Tigermed is seeking a Clinical Research Associate to manage study sites, conduct SIVs, and monitor trial progress in line with protocol and regulatory requirements. You will train site staff on ICH-GCP and ensure accurate documentation throughout the trial lifecycle.
Responsibilities include safety reporting, finance administration, and maintaining study tools and systems, with a focus on quality and regulatory compliance across study sites.
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Senior Clinical Research Associate (UK Contractor) employer: Tigermed
As a fully remote employer in the pharmaceutical industry, we pride ourselves on fostering a collaborative and inclusive work culture that values communication and teamwork. Our employees benefit from extensive growth opportunities, including the chance to lead and establish teams within a global framework, all while enjoying the flexibility of remote work. Join us to be part of a dynamic environment where your expertise is valued and your contributions make a meaningful impact.
