Tigermed is seeking an experienced Clinical Research Associate to manage study sites, initiate and monitor studies in accordance with protocol and regulatory requirements. You will coordinate safety reporting, budgeting and contract processes, and maintain essential study documentation across multiple sites.
The ideal candidate has a Bachelor degree in a medical-related field and at least 8 years of CRA experience, with strong knowledge of ICH-GCP and trial operations, plus proficiency in Word,
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Senior Contractor CRA – UK: Site & Safety Lead in Woking 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.
