Lead the clinical elements of trials including site start-up, enrolment, and monitoring.
Deliver trial milestones on time while maintaining quality.
Regulatory documentation and ongoing oversight with cross-functional teams.
Mentor and train team members to build capabilities.
Identify timeline risks and propose actionable mitigation plans.
Lead CRAs to establish site relationships and quality oversight.

🎯 Requirements

Bachelor’s degree in science/health field or equivalent.
Experience leading multi-country clinical studies in CRO/Pharma/Biotech (clinical lead).
Knowledge of GCP/ICH guidelines and the clinical development process.
Willingness to travel domestically and internationally (overnight).
English language proficiency.
MS Office, MS Project; CTMS, eTMF, EDC, IXRS experience.

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