Lilly is seeking an Associate Director – Data Standards to join their team in Indianapolis, IN. The role involves providing technical leadership and ownership for data standards across the clinical trial dataflow.
About the Role
As an Associate Director – Data Standards, you will be responsible for developing and maintaining standards for clinical trial data, ensuring data transfer between Lilly and external partners, and developing metadata to automate the clinical trial dataflow process. You will collaborate with Statistics colleagues to ensure compliance with industry data standards, engage with external data standards organizations, and seek process improvements to enhance efficiency.
About You
Required:
Master’s degree in Medical Informatics, Information Technology, or Statistics, or a bachelor’s degree with 5 years’ experience in clinical data management, data standards, IT, or statistics.
Legal authorization to be employed in the United States.
Preferred:
Strong interpersonal and leadership skills.
Excellent oral and written communication skills.
Project management skills.
Familiarity with SQL, ORACLE, XML.
Knowledge of medical terminology.
Vendor management/oversight skills.
Willingness to travel domestically and internationally.
Benefits
Company bonus eligibility based on performance.
Comprehensive benefits package including medical, dental, vision, and prescription drug benefits.
401(k) and pension plans.
Vacation benefits.
Flexible benefits such as healthcare and dependent day care flexible spending accounts.
Life insurance and death benefits.
Employee assistance program, fitness benefits, and employee clubs and activities.
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