We are an EasyHiring recruiting company that is looking for candidates for our partners for the position of Head, Clinical Drug Development Standards in New Jersey - Princeton for work in Princeton - NJ.

The Head of Drug Development Standards is responsible for providing strategic and operational leadership to data and analysis standards, macro development and innovation within Global Biometrics and Data Sciences (GBDS), enabling delivery of end to end standards for drug development, driving efficiency in delivery across drug development and research portfolio.

Key Responsibilities

Establish and implement a dynamic organization focused on building / managing standards scientific content, CDISC aligned metadata, macros. Partnering cross-functionally, drive efficiency in end-to-end operations, driven by standards content. Utilize innovation experts to continue driving future focused solutions focused on standardization and automation.

Lead a cross-functional team of data collection and analysis experts within a global operating model. Develop and execute the strategy to deliver standards content and operational metadata management for drug development.

Partner with and influence other key functions of Drug Development, Translational Medicine and Medical to ensure visibility and oversight of standards utilization by establishing KPIs and impact of standards to the delivery of the portfolio.

Develop and drive standardization strategy in partnership with Data Management, Clinical Science, Biostatistics, Statistical Programming, Clinical Operations, etc. Build and execute on a roadmap and execution plan to create an industry-leading end-to-end standardization capability.

Transform the organization through development and implementation of a comprehensive Standards and Innovation strategy, streamline drug development processes and enhance operational efficiency.

Reinforce the commitment to leadership and development by providing or facilitating training and experiential opportunities and continuous coaching and feedback throughout the organization.

Qualifications & Experience

Advanced degree preferred; 12 years of relevant industry experience

Strong experience in Clinical Development Standards and well versed in industry trends in standardization, CDISC and automation.

Excellent knowledge and skills with the broad expertise in Clinical concepts and driving clinical standards

Relevant working experience in the pharmaceutical industry

Successful track record of working across complex, global organization.

Strong people leader with a mindset to grow Drug Development Standards & Innovation

Job Type: Full-time

Work Location: On the road