Join American pharmaceutical leader Eli Lilly and Company, currently hiring Associate Director Clinical Development (North Carolina, Virginias, Maryland) in Indianapolis, Apply Lilly careers in Indianapolis Indiana.
Position : Associate Director Clinical Development (North Carolina, Virginias, Maryland)
Location : Indianapolis, Indiana
Job id: R-27477
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 35,000 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.Organization Overview:At Lilly, we serve an extraordinary purpose. For more than 140 years, we have worked tirelessly to discover medicines that make life better. These discoveries start in Lilly Research Laboratories, where our scientists work to create new medicines that will help solve our world’s greatest health challenges.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 on time delivery of clinical trial enrollment in accordance with scientific objectives, on time 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 CDC’s accountability for comprehensive site management, maximizing 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. The CDC is also responsible for oversight of vendor monitoring activities at clinical trial sites, including the identification, mitigation and escalation of significant findings and trends.Responsibilities:Clinical Investigator ManagementAccountable 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 on time 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 advise and ensure on time 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 ManagementResponsible 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 timesUse metrics to advise 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 EngagementEstablishes 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 a liaison between sites, third party vendors and LillyInfluence and challenge internal and external factors in order to improve clinical research deliveryBasic Requirements:Bachelor’s degree or equivalentMinimum of 3 years’ experience in the pharmaceutical industry and/or clinical researchAdditional Preferences:Strong working knowledge of Good Clinical PracticeStrong preferences for Bachelor’s degree in scientific or health-related fieldTherapeutic 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 acuityDemonstrated leadership behaviors with ability to accept challenges, seek opportunities to remove barriers, influence without authority, and lead in areas of uncertaintyDemonstrated problem solving, attention to detail and result oriented behaviors in a fast-paced environment.Strong communication (both verbal and written) and language skillsStrong organizational/planning skillsDemonstrated ability to enhance/improve customer experienceFluent 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 solutionsPrevious experience in Diabetes, Cardiometabolic, and/or Weight managementGeography includes but not limited to: North Carolina, Virginias, Maryland (need to reside in the geography)Additional Information:Travel required (50-75%)Lilly currently anticipates that the base salary for this position could range from between $103,5000 to $152,000 and will depend, in part, on the successful candidate’s qualifications for the role, including education and experience. This position also will be eligible for a company bonus(depending, in part, on company and individual performance).In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored retirement plan and 401(k); vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent daycare flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Of course, the compensation described above is subject to change and could be higher or lower than the range described above. Further, Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employeeEli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.
Lilly is an EEO/Affirmative Action Employer and 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.
As a condition of employment with Eli Lilly and Company and its subsidiaries in the United States and Puerto Rico, you must be fully COVID-19 vaccinated and provide proof of vaccination satisfactory to the company (subject to applicable law).
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