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Clinical data management (CDM) involves collecting, organizing, and verifying clinical trial data to ensure accuracy, integrity, and compliance. CDM plays a critical role in supporting trial outcomes, protecting patient safety, and meeting regulatory requirements. It covers everything from case report form (CRF) design to database lock and data submission.
CDM in clinical research can be delivered by full-service CROs or through Functional Service Provider (FSP) models that allow clients to outsource select tasks. At GForce Life Sciences, we offer flexible clinical data management services that support both models, giving clients the ability to scale resources as needed.
Our clinical data management consultants provide tailored support across therapeutic areas and study phases. We offer expertise in clinical trial data handling, from start-up to closeout, using advanced tools and processes that align with sponsor systems. Whether you need biotech or pharmaceutical data management, our team helps ensure consistency, clarity, and regulatory alignment throughout.