Director, RWE, CMH

## Director, RWE, CMHApplylocations:
Canada, Ontario time type:
Full time posted on:
Posted Todayjob requisition : R
- At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.

We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
** Position Summary
** The RWE Director is responsible for driving the Real-World Evidence strategy and execution within Medical Affairs in collaboration with the therapeutic area. This role will ensure that robust, high-quality evidence is generated and communicated to inform clinical practice, regulatory/payer decisions, and healthcare policy, while addressing critical data gaps across the product lifecycle. The RWE Lead partners cross-functionally with Medical, Clinical Development, HEOR, Market Access, and external stakeholders to position the company as a scientific leader and trusted partner in improving patient outcomes.

This is a hybrid role – onsite presence at our Toronto office will be 10 days or more per month (or at least 50% of the time), determined in collaboration with your manager and based on business needs.

At Lilly Canada, we have three levels for this position based on the candidate’s experience, background, and qualifications. The expected compensation is:

Advisor: $117,750 – $172,700

Senior Advisor: $129,750 – $190,300

Director: $142,500 - $209,000

This role is eligible for additional forms of compensation, such as participation in the Lilly Bonus Program. This posting is for an existing vacancy.
** Key Responsibilities
**** Evidence Strategy & Leadership
*** Collaborate and align with Sr. Medical Director/Director/Medical Advisor to develop the integrated evidence generation strategy for assigned therapeutic area(s), aligned with global/regional medical plans and corporate priorities.
* Prioritize and address evidence gaps related to disease burden, treatment patterns, patient outcomes, safety, and comparative effectiveness.
* Ensure evidence plans meet the needs of regulators, payers/HTA, healthcare professionals, and patients.
** Study Design & Execution
*** Lead the design development, execution, and oversight of observational studies, registries, pragmatic trials, external control arms, database studies, and patient-reported outcome research.
* Manage vendor/CRO partnerships for study execution, ensuring quality, compliance, and timely delivery.
* Oversee due diligence and utilization of real-world data (RWD) assets including EMR, claims, registries, and digital health data.
** Cross-Functional & External Collaboration
*** Partner closely with HEOR, Market Access, Regulatory, Clinical Development, Pharmacovigilance, and Commercial Insights to ensure evidence addresses cross-functional needs.
* Serve as the Medical Affairs RWE point of contact for internal stakeholders, training teams on RWE interpretation and application.
* Support Sr. Medical Director/Director/Medical Advisor in engagements and interactions with KOLs, academic collaborators, patient registries, and external data consortia.
** Communication & Dissemination
*** In collaboration with Sr. Medical Director/Director/Medical Advisor drive dissemination of RWE through publications, congress presentations, dossiers, and educational activities per overall therapeutic area congress strategy.
* Ensure scientific integrity, compliance (GPP, GCP, SOPs), and transparency in all outputs.
* Provide RWE insights to inform medical education, payer submissions, label expansion, and health policy discussions.
** Team & Capability Development
*** Provide mentorship to junior RWE scientists and medical team members.
* Champion innovation in data science, analytics platforms, and digital RWE solutions.
* Contribute to enterprise-wide RWE governance, standards, and capability building.
**…