Legal Administrator opportunity for someone who really enjoys a support role within a legal setting or a perfect, first step to gain experience at the start of a legal career. If you have a passion for
Responsibilities (a) Site management • Study site selection, initiation (SIV) and clinical monitoring. • Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources
Location: United Kingdom – Fully Remote Employment Type: Full-time Industry: Clinical Research / CRO / Pharmaceutical The Opportunity We are supporting a well-established, international Contract Research Organisation (CRO) in the search for an experienced Clinical Data
We are looking for experienced Freelance Medical Writers to support an immediate requirement with a leading international organisation working within the life sciences industry. This opportunity would suit an experienced clinical/regulatory writer who has current availability
Senior Clinical Data Manager | Global CRO | Home Based | UK | Permanent A leading global CRO is seeking an experienced Senior Clinical Data Manager to join its growing clinical data management team. This fully