Executive Director - Clinical Research Physician - GPS Medical

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. Clinical Research Physician, GPS Medical Purpose The Clinical Research Physician (CRP) in GPS Medical has responsibilities associated with the development, management, execution, and oversight of all aspects of the safety program for one (or more) asset(s) throughout the product(s’) life cycle. This individual plays a major role in coordinating technical functions within GPS to facilitate these responsibilities. The individual is accountable for collaborative contributions and partnership with the integrated development or product team to deliver on these safety commitments while demonstrating GPS expertise and leadership. The CRP is the Lilly GPS Medical representative for both internal and external stakeholders regarding a product or developmental therapeutic agent, interacting as prescribed in corporate guidelines, standards, and policies. Individualized responsibilities for a particular product or project will be discussed and agreed at an individual level. Primary Responsibilities This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Not all listed responsibilities will be applicable to all GPS Medical CRP roles. 1. Key GPS Medical Activities and Safety Oversight ▪ Provides GPS Medical leadership and ensures proactive pharmacovigilance (PV) for assigned product(s): i. In early phase development, performs and/or contributes to medical review of individual case safety reports for completeness and accuracy, providing company causality assessment and requests for follow up, if needed. ii. Provides medical oversight of surveillance activities, safety signal decisions and risk management actions to be taken, including communication and/or escalation to appropriate internal or external stakeholders (e.g., GPS leadership, governance committees, development teams, Regulators) iii. Monitors various safety activities for impact to Core Safety Information and Core Risk Minimization activities i v. Builds collaborative working relationships to ensure full cooperation; guides effective and efficient drug development, and ensures high-quality medical evaluation of safety data v. Responsible for the oversight and actions related to regulatory queries on safety-related topics ▪ Acts as the GPS Medical lead at the time of acquisitions and integrations of new companies/assets, partnering with internal and external stakeholders to ensure seamless continuity of safety surveillance activities. ▪ Demonstrates advanced knowledge of safety concepts, per ICH, US and international regulation/guidelines and GxP. ▪ Synthesizes complex data into actionable insights and translates technical issues into strategic discussions 2. Acts as the Lilly GPS Medical Representative for both internal and external stakeholders, interacting as prescribed in corporate guidelines and policies. ▪ Builds strong relationships with key stakeholders, representing and championing the role of safety in the organization (including): i. Product Team Leaders and Business Unit Leadership ii. Regulatory (including Device and CMC regulatory) iii. Affiliate Medical Leadership/Clinical Research Physicians iv. COE and Discovery and Clinical Research v. External Opinion Leaders ▪ Reviews and comments on external regulatory policy and trends affecting Global Patient Safety. ▪ Represents GPS Medical in inspection and audit activities for assigned program(s) ▪ May serve on safety advisory hub committees and/or consultative cross-functional bodies providing input and guidance to clinical development teams on select safety topics ▪ May serve as a member of the Quality-GPS (AE/PC and Device) safety surveillance teams evaluating aggregate product complaint/adverse event data for potential manufacturing quality related safety signals 3. Product Safety Assessment • Provide the sound and timely medical assessment decision making for the safety questions based on current medical and scientific data in collaboration with cross-functional partners for the following: i. Product Safety Assessments (PSAs), Health Hazard Evaluations (HHEs), and other risk assessment documentation ii. Device design, development, risk management, and periodic reporting iii. CMC development, manufacturing changes, CMC submissions and CMC regulatory requests, iv. Company anticounterfeiting activities, product shortage evaluations, quality triage escalation activities and regulatory reporting. ▪ Provide clinical evaluation of individual adverse events for possible manufacturing-related root cause for Lilly products ▪ Responsible for appropriate implementation of PSA/HHE process with manufacturing and/or marketing partners. ▪ Prepare medical complaints in response to signals identified during AE/PC and Device Surveillance. ▪ Review and approve/reject manufacturing investigation results in response to medical complaints, including escalation as needed for any identified manufacturing related safety issues. ▪ Proactive monitoring to evaluate for unanticipated safety impacts related to deviations addressed by HHEs 4. People Management ▪ Foster and support a collaborative working environment that maintains a Team Lilly culture focused on inclusion, innovation, acceleration, and delivery ▪ Recruit, mentor, develop, and retain top clinical, scientific, and drug development talent, including clinical research physicians, clinical research scientists, and pharmacoepidemiologists. ▪ Assures staff comply with company policies and procedures 5. Understand and support the QPPV role ▪ Understanding the roles and responsibilities of the European Union Qualified Person (QPPV). ▪ Ensure support is provided to enable the Qualified Person to fulfill all the Qualified Person legal responsibilities. 6. Training, Coaching, Mentoring ▪ Provide training, coaching and mentorship demonstrating effective PV strategies and sharing experience and knowledge to further advance the goals of the GPS department and wider enterprise. ▪ Maintain compliance with Lilly Red Book and corporate policies, Lilly Research Laboratories and Global Patient Safety curriculum. ▪ Maintaining compliance with the Lilly Corporate Integrity Agreement. 7. A Clinical Research Physician, GPS Medical is expected to meet the criteria as outlined in the global path job criteria for the appropriate R path levels. ▪ For each level on every global path, there is a consistent set of job criteria which includes functional and technical expertise, decision making, influence, and problem solving. Minimum Qualification Requirements: ▪ Medical Doctor or Doctor of Osteopathy. Must be board eligible or certified in appropriate specialty/subspecialty or have completed the comparable level of post-medical school clinical training relevant to the country of hirin