When our values align, there's no limit to what we can achieve.
 

Parexel are seeking sponsor dedicated Senior Clinical Research Associates, to be based in Belgium. Experience in oncology trials and RECIST criteria is essential.

The Senior CRA will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with the Study Monitoring Plan (SMP) and will be performed virtually for the majority of activities to supplement on site visit requirements. The Senior CRA will collaborate with the Site Manager to assure that the site complies with the protocol and is inspection ready and will coordinate with institutions and investigators at the local level.

Some specifics about this advertised role