Precision for Medicine
Argentina
Responsible for delivery, in terms of timeliness and quality, of site activation readiness within the assigned country/sites and foreseeing and mitigating any risks; Preparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial and…
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View the original ad ↗Precision for Medicine · Slovakia
The primary focus of this role is global clinical trial budget template development. You will be responsible for translating complex clinical trial protocols and study documentation into accurate, comprehensive, and negotiation-ready global/site budget templates across multiple…
Precision for Medicine · Houston, Texas, United States
The Principal Study Manager will act as the person responsible to lead and direct scientific work to support analysis of assays for non-regulated, GLP-regulated, GCLP-regulated and commercial diagnostic (CAP / CLIA) regulated studies across all scientific teams supporting…
Precision for Medicine · Frederick, Maryland, United States
The Associate Director, Study Management will work effectively across multiple scientific teams to direct the delivery of study milestones within cost, time, and quality requirements. Strategically leads both indirect and direct reports, as well as external partners,…
Precision for Medicine · United Kingdom
Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.