Clinical Trials

Associate - Clinical Trials - Clinical Data page is loadedAssociate - Clinical Trials - Clinical DataApply locations US, Indianapolis IN time type Full time posted on Posted 7 Days Ago job requisition id R-91617At 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.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.**Please note, this is a hybrid position 3 days onsite/2 days remote**Purpose:This role is responsible for trial level clinical data strategy including database structure, content and meaning, acquisition, storage, retrieval, interchange, delivery and representation. This requires an in depth understanding of data collection, data flow management, data quality, data technology, dataset delivery, archiving and data standards. This role will collaborate with key study partners to define, implement, and deliver clinical data management packages. This role is responsible for providing trial leadership and ownership for a particular trial, set of trials, or programs.Primary Responsibilities:Portfolio Strategy, Planning and DeliveryDefine Lilly business requirements for the study/program for vendors to deliverEnsure that data management timeline and results are delivered to scope, cost, and time objectivesPerform project monitoring and quality oversight of sourcing providers for end-to-end data management activities – from study set up through trial execution through dataset deliveryEnsure vendor performance for the program-level flow of data, including across niche vendors and niche data sources (pharmacokinetic, immunogenicity, biomarker)Drives data flow design through consultation, review, and approval of vendor work. Ensures the data flow design is aligned with the project hypothesisApprove key outputs and results (i.e. Data Quality Delivery Plan, Data lock Plan, Project Plan, database, and observed datasets)Define and approve data quality and submission outputs and resultsProject ManagementEnsure that data acquisition, database design, and observed dataset requirements are reflective of specific protocol objectivesSpecifies the data collection tools and technology platforms for the trial/programDrive standards decisions, implementation and compliance for the study/programHelp create scope scenarios and negotiate outcomes with study teams while taking into account the cost and value of scenariosFacilitate/assimilate integration of disparate data sources into datasets for decision makingUse therapeutic knowledge and possess a deep understanding of the technology used to review data to ensure database deliverables are consistent and accurateEffectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to data deliverablesCommunicationAct as primary communication point for all data management activities related to a clinical study.Report out status of data management milestones and data quality.Partner with external data vendors: understand specifications to import multiple types of data, work with technical groups to ensure timely loads of external data sets into the sponsor's database.Demonstrate excellent written and verbal communication skills, including the ability to represent the Data and Analytics organization and influence stakeholders to drive data-driven decisions.Partner with cross-functional team members to ensure trial success through robust oversight/review.Process ImprovementContinually seek and implement means of improving processes to reduce cycle time and decrease work effortRepresent data sciences’ processes in multi-functional initiatives.Actively engage in shared learning across the Data and Analytics organization.Work with partners to increase vendor/partner efficienciesMinimum Qualification Requirements:Master’s degree in a scientific field such as Informatics/Analytics, Life Sciences, Statistics, Information Technology, Epidemiology, Computer Sciences (or Bachelor’s degree plus 3 or more years of experience in clinical data management or areas that closely intersect with clinical data management e.g., statistics, data analytics, information technology, health outcomes, etc...)Other Information/Additional Preferences:Demonstrated ability to set and implement plans to improve complex clinical data management processes and capabilitiesDemonstrated ability to effectively partner/influence a remote team and drive a technical project to deliver resultsExperience with application of clinical data management skills such as data flow, data quality & integrity, data interchange, data mining, and data representation principlesDemonstrated ability to lead development of creative data solutions to address clinical development challengesPassionate about improving technological solutions using new technologiesSociety of Clinical Data Management certificationWorking knowledge of programming languages & Industry tools such as Tableau, PowerBI, Python, SAS, ‘R’ and Shiny for reporting, metrics and visualizations along with P-SQL, T-SQL for DBMS.Experience with the following:Articulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutionsUtilization of clinical/drug development knowledge and an ability to collaborate closely effectively with study team members (i.e. Statistics, PK, Operations, Medical)Strong therapeutic/scientific knowledge in the field of researchKnowledge of medical terminologyDomestic and International travel may be requiredAbility to balance multiple activities, prioritize and manage ambiguityDemonstrated exemplary teamwork/interpersonal skillsDemonstrated problem solving, attention to detail and result oriented behaviors in a fast-paced environment.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 is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is$63,000 - $140,800Full-time equivalent employees 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 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care 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).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 employees.#WeAreLillySimilar Jobs (5)Clinical Study Build Programmerlocations US, Indianapolis IN time type Full time posted on Posted 28 Days AgoAssociate Director – Clinical Trial Foundations (P4) - Digital Trial Foundationslocations US, Indianapolis IN time type Full time posted on Posted 8 Days AgoClinical Study Build Programmer - eCOAlocations US, Indianapolis IN time type Full time posted on Posted 30+ Days AgoAt Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world.How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe #J-18808-Ljbffr