• You will profile and analyse businesses by collecting and processing their financials along with drawing up business, market, ownership and M&A track record overviews • You will form integrated views on platform and add-on deal opportunities for leading PE clients across Europe, with our technology supporting and enriching your insights • You will support research initiatives and learn about specific niche sectors we analyse on a weekly basis • You will gain first-hand insights in business development and project management, supporting various ad-hoc projects and contributing to platform improvements

• Collect, analyze, and synthesize intelligence from multiple disciplines including: HUMINT (Human Intelligence), SIGINT (Signals Intelligence), GEOINT (Geospatial Intelligence), OSINT (Open-Source Intelligence), IMINT (Imagery Intelligence) • Produce high-quality intelligence products including: Threat assessments, Area studies, Targeting packets, Pattern of life analysis, Intelligence summaries (INTSUMs), Daily and weekly intelligence reports • Support operational planning, mission execution, and force protection with real-time and predictive analysis. • Conduct trend analysis and predictive threat modeling. • Brief leadership and operational teams clearly and concisely. • Maintain situational awareness of regional security threats, actors, and geopolitical dynamics. • Integrate intelligence into operational planning cycles and commander’s decision-making processes. • Maintain strict adherence to classification handling, OPSEC, and intelligence oversight requirements.

The Head of Medical Writing will provide strategic and operational leadership for all Medical Writing activities to support BlueRock’s portfolio, from early development through product registration. Accountable for establishing and overseeing a cohesive, scalable Medical Writing function that delivers high-quality regulatory documents aligned with BlueRock’s global strategy, development timelines, and corporate priorities. Develop and lead an internal medical writing team, oversee vendor partnerships, and serve as a key strategic partner to various departments. Help shape future-state capabilities, including AI-enabled medical writing, platform-based content reuse, and collaboration models with Bayer colleagues. Define and own a Medical Writing strategy and roadmap aligned with BlueRock’s pipeline, regulatory milestones, and long-term growth. Establish standards, processes, and governance to ensure consistency, quality, and inspection readiness across all Medical Writing deliverables. Partner with Regulatory Affairs leadership to ensure integration of Medical Writing into regulatory strategy, Agency engagement, and submission planning. Drive a platform-based approach to document development for efficiencies and content reuse. Represent Medical Writing in cross-company forums as needed. Operational Excellence Provide oversight and accountability for all Medical Writing deliverables across BlueRock’s portfolio. Ensure delivery of documents that are on time, of high quality, and aligned with evolving global regulatory expectations. Identify opportunities to improve speed, quality, and scalability of document development. Lead resource planning (internal FTEs and external medical writing vendors) to support current and future program needs. Oversee and manage vendors and consultants to ensure consistent value, quality, and alignment. Serve as escalation point for complex document development challenges. Build, lead, and develop a high-performing internal Medical Writing team. Provide coaching, mentoring, and performance management to support professional growth and retention. Foster a culture of accountability, collaboration, and continuous improvement. Lead initiatives to modernize Medical Writing activities, including evaluation and pilot implementation of AI-enabled authoring, QC reviews, and content reuse tools. Define and manage collaboration models with Bayer, including potential shared services and/or AI-enabled pilots.

As Director of Clinical Trial Feasibility, Planning, and Analytics within Global Clinical Operations (GCO), you will play a pivotal role in shaping the future of clinical trials at BioNTech. Your work will directly contribute to optimizing operational planning and analytical support for global trials, ensuring alignment with our mission to revolutionize medicine through cutting-edge science. Lead feasibility assessments for global clinical trials, including site selection, patient population analysis, and competitive landscape assessment. Develop country and site-level enrollment projections and timelines, ensuring alignment with protocol design and core project team objectives. Build and maintain forecasting models to support scenario planning, resource allocation, and risk mitigation across the clinical portfolio. Provide operational input during the protocol design phase, ensuring trials are executable, cost-effective, and aligned with core project team objectives. Lead the adoption of advanced analytics, real-world data, and predictive modeling to inform feasibility and planning decisions. Lead implementation and optimization of digital tools and platforms to enhance planning accuracy and efficiency. Track clinical trial performance against expectations, identify areas for potential intervention, and advise cross-functional teams on clinical trial trade-offs across variables such as time, quality, and cost. Partner with CROs on ensuring alignment of assumptions and expectations around feasibility and performance of outsourced studies. Drive the evolution of BioNTech’s feasibility, planning, and analytics capabilities, strengthening internal ownership while optimizing the use of external partners. Establish and embed fit-for-purpose, cost-effective and scalable feasibility and analytics approaches that enhance internal decision-making. Serve as a key point of contact for clinical trial feasibility, planning, and analysis matters. Collaborate with peers in Clinical Operations and cross-functionally with Clinical Procurement, Vendor Management, Clinical Development, Medical Affairs, Regulatory and Project Management to support budgeting, resource planning, and trial prioritization. Participate in root cause analysis and develop mitigation strategies to address study execution and enrollment challenges. Ensure the quality and integrity of feasibility assessments and operational plans, actively identifying and managing internal and external risks. Support the QA team during internal audits, vendor audits, and/or hosting inspections as required. Adhere to the regulatory requirements, the ICH-GCP guidelines and the respective procedures (i.e. policies, SOPs, instructions).