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REGISTER YOUR INTEREST

Parexel are registering interest for Senior Clinical Research Associates for UK based sponsor dedicated roles. Experience in oncology trials and RECIST criteria is essential. A minimum of 4 years' experience in CRO or Pharma trials environments is also 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