Associate Director, Value and Scientific Communications

Scientific Writing & Deliverable Development 

• Independently lead, draft, revise, and finalize a broad range of high-quality scientific communication materials, including: 
• Peer-reviewed manuscripts for submission to scientific journals 
• Abstracts for scientific conferences 
• Scientific posters and slide decks for podium presentations 
• Tables, figures, and data visualizations 
• Help authors translate complex RWE and HEOR findings into clear, accurate, and compelling scientific narratives tailored to target audiences 
• Contribute to value dossiers, structured literature reviews, HTA submissions, and other value communication deliverables as needed 
• Correctly evaluate and interpret source documents (protocols, study reports, results tables) to develop outlines, appropriate tables, and figures 
• Ensure all deliverables meet the highest standards of scientific integrity, accuracy, and compliance with relevant guidelines (ICMJE, GPP, etc.) 
• Perform relevant searches of the clinical literature and summarize findings 
• Coordinate and complete journal and abstract submissions in adherence to submission guidelines and client templates 
• Provide copy editing, proofreading, and quality control reviews for other writers and researchers 
• Methodically incorporate author and reviewer comments to improve document accuracy and clarity 
• Address, revise, and clarify conflicting or ambiguous comments from authors and reviewers 

Project & Client Management 

• Independently manage multiple projects simultaneously, ensuring on-time, on-budget delivery with exceptional quality 
• Develop and maintain project timelines, track milestones, and proactively communicate project status to internal and external stakeholders 
• Coordinate cross-functional input from authors and internal research teams 
• Participate in and lead relevant internal and external team meetings, as well as client-facing project meetings 
• Manage existing and developing client relationships, including provision of strategic support, oversight of materials, post-submission support, and scientific advice 
• Participate in client capabilities presentations and support proposal development 
• Anticipate capacity issues and proactively identify solutions 

Team Leadership & Development 

• Mentor and support junior team members involved in writing projects 
• Lead and/or contribute to the development of templates, new ideas, and process improvements related to scientific communications 
• Assist in developing standards and processes, facilitate training opportunities, and provide consultation and resources to Genesis project teams 
• Share ideas for process improvement across the organization 
• Contribute to internal thought leadership projects 

Compliance & Professional Development 

• Maintain compliance with publication policies and procedures, including confidentiality, Quality Management System, secure file transfer, copyright law, and privacy protection 
• Develop familiarity with current industry practices, regulatory requirements, and guidelines that affect medical writing and value communications 
• Work across therapy areas to build knowledge of different study types and methods 
• Participate in training opportunities to enhance relevant skills and share learnings with the broader team 

• Master’s or PhD within a relevant life science, public health, or health economics-related discipline 
• 5+ years of industry or consulting experience in scientific/medical writing and/or evidence synthesis, across multiple project types and disease areas 
• Proven experience writing for the pharmaceutical industry, specifically in RWE, epidemiology, and/or HEOR 
• Strong attention to detail, clarity, and scientific accuracy 
• Excellent verbal and written communication skills 
• Strong organizational skills and ability to work independently in a deadline-driven environment 
• Excellent time and project management skills, including setting project goals, timelines, and budgeted hours 
• Proficiency in Microsoft Office (Word, PowerPoint, Excel) 
• Proficiency in EndNote for reference management 
• Proficiency in Adobe Creative Suite (Illustrator, InDesign, Acrobat Pro) 
• Ability to work collaboratively across multiple simultaneous projects and coordinate with various internal and external stakeholders 
• Ability to challenge diplomatically and appropriately 
• Demonstrates problem-solving skills and the ability to find and employ effective, creative solutions 
• Embrace change as an opportunity for growth and innovation; maintains a resilient and proactive attitude in a dynamic, growth-oriented environment 
• Demonstrate enthusiasm for learning and self-development, as well as a commitment to developing others 
• Preferred 
• Technical knowledge of the RWE, market access, and/or HEOR environment, with specific UK/European or US experience preferred 
• Experience with GraphPad Prism 
• Graphic design skills 

• Competitive salary 
• Performance-related bonus  
• Flexible Paid Time Off 
• Employer-matched pension plan 
• Private Medical Insurance