TheClinical ResearchAssociate Sr (CRA SR) role is accountable forperformanceand compliance for assigned protocols and sites in a country.

Under the oversight of the CRAmanagerthe person ensures compliance of study conduct withICH/GCPand country regulations, our companypolicies and procedures, quality standards andadverse event reportingrequirements internally and externally. Acts as primary site contact and sitemanagerthroughout all phases of aclinical researchstudy, taking overall responsibility of allocated sites. Actively develops and expand the territory forclinical research, finding and developing new sites. Participates in internal meetings and workstreams as SME for monitoring processes and systems.

Responsibilities include, but are not limited to:

• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
• Performs c...