Tigermed seeks an experienced Clinical Research Associate to oversee site management, initiation visits, and regulatory compliance across UK sites. You will monitor trial progress, ensure data integrity, and coordinate training for site staff in line with ICH-GCP and sponsor requirements.
Responsibilities include study start-up, site initiation visits, safety reporting, document archiving, and collaboration with investigators to maintain study timelines and quality.
#J-18808-Ljbffr
Senior Clinical Research Associate – Site Management in Preston 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.
