The Clinical Trial Project Management Assistant (CTPMA) provides technical and project administrative support to the Clinical Trial Project Managers (CTPM) and…

Scientific data and information are core assets of Lilly. The purpose of the Scientific Communications Associate - Regulatory role is to work with cross…

The purpose of the The Associate, GRA-NA, is accountable for the operational and technical registration management processes that support the expedited delivery…

The Clinical Data Management Analyst is responsible for trial level clinical data execution. The Clinical Data Management Analyst will collaborate with the…

Demonstrate in-depth understanding of format and style requirements for labeling documents including regulations and trends. Review or QC work of others.

Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community,…

Global Medical Information (GMI) plays an integral role in driving medical launch strategy through creation of answers to unsolicited requests from customers …

The Clinical Trial Project Manager (CTPM) Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable…

In an age of targeted multi-channel experiences, the volume of content and speed to bring tactics to customers is dramatically increasing and we are responding…

Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community,…

Brand and marketing teams rely on strong market research support to understand brand performance, identify new opportunities, create marketing plans, and…

The CMC Regulatory Specialist has the responsibility to support new product approvals, existing product renewals, and post-approval changes for global…

The role will be based at LCCI in India. Review and approve promotional and non-promotional materials across different therapeutic areas and brands in Veeva…

Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community,…

The primary focus of the TMR is to review and approve UK affiliate materials across different therapeutic areas and brands from a technical medical point of…

The purpose of the LCCI Editor role is to partner with brands, agencies and internal partners to ensure quality, speed, value and compliance throughout the…

The primary responsibility of the Execution Lead is to execute the responsibilities related to track and withdrawal and inventory management processes as…

The Clinical Data Management Associate is responsible for trial level clinical data execution including database structure, content and meaning, acquisition,…

The purpose of the Manager; Economic Modelling role is to work with cross-functional, multidisciplinary teams to develop Health Technology Assessment (HTA)…

To solve the complex problems of a global business and the ever-evolving data and analytics landscape, the organization generally requires advanced degrees in…