Responsibilities
* Contribute to study design by integrating pragmatic and decentralized elements aligned with clinical and product strategy
* Translate digital medicine strategy into actionable study-level plans, including selection of endpoints, technologies, and operational approaches
* Provide input on protocol design, feasibility, and patient‑centric approaches enabled by digital solutions
* Ensure alignment between digital design elements and study objectives, endpoints, and regulatory considerations
* Ensure successful implementation of decentralized trial elements (ePRO, wearables, remote monitoring, hybrid/virtual visits)
* Manage timelines, deliverables, and performance of digital/decentralized components across the study lifecycle
* Serve as the study‑level lead for digital medicine activities
* Partner with clinical study teams to embed and operationalize digital strategies
* Act as a key contributor in study planning discussions, bringing digital and DCT expertise
* Lead evaluation, selection, and oversight of digital health technologies and vendors
* Ensure vendor solutions align with protocol requirements and patient experience considerations
* Manage vendor performance, issue resolution, and delivery of milestones
* Collaborate with clinical operations, medical, regulatory, safety, and other functions
* Ensure digital components are fully integrated into broader study plans
* Stay current on evolving decentralized trial methodologies and digital health technologies
* Translate external trends into practical applications for study design and execution
* Support adoption of innovative approaches within study teams
* Communicate study design considerations, risks, and execution updates clearly
* Develop materials to support study teams and leadership discussions
* Influence stakeholders on adoption of pragmatic and digital approaches at the study level
Be part of our team. You would be joining a dynamic, successful and cohesive team dedicated to achieving results, continuously exploring innovative approaches to success, all while ensuring the delivery of the best medicines to benefit patients.
Required Qualifications
* Degree educated
* 5+ years of relevant clinical study management experience
Preferred Experience
* Minimum of 5 years of experience in clinical development, digital health, or related field, including leadership in DCTs and pragmatic trials. Preferably in cardiovascular, rare diseases, oncology and inflammation.
* Understanding of clinical trial operations, regulatory requirements, and digital health technologies.
* Experience of implementing digital strategies (ePRO, wearables, digital tools etc.) in clinical research at a global or regional level.
* Strong communication and stakeholder management skills; ability to influence across levels and functions.
* Post‑marketing / Phase 4 experience
* Experience with fully outsourced studies
It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever‑better products that reach over 10 million patients worldwide. It's time for a career you can be proud of. Join us.
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