Do you have a passion for clinical trials? Are you experienced in the management of clinical trial sites? Is exceptional customer and patient care important to you? If so, then we have the role for you.
The Clinical Development Consultant (CDC) is responsible for the management of clinical sites being considered and/or participating in Lilly clinical trials; inclusive of site identification and qualification, the timely delivery of clinical trial enrollment in accordance with scientific objectives, timely delivery of database locks, issues management at clinical trial
sites, and ensuring inspection readiness at all times for assigned therapeutic area(s) within a region/country that enables global program delivery. In this role, you will have accountability for comprehensive site management, leveraging of information/tools to make/have informed decisions and discussions, and high quality interactions with global clinical trial sites to drive to an unparalleled customer experience. Additionally, you will be responsible for oversight of vendor monitoring activities at the sites, including the identification, mitigation and escalation of significant findings and trends. Additional local responsibilities may be required as needed/appropriate for the local geography.
Clinical Investigator Management
Accountable for activities required at clinical trial sites by investigators and site staff participating in Lilly trials
Accountable for comprehensive site management activities to ensure timely delivery of enrollment readiness, trial recruitment/enrollment and database locks
Responsible for identifying potential opportunities to accelerate trial enrollment, while driving to an unparalleled clinical trial/customer experience
Accountable for the application of scientific, therapeutic area, and institutional/regional expertise to inform and ensure timely delivery of trial enrollment and quality data
Responsible for the development of strategic institutional/site relationships to optimize the delivery of clinical trial programs; including across therapeutic areas where applicable
Clinical Trial Management
Responsible for the development and implementation of applicable site risk plans to ensure delivery of clinical trial enrollment commitments and database locks
Ensure site and country level inspection readiness at all times
Utilize metrics to inform site/country/regional level decision making
Work with internal and external groups to remove barriers to trial execution at a site and/or country level
Responsible for understanding local treatment paradigms and standard of care to support targeted feasibility and strategic allocation of trials as required
Provide vendor oversight for site monitoring activities at site/country level
Business Management and Engagement
Establishes and develops strong professional relationships with active/potential clinical investigators to expand/maintain clinical research partnership opportunities and provide an unparalleled experience for participation in Lilly clinical trials.
Cross functional collaboration and partnership to ensure alignment in priorities and deliver the portfolio
Perform targeted sites prospecting in alignment with portfolio strategy & priority
Maintain therapeutic and technical expertise to enable scientific discussions with the investigator and site personnel
Serve as an effective communication
Internal Number: 49245
About Eli Lilly & Company
Company Overview 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 39,000 employees worldwide 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.