Associate Director Real World Evidence

Role Overview: As an Associate Director Real World Evidence, you will report to the Global Head of Real World Evidence Oncology and play a crucial role in shaping RWE use in oncology to enhance decision-making and value creation. Key Responsibilities: - Act as the functional product lead and subject matter expert (SME) for assigned product(s) - Lead RWE strategy for Integrated Evidence Plans (IEP) - Lead execution of RWE strategy for product(s) - Lead identification and selection of fit-for-purpose RWD sources for given research questions and contribute to the RWD strategy of the assigned product(s) therapeutic area - Act as study lead for Non-Interventional Studies (NIS) - Lead crossfunctional analysis requests - Provide SME to product team meetings and other key internal strategic meetings - Develop epidemiological sections for submission relevant documents - Participate in and contribute to HA interactions - Provide high-quality input to critical review assessments, expert statements, publications, and study proposals - Lead Business Plan initiatives and ensure effective implementation - Promote communication, set up adequate information flows, and ensure stakeholder alignment for projects and activities - Lead process improvement according to lean concepts aiming for simplification - Contribute to the implementation of Scientific Best practices within the function and the company in general - Act as a mentor for less senior RWE scientists Qualifications Required: - Masters or Doctoral degree, or PhD in (pharmaco)epidemiology, public health, or biostatistics - Comfortable in Business English - 5-8 years of (pharmaco)epidemiological experience preferred in the Pharmaceutical/ Biotechnology Industry, academic setting, in CROs - Demonstrated experience in studies using RWD - Strong methodological and design skills; epidemiology study designs/ analysis. Medical/ pharmacological/ pharmacovigilance knowledge would be a plus - Experience of project management in studies life cycle, preferably exposed to a multi-cultural environment - Comprehensive expertise in drug development, including knowledge of interfaces and interdependencies of clinical development with other functions - Experience of the regulatory environment and of standards used in our field (GPP, GVP, ENCePP) Additional Company Details: The company is committed to diversity and believes that it drives excellence and innovation, strengthening the ability to lead in science and technology. They are dedicated to creating access and opportunities for all individuals to develop and grow at their own pace. Join a team that is focused on Sparking Discovery and Elevating Humanity!,