Clinical Study Operations Engineering Program Manager - Health

Description

Minimum Qualifications

• B.S. degree in biomedical engineering or any engineering discipline, or equivalent
• 5+ years of direct experience in clinical project management, strategic partnerships, or clinical operations within Health or Technology
• Strong human research background with a comprehensive understanding of the end-to-end study lifecycle, GCP, and domestic/international regulations
• Proven track record of managing and onboarding global CROs and diverse external vendors
• Ability to knit together disparate sources of information into a strong strategic narrative and perform data analysis to drive measurable results
• Expert analytical and negotiation skills, adept at facilitating actions, resolving conflicts, and delivering crisp, effective communication to executive leadership
• Proven ability to project manage and oversee clinical data management activities, ensuring adequate resourcing, vendor compliance, and strict data integrity across the study lifecycle.
• Self starter and critical thinker with the ability to work autonomously, establish priorities, and thrive in a highly ambiguous, fast paced environment
• Superb communication skills including effective listening, clear and concise writing, and the ability to articulate complex project updates to executives
• Ability to be onsite; this role is a hybrid, in-person position
• Some travel is required, approximately 25%.

Preferred Qualifications

• Experience leveraging AI, digital platforms, or advanced analytics in clinical recruitment and study operations
• Direct experience strategizing and mapping clinical operations for OUS regions