Provide centralized, global clinical trial oversight within our Functional Service Provider (FSP) model
Lead Study Management Teams (SMTs)
Oversee country and site-facing activities
Ensure trials are conducted with the highest standards of quality, compliance, and inspection readiness—from start-up through close-out
Drive trial delivery across the full lifecycle: feasibility, site selection, start-up, execution, and close-out
Act as the central subject matter expert for assigned protocols
Provide oversight of CROs and global vendors supporting site-facing activities
Ensure continuous inspection readiness in accordance with ICH-GCP, applicable regulations, and sponsor SOPs
Lead feasibility activities and provide data-driven recommendations
Oversee trial documentation, filing, archiving, and retention
Lead teams across projects or programs and provide coaching and mentoring to less experienced team members.

Bachelor’s degree (or equivalent) in Life Sciences (e.g., Biology, Chemistry, Nursing, Pharmacy)
6+ years of clinical trial management experience in pharma and/or CRO environments
8+ years of clinical trial management experience, including leadership of complex global studies
Proven experience managing trials from start-up through database lock and close-out
Experience coordinating global, virtual teams in a large matrix environment for 2–3+ years
Therapeutic area experience required
Deep knowledge of ICH-GCP, regulatory requirements, and clinical operations best practices
Strong project management, planning, and risk mitigation skills
Demonstrated ability to manage country and vendor budgets, including OOPs and cost drivers
Experience with CTMS, TMF systems, and Microsoft applications
Monitoring experience preferred (or equivalent central monitoring/data management experience)
Strong analytical, decision-making, and communication skills
Fluent in English; local language proficiency as required
Willingness to travel as needed.

Trial Delivery Manager, Multi TA

Key skills