... writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and ... acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant ...

... and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research ...

... academic / vocational qualification. Minimal clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1-2 years) in a clinical environment ...

... (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management ... nursing field. • With 2-3 years of experience within the clinical research industry ...