assigned brands and products.
• Work independently and collaboratively with medical writers and directors to develop scientifically accurate copy.
• Manage workflow for assigned projects and meet associated deadlines.

Real Chemistry is a global agency providing a full suite of services across healthcare communications and marketing to top pharmaceutical and biotech clients. They foster a culture rooted in being best together with a commitment to excellence, offering a comprehensive benefits program and perks.

• Define the product strategy and core user journeys for an AI-assisted long-form writing platform.
• Drive intuitive interfaces for complex AI capabilities like multi-chapter drafting and compliance workflows.
• Own global scaling of digital distribution and print-on-demand networks across international markets.

DreamBook is an AI-driven publishing platform that turns ideas into globally distributed books. It is built by Meraki Labs, a venture studio founded by Mukesh Bansal, known for its fast-paced, high-agency culture.

• Produce clear, accurate documentation for complex AI and analytics software products, using tools like Markdown, DITA, or XML.
• Collaborate with cross-project teams to deliver content that maximizes usability and enhances customer experience.
• Possess expertise in generative AI, agentic AI, RAG, and LLMs to support in-solution AI chatbots and content production.

SAS is a leader in data and AI, inspiring customers worldwide to transform data into intelligence. Recognized for an inclusive culture and innovative technologies, it offers a world-class employee experience.

• Produce high-quality content for diverse medical communications projects, demonstrating excellent scientific understanding.
• Develop content with minimal supervision, within budget and on time, using client approval systems.
• Attend conferences, present work to clients, and manage day-to-day client communication and relationships.

Lumanity is dedicated to improving health outcomes by accelerating and optimizing access to life-changing medicines. As a global strategic partner, they bring together strategy, evidence, engagement, and technology to engineer breakthrough value.