You will play a critical role in leading and coordinating various clinical activities, working closely with physicians, subject matter experts, and a diverse set of stakeholders
Job Summary
You will play a critical role in leading and coordinating various clinical activities, working closely with physicians, subject matter experts, and a diverse set of stakeholders.
Key responsibilities include leading the process for drafting clinical synopsis, contributing to study design, and managing timelines to ensure high-quality deliverables.
IQVIA is committed to integrity in its hiring process and fosters a culture of belonging by valuing the perspectives of all talented employees worldwide.
Matching Summary
You will play a critical role in leading and coordinating various clinical activities, working closely with physicians, subject matter experts, and a diverse set of stakeholders.
Skills & Requirements
Must-have
clinical study design
clinical documentation drafting
regulatory submission review
stakeholder coordination
timeline management
Nice-to-have
diversity and inclusion
intelligent connections
smarter healthcare
patient outcomes
Key Requirements
Life Science PhD or MD (or equivalent)
Minimum 5 years of relevant clinical research experience
2+ years experience drafting clinical study synopsis
2+ years experience drafting clinical sections of key regulatory documents
Experience in drug development or pharmaceutical environment
Familiarity with regulatory and sponsor interactions
Demonstrated ability to design and implement complex clinical protocols