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Lilly Clinical Data Associate in Alcobendas, Spain

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.

Stats Data and Analytics organization (SDnA) lead Lilly to achieve innovative scientific and operational excellence in design, analysis, and interpretation to improve patient outcomes

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 Delivery

o Define Lilly business requirements for the study/program for vendors to deliver

o Ensure that data management deliverables are delivered to scope, cost, and time objectives

o Execute project monitoring and quality oversight of sourcing providers for end-to-end data management activities – from study set up through trial execution through dataset delivery

o Ensure vendor performance for the program-level flow of data, including across niche vendors and niche data sources (pharmacokinetic, immunogenicity, biomarker)

o Drives data flow design through consultation, review, and approval of vendor work. Ensures the data flow design is aligned with the project hypothesis

o Approve key deliverables (i.e. Data Quality Delivery Plan, Data lock Plan, Project Plan, database, and observed datasets)

o Define and approve data quality and submission deliverables.

Project Management

o Ensure that data acquisition, database design, and observed dataset requirements are reflective of specific protocol objectives

o Specifies the data collection tools and technology platforms for the trial/program

o Drive standards decisions, implementation and compliance for the study/program

o Help create scope scenarios and negotiate outcomes with study teams while taking into account the cost and value of scenarios

o Facilitate/assimilate integration of disparate data sources into datasets for decision making

o Utilize therapeutic knowledge and possess a deep understanding of the technology used to review data to ensure database deliverables are consistent and accurate

o Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to data deliverables

Process Improvement

o Continually seek and implement means of improving processes to reduce cycle time and decrease work effort

o Represent data sciences’ processes in multi-functional initiatives.

o Actively engage in shared learning across the Data and Analytics organization.

Work with partners to increase vendor/partner efficiencies

Basic Requirements:

Health Sciences Bachelor´s Degree plus 2 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, epidemiology etc...)

Excellent English (C1/Advance)

Additional Skills/Preferences:

· Demonstrated ability to effectively partner/influence a remote team and drive a technical project to deliver results

· Demonstrated ability to lead development of creative data solutions to address clinical development challenges

· Utilization of clinical/drug development knowledge and an ability to collaborate closely effectively with study team members (i.e. Statistics, PK, Operations, Medical)

· Ability to balance multiple activities, prioritize and manage ambiguity

· Demonstrated exemplary teamwork/interpersonal skills

· Demonstrated problem solving, attention to detail and result oriented behaviors in a fast-paced environment.

· Understanding of Post commercialization research (Observational studies)

Additional Information:

International travel may be required

Position location- Alcobendas (Madrid)

Eli 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 ( LillyRecruitingCompliance@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 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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