Job Summary

• This role is responsible for coordinating and implementing strategies to improve trial participant diversity across all regions and across all Therapeutic Areas.
• The PM DICT will lead the harmonization and standardization of DICT activities across different regions and functions while understanding and addressing the local priorities.
• This role will be instrumental in identifying external partnerships (vendors, patient groups, HCP groups) to ensure diversity of clinical trial participants.

Matching Summary

Skills & Requirements

Key Requirements

• 6+ years of experience in pharmaceutical industry
• Fluent English speaking and writing
• BS/MS/PhD/Equivalent background
• PMP certification (plus)

Work Rights