Moretta R.

I am a clinical operations subject matter expert with extensive experience supporting complex biotech and pharmaceutical trial execution, with a focused specialization in eCOA (electronic Clinical Outcome Assessments) and decentralized clinical trials (DCT) strategy, governance, and implementation. Success depends on more than vendor selection. It requires operational alignment, governance oversight, workflow integration, regulatory awareness, and a clear understanding of the patient journey throughout the study lifecycle. I advise sponsors and biotech teams on building structured, defensible digital trial strategies that support execution, data integrity, regulatory readiness, and patient-centered study delivery. Core areas of expertise include: eCOA vendor evaluation and strategic selection Vendor governance and performance oversight Implementation strategy and workflow integration Cross-functional alignment (Clinical, Data, Regulatory) Operational risk assessment and mitigation My approach is structured, experience-based, and grounded in industry best practices. Available for advisory engagements, governance reviews, and strategic implementation planning.