Our Medical Affairs specialists bring unparalleled expertise and sector knowledge to champion your products every step of the way – from successful preparation for launch to effective life cycle management. At tranScrip, we excel in empowering our clients through a comprehensive array of pre- and post-launch Medical Affairs initiatives across multiple therapeutic areas, including rare diseases, bridging the gap between scientific innovation and clinical practice to improve patient outcomes.
Throughout the life cycle of your product, our robust Medical Affairs package ensures that your strategic planning and programme execution is not just comprehensive but transformative.
Maximise the value of your products with our bespoke solutions.
We help you to drive operational excellence of your Medical Affairs function by advising on optimal organisation, resourcing, and vendor management, through coaching, mentoring and SME consultancy.
Our team excels in crafting comprehensive Medical Affairs strategies that align with your business objectives across therapy areas, creating purpose-built tactical plans that enhance market access and product life cycle management.
We identify key stakeholders in the healthcare ecosystem, including clinicians, researchers, patient advocacy groups, and regulatory bodies. Our influence mapping techniques and stakeholder management planning help to prioritise engagement efforts and shape the external environment.
Our expertise extends to the meticulous planning, design and support for execution of late-stage clinical trials and RWE programmes. We ensure that your studies are designed to meet regulatory requirements, generate robust data, and support the optimal use and value proposition of your product.
Through medical insights generation planning, advisory boards, expert panels and 1:1 expert interviews, enhanced by the appropriate use of AI tools, we transform complex scientific data into actionable insights and clear, concise, and impactful messaging.
Our experienced teams work with you and your external experts to create compelling narratives that accurately convey your data and insights and resonate with both medical professionals and broader audiences, delivered through publications in leading journals, conference presentations and satellite symposia, and training programmes.
Our teams collaborate closely with your global headquarters and local teams to craft and implement robust and compliant Medical Affairs strategies. We facilitate seamless interactions with external experts and opinion leaders, fostering productive cross-functional collaboration within and outside your organisation.
Executive Director Medical Affairs, Regional Medical Lead, Hemato Oncology (Europe)
BeiGene
Our experienced physicians and scientists, together with our regulatory, clinical and commercial experts can support you to maximise the value of your products. Whatever your project requires, we have the expertise to meet your needs.
