The Senior Contract CRA will monitor clinical trials, either at the site or remotely, to ensure the studies are conducted in accordance with the protocol, SOP’s, ICH-GCP and all applicable regulatory requirements. You will be deployed to our client, a large CRO with a strong therapeutic expertise in oncology & immuno-oncology, on a contractual basis.

Experience requirements include, but are not limited to:

• 5+ years of monitoring experience

• Ability and willingness to travel

• Demonstrated and extensive Oncology monitoring

• Immuno-Oncology experience preferred

• Knowledge of ICH and local regulatory authority regulations relative to drug trials