This role is responsible for ensuring end‑end execution of clinical trials in alignment with ICH-GCP, regulatory requirements, and company SOPs
Job Summary
This role is responsible for ensuring end‑end execution of clinical trials in alignment with ICH-GCP, regulatory requirements, and company SOPs.
You will collaborate extensively with cross-functional partners, global teams, clinical sites, and external vendors to ensure high-quality study execution, on time and within budget.
Key Responsibilities include leading and managing all operational aspects of assigned clinical studies, developing and maintaining essential study documents, and owning key study deliverables.
Matching Summary
This role is responsible for ensuring end‑end execution of clinical trials in alignment with ICH-GCP, regulatory requirements, and company SOPs.
Skills & Requirements
Must-have
ICH-GCP and global clinical research regulations
Manage investigational product accountability
Oversee CROs and vendors
Negotiate and manage CTAs and study budgets
Drive patient recruitment and timely study completion
Nice-to-have
Knowledge of local regulatory pathways
Work effectively in agile team environments
Hands-on approach with exceptional organizational skills
Key Requirements
Minimum 5 years of clinical trial management experience
Bachelor’s degree (or higher) in a scientific or related discipline
Experience managing multi-center and international clinical studies (preferred)