Senior Clinical Research Associate

ProTrials Research, Inc.(1 month ago)

HybridFull TimeSenior$155,324 - $207,624 (estimated)Clinical Operations

About this role

The Senior Clinical Research Associate at ProTrials is responsible for overseeing and managing clinical trial site activities to ensure studies are conducted in compliance with protocols, SOPs, ICH GCP, and regulatory requirements. This role involves significant travel to clinical sites, working closely with investigators and site staff throughout all phases of the study lifecycle. The Sr. CRA also serves as a resource to project team members, supporting junior CRAs and contributing to high-quality data collection. The position sits within a women-owned, WBENC-certified CRO focused on ethical and impactful clinical research across pharmaceutical, biotech, and medical device sectors.

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Required Skills

Clinical Monitoring
Site Management
Site Training
Source Documentation
CRF Completion
Supply Management
Inventory Reconciliation
Sample Management
Safety Reporting
Data Review

+15 more

Qualifications

RN
Bachelor in Biological Sciences
Advanced Degree in Biological Sciences

About ProTrials Research, Inc.

protrials.com

ProTrials Research, Inc. is a woman‑owned, full‑service clinical research organization serving medical device & diagnostics and pharmaceutical & biotechnology companies. They deliver end‑to‑end clinical development support including clinical operations, site management, project management, and other supportive development services. Branded as "Experienced Professionals, Trusted Partners Worldwide," ProTrials emphasizes hands‑on trial management and site oversight across studies and geographies. Sponsors engage them for tailored CRO solutions and operational expertise throughout the clinical trial lifecycle.