Summary

Summary The Evidence Generation Director is responsible for providing scientific leadership for all study types led by Global Medical Affairs including Phase IIIb/IV interventional trials, non-interventional studies, and Real-World Evidence programs ensuring they deliver innovative and scientifically robust evidence to the Global organization and key countries. By driving impactful evidence generation, this role enables informed decision making by regulators, payers, clinicians, and patients, ultimately supporting access, clinical adoption, and optimal use of our medicines.

The Evidence Generation Director contributes to the product medical strategy and is core contributor of integrated evidence planning. The incumbent will serve as an expert for evidence generation, enabling cross-functional teams to become leaders in developing and executing integrated evidence strategies.

This role requires excellent scientific and technical expertise in evidence generation across clinical trials and real-world settings as well as a strong understanding of product strategies, our business, and healthcare environments. Success also requires robust strategic thinking, leadership, collaboration and communication skills, as well as an entrepreneurial mindset, to work with and through others, to reimagine the way we use innovative evidence to develop and deliver medicines for patients.

The Director Evidence Generation will drive the development of integrated evidence approaches, techniques and standards as well as working closely with Biomedical Research, Development, International and key countries to enable innovative evidence.