Medical Writer, GCS Creative Services
Wilmington, DE - USA
Job Summary
Are you driven to turn complex science into narratives that change decisions for healthcare professionals and improve life for patients Do you thrive at the intersection of scientific rigor creative storytelling and rapid delivery at scale As the senior scientific content authority within GCS Creative Services you will shape the scientific voice behind our most visible HCP patient and internal communications. You will partner closely with a Creative Lead and an Experience Lead from intake to final delivery ensuring every word is accurate compliant on-brand and designed for the channel and audience at hand. Your work will help clinicians understand evolving evidence empower patients to engage in their care and enable our internal teams to deliver on bold ambitions across therapy areas.
This is a role for a medical writer who moves with agency-caliber pace and polish can pivot seamlessly from congress updates to MLR-ready copy and enjoys orchestrating content with distributed studio teams. You will build the frameworksmessaging maps claims substantiation and modular contentthat power consistent scalable storytelling across our portfolio.
Accountabilities: Scientific Content Development: Lead the creation review and maintenance of high-quality scientific materialsnarratives MSL resources infographics FAQs and multi-format assetsthat inform and engage HCPs and patients across therapeutic areas. Creative Partnership: Collaborate with the Creative Lead from intake through delivery to merge scientific clarity with visual storytelling. Shape content hierarchy structure and layout to maximize comprehension and impact.
Experience Alignment: Work with the Experience Lead to align content with brand priorities editorial calendars and stakeholder expectations. Support intake responses scope content requirements and manage timelines to hit critical milestones. MLR Excellence and Compliance: Prepare and submit MLR-ready packages with full claims substantiation accurate referencing fair balance ISI placement and rigorous version control. Address copy and evidence-related comments to secure timely approvals. Evidence Strategy and Reference Management: Conduct targeted literature searches assess data quality select and track references ensure traceability between claims citations and copy across versions and channels.
Multi-Audience Multi-Channel Strategy: Develop and adapt content for DTC/patient DTP HCP promotional and educational medical/scientific and market access deliverables. Tailor tone reading level and depth to each audience and channel. Scientific Interpretation and Synthesis: Translate clinical studies endpoints statistical analyses guidelines and real-world evidence into precise compelling narratives. Rapidly synthesize congress updates and publications into concise summaries and key messages for in-market assets. Brand Voice and Editorial Governance: Uphold AstraZenecas brand voice and editorial standards. Elevate clarity accessibility and inclusivity while proofreading and editing for grammar style data integrity and regulatory alignment.
Agile Delivery and Studio Coordination: Operate within an agile model managing content workstreams through iterative cycles. Provide direction annotations and quality oversight to near-shore studio teams for accurate copy and layout execution at scale. Content Standards and Governance: Maintain templates glossaries style guides and taxonomies aligned to GCS standards. Advance best practices for routing file hygiene modular content development and content reuse.
Creative Briefing and Concepting: Contribute to reverse briefs ideation and creative reviews alongside Creative and Experience Leads. Provide scientific perspective and feasibility guidance early in the process to de-risk execution. Quality Assurance and Review: Serve as the final quality checkpoint for all written content prior to MLR and stakeholder delivery ensuring scientific accuracy citation integrity brand alignment and compliance readiness.
AI-Enabled Efficiency: Support AI initiatives in content creation. Use AI-assisted writing and research tools to accelerate development while maintaining scientific rigor and regulatory compliance.
Mentorship and Capability Building: Coach junior writers and near-shore partners on scientific storytelling referencing standards MLR expectations and emerging formats and channels. Foster a culture of scientific excellence and continuous improvement.
Essential Skills/Experience:
7 years in medical writing or healthcare copywriting within pharmaceuticals biotechnology medical devices or regulated healthcare communications
Bachelors degree in Life Sciences Pharmacy Medicine Communications or related field
Extensive experience in pharmaceuticals or biotechnology with deep familiarity with DTC DTP HCP medical content and market access requirements
Hands-on experience preparing submitting and revising MLR packets with fluency in claims mapping reference standards fair balance and promotional labeling constraints
Demonstrated ability to interpret clinical studies endpoints statistical analyses and clinical guidelines and translate them into accurate compelling narratives for HCP and patient audiences - Proven multi-channel portfolio spanning digital (email web social CRM banners) sales enablement (detail aids slide kits) congress materials and select print with understanding of channel specifications and accessibility best practices
Strong client-facing and cross-functional communication skills; confident presenting work synthesizing feedback and driving alignment with Creative Leads Experience Leads brand teams and medical affairs stakeholders
Experience operating within agile or iterative delivery models managing content workstreams through sprint-based or rapid-cycle environments
Proficiency with reference management and annotation practices; familiarity with project management tools (e.g. Workfront JIRA ) collaboration platforms and DAM systems
Working knowledge of AI-assisted writing and research tools
Meticulous approach to grammar style citations and version control; proven ability to manage multiple concurrent projects with tight timelines while maintaining scientific accuracy and quality
Experience maintaining or contributing to style guides glossaries content templates and modular content frameworks
Desirable Skills/Experience:
Agency experience with demonstrated ability to operate at pace and quality standards
Experience coordinating with distributed or near-shore production teams
Advanced degrees (e.g. PharmD PhD MPH MSc)
Experience developing messaging frameworks claims maps and MLR-ready content packages across a portfolio
Why AstraZeneca: Here scientific knowledge meets bold commercial execution to deliver solutions that matter to patients. You will work in a high-trust high-autonomy environment where scientists creatives and data experts sit together to spark ideas start small and scale fast. We connect across the healthcare ecosystem to identify where communication can make the biggest differenceclarifying evidence accelerating understanding and improving decisions across the patient journey. Expect pace thoughtful risk-taking and genuine collaboration; we value kindness alongside ambition. Your craft will help translate breakthrough evidence into action contributing to real outcomesincluding progress that is already changing the trajectory of serious disease.
Call to Action: If youre ready to lead the scientific story that moves clinicians and patients to better outcomes step forward and show us how you will raise the bar!
Date Posted
15-Jun-2026Closing Date
28-Jun-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and furtherance of that mission we welcome and consider applications from all qualified candidates regardless of their protected characteristics. If you have a disability or special need that requires accommodation please complete the corresponding section in the application form.
About Company
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, ... View more