Manager/Sr. Manager, Clinical Data Management

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.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

Purpose:

The Clinical Data Associate is accountable for the end-to-end clinical data sciences delivery for a clinical study, including clinical database build, data acquisition, storage, retrieval, and exchange. This role requires in-depth understanding of the clinical study design, data standards, study protocol, data flow, systems, and processes for collecting and managing clinical study data. The Clinical Data Associate is required to represent the clinical data sciences function and collaborate with and manage key study stakeholders in achieving study milestones and deliverables. The role is responsible for providing clinical data science leadership and ownership for a particular clinical study, set of studies, or programs.

Primary Responsibilities:

This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.

Clinical Data Science Delivery

• Execute project monitoring and quality oversight of sourcing providers for end-to-end data management activities from study set-up to trial execution through database lock delivery.
• Ensure vendor performance for the program-level flow of data, including across niche vendors and niche data sources (pharmacokinetics, immunogenicity, biomarkers).
• Partner with the Clinical Data Strategist in ensuring data flow design and data collection meet the requirements of the study protocol.
• Develop the Data Management Plan (DMP) and maintain the DMP throughout the lifecycle of the clinical study while ensuring that the DMP is followed in accordance with the study design and study protocol requirements.

• Drive data cleaning activities throughout study execution. Utilize therapeutic knowledge and possess a deep understanding of the technologies used to review data to ensure database deliverables are consistent and accurate.

• Help identify and drive implementation of post-production changes to the Clinical Database.
• Develop and maintain plans for key study deliverables (i.e., Data Quality Delivery Plan, Datalock Plan, Project Plan).
• Provide consultation and a high level of expertise in data management processes, principles, and deliverables to support clinical studies.
• Represent clinical data sciences in inspections and support inspection readiness efforts within the clinical data sciences function and cross-functionally.
• Effectively apply knowledge of applicable internal, external, and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to data deliverables.
• Manage and drive requests for copyrights and translations for study-related documents.
• Drive build implementation for eCOA, ensure execution of eCOA deliverables (on time with high quality), and serve as eCOA primary point of contact (POC).

Project Management

• Ensure that the clinical data science deliverables meet scope, cost, and time objectives.
• Manage study timelines for clinical data deliverables (FPV to database lock)
• Drive the planning, readiness, coordination and communication of activities leading to database lock
• Coordinate/lead data management milestones for data transfers and database locks.
• Manage scope of the deliverables through scenario planning and negotiating desired outcomes with study teams while taking into account the cost and value of scenarios.
• Practice effective risk management to mitigate or manage risks to study deliverables.

Communication

• Act 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 Improvement

• Continually seek and implement opportunities for process improvements, automation to drive efficiencies, reduction of cycle times, and improvements in quality.
• Represent clinical data sciences’ processes in cross-functional initiatives.
• Actively participate in shared learning across the Data and Analytics organization.
• Work with partners to increase vendor/partner efficiencies.
• Prepare recommendations for new or improved processes relating to clinical data management. 

Minimum Qualification Requirements:

• Master’s degree in a scientific or technical field such as Informatics/Analytics, Life Sciences, Statistics, Information Technology, Epidemiology, Computer Sciences (or Bachelor’s degree plus 5 or more years of experience in clinical data management or areas that closely intersect with clinical data management, such as statistics, data analytics, information technology, health outcomes, etc...)

Other Information/Additional Preferences:

• Demonstrated ability to effectively partner/influence a virtual team and drive a technical project to deliver positive results
• Proven ability to lead development of creative solutions to address data-related clinical development challenges
• Passionate about improving technological solutions using new technologies
• Society of Clinical Data Management certification
• Working 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 participant to analysis and applying this knowledge to data solutions
  • Utilization of clinical/drug development knowledge and an ability to liaise effectively with study team members (i.e., Statistics, PK, Operations, Medical)
  • Strong therapeutic/scientific knowledge in the field of research
• Knowledge of medical terminology
• Domestic and international travel may be required

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 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.

Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.

Full-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.

#WeAreLilly