Biopharma Clinical Operations Expert
$130 per hourAlpheva
Evaluate clinical-trial planning, site operations, protocol execution, monitoring, and inspection-readiness decisions across drug-development programs. Review AI-generated recommendations for feasibility, patient safety, data integrity, protocol compliance, and sponsor or CRO oversight. Identify operational assumptions, missing documentation, escalation gaps, and site-management decisions that conflict with ICH-GCP practice. Provide clear corrections that reflect how experienced clinical-operations leaders balance timelines, quality, and participant protection. Remote, project-based contract work. Scope and hours depend on project matching; the listed hourly range applies to matched work. Requirements 8+ years in sponsor, CRO, or site-level clinical operations Deep knowledge of ICH-GCP, trial monitoring, site management, and protocol-deviation handling Clinical program leadership or inspection-readiness experience preferred Pay $130–$200/hr Alpheva is a new expert network (launched September 2026); payout methods are not published yet, so confirm your first payment before scaling up. #J-18808-Ljbffr Alpheva
Vacancy posted 4 days ago
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