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.

The Clinical Development Consultant (CRL) 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. This is achieved by the CRL’s 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 unparallel customer experience. The CRL is also responsible for oversight of vendor monitoring activities at clinical trial 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 and by investigators and site staff participating in Lilly trials; inclusive of site identification and qualification, enrollment planning and execution, to database lock and close outAccountable for comprehensive site management activities to ensure timely delivery of enrollment readiness, trial recruitment/enrollment and database locks; inclusive of performance management and issue mitigation, identification and resolutionResponsible for identifying potential opportunities to accelerate trial enrollment, while driving to an unparalleled clinical trial/customer experienceAccountable for the application of scientific, therapeutic area, and institutional/regional expertise to inform and ensure timely delivery of trial enrollment and quality dataAccountable 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 locksEnsure site and country level inspection readiness at all timesLeverage metrics to inform site/country/regional level decision makingWork with internal and external teams to remove barriers to trial execution at a site and/or country levelResponsible for understanding local treatment paradigms and standard of care to support targeted feasibility and strategic allocation of trials as requiredProvide 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 portfolioPerform targeted sites prospecting in alignment with portfolio strategy & priorityMaintain therapeutic and technical expertise to enable scientific discussions with the investigator and site personnelServe as an effective communication “bridge” between sites, third party vendors and LillyInfluence and challenge internal and external factors in order to improve clinical research delivery

Minimum Qualification Requirements:

Bachelor’s degree or equivalentMinimum of 8- 10 years’ experience in the pharmaceutical industry and/or clinical research and strong working knowledge of Good Clinical PracticeTherapeutic expertise and knowledge of the clinical research landscape; ability to acquire and maintain therapeutic expertise to support portfolio needsStrong self-management and organizational skills; ability to manage workload, set personal priorities and adjust as neededDemonstrated strategic agility & broad business acumenDemonstrated leadership behaviours with ability to accept challenges, seek opportunities to remove barriers, influence without authority, and lead in areas of uncertainty

Other Information/Additional Preferences:

Strong preferences for bachelor’s degree in scientific or health-related fieldStrong communication (both verbal and written) and language skillsStrong organizational/planning skillsDemonstrated ability to enhance/improve customer experience Fluent in English as well as required language to conduct day-to-day businessStrong knowledge in country regulatory guidelines/requirementsStrong teamwork and interpersonal skillsDemonstrated decision-making abilityAbility to develop and apply creative solutionsTravel required (50-75%

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

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