INTRODUCTION & ROLE PURPOSE

Acumetis was born from the union of leaders in life sciences strategy and patient-focused solutions. Together, we combine decades of experience across scientific insights, commercial strategy, launch excellence, and healthcare innovation to tackle the complex challenges that shape the future of medicine. We partner with leaders to solve high-stakes problems, uncover hidden opportunities, and translate scientific, clinical, and health economic evidence into actionable insights. By connecting expertise across functions, life sciences organisations can make smarter decisions, strengthen value communication, and deliver therapies to the patients who need them most. When you reframe what’s possible, scientific evidence becomes meaningful insight, complex data becomes compelling narratives, and innovation reaches the people who need it most.

As a Senior Manager, you will play a pivotal role in leading medical writing and HTA-focused engagements across the pharmaceutical, biotechnology, and healthcare sectors. At this level, you are expected to demonstrate advanced scientific leadership, deep expertise in medical writing through demonstratable experience of having supported HTA submissions, value proposition development, publication writing and market access strategy and evidence synthesis-associated written deliverables.

Senior Managers own large programmes end-to-end, ensuring excellence across scientific communications, HTA submissions, value evidence development, and publication strategy while managing cross-functional teams and maintaining strong client partnerships. You will influence internal thinking, shape scientific methodologies, and provide leadership that strengthens Acumetis' scientific communications and market access capabilities.

This role requires advanced leadership, scientific credibility, and a passion for translating complex evidence into clear, impactful communications for diverse audiences including HTA agencies, payers, healthcare professionals, policymakers, and industry stakeholders. This role builds the capabilities required for progression to Associate Director, where strategic ownership of major client accounts, scientific leadership, commercial responsibility, and thought leadership become core expectations.

ROLE RESPONSIBILITIES AND EXPECTATIONS

Core Knowledge

Lead the development of high-quality medical writing deliverables across HTA, market access, and evidence synthesis projects, ensuring scientific accuracy, strategic alignment, and clear communication of complex evidence.

Author and review a range of written outputs, including HTA submission materials, value dossiers, value propositions, evidence summaries, publication manuscripts, and other market access and evidence-generation-related deliverables.

Translate complex clinical, economic, and real-world evidence into compelling, stakeholder-focused narratives tailored to payer, HTA, healthcare professional, and industry audiences.

Embed Medical Writing, HTA, and Market Access expertise into client engagements, ensuring deliverables effectively communicate evidence and support strategic decision-making.

How You Work

Critical Thinking & Attention to Detail

Drive strategic scientific decision-making across programmes, balancing evidence requirements, stakeholder expectations, and client objectives.

Review scientific deliverables across teams, establishing and reinforcing quality assurance standards and best practices.

Guide teams through complex evidence challenges, shaping clear scientific narratives and strategic recommendations.

Time Management & Collaboration

Manage priorities across multiple client engagements, publications, HTA projects, and evidence-generation workstreams.

Coordinate resource planning and delivery timelines across scientific and consulting teams.

Build strong collaboration across Medical Affairs, HEOR, Market Access, Clinical Development, and Commercial functions.

Lead the development of a high-performance culture through strong scientific leadership and collaboration.

Communication & Client Engagement

Lead scientific workshops, evidence-planning discussions, HTA strategy meetings, and advisory board engagements.

Act as a trusted scientific advisor to clients, navigating complex stakeholder discussions with confidence and credibility.

Communicate scientific and value-based evidence in a way that supports informed decision-making among senior stakeholders.

Project Management

Oversee scientific programmes, ensuring alignment across scope, budgets, teams, timelines, and quality standards.

Review and approve evidence-generation, literature review, and medical writing approaches across workstreams.

Coordinate multiple parallel projects while maintaining delivery excellence and client satisfaction.

Ensure consistent project forecasting, compliance, and operational visibility.

What You Do

Research & Evidence

Lead evidence reviews and synthesis activities across multiple therapeutic areas and client programmes.

Develop evidence frameworks that support HTA submissions, payer engagement, scientific publications, and value communications.

Provide methodological guidance on literature reviews, evidence generation, and research approaches.

Analysis & Strategic Interpretation

Review clinical, epidemiological, outcomes, and health economic evidence to ensure scientific robustness and strategic value.

Integrate clinical data, HTA requirements, market dynamics, and policy considerations into clear client recommendations.

Writing, Storytelling & Deliverables

Provide senior review and strategic oversight of HTA dossiers, value communications, manuscripts, abstracts, posters, slide decks, and scientific reports.

Develop compelling evidence-based narratives tailored to payers, HTA bodies, healthcare professionals, and internal stakeholders.

Ensure accuracy, compliance, consistency, and scientific excellence across all written deliverables.

Champion best practices in medical writing, publication standards, and scientific communication.