Job expirat
- Conducts trials in accordance with protocols, SOPs, local regulations and ICH-GCP guidelines, including feasibility, sites selections, obtaining necessary approvals and documentation, site initiations, monitoring and SDV, management of site recruitment performance, trial supplies management, data cleaning activities, close-out and archiving.
- Meets all local and company requirements with respect to safety reporting in trials
- Prepares necessary study documentation based on requirements
- Executes good quality data from Sites Staff
-Ensures timely and good quality data in all the required systems.
-University degree (medical doctor or pharmacist)
-Good command of English
-Documented current ICH GCP knowledge
-2-3 year experience as CRA in pharma industry or within a CRO
-Technical and professional knowledge
-Driving licence; availability to travel 50-70% of time
-Computer literacy.
Founded in 1982, Grafton Recruitment has established itself as a world class provider of recruitment solutions. Grafton has experienced an impressive growth pattern in the last five years. The network has built to a total of 70 branch operations spanning 19 different countries including the United Kingdom, Republic of Ireland, Chile, Czech Republic, Slovakia, Hungary, Poland, Lithuania, Russia, Portugal, France, Austria, Belgium, Turkey, UAE and Romania.