We are looking for an organized, flexible clinical research associate to oversee clinical trials. To be successful in this role, you should be able to recognize ongoing problems and initiate appropriate solutions.

The ideal candidate will be detail-oriented, have the ability to multitask and be able to collaborate with various role players.

• Reading protocols - What’s supposed to happen

• Entering data from screening to drug dispensation

• Answering related queries

• Only employees can see the protocol

• Standard bread and butter clinical research

• Other tasks and responsibilities as needed.

• 2 to 3 years working with clinical trials - oncology

• Experience in early-phase research (phase 0, phase 1, and phase 2)

• Experience within EMR (potentially a requirement)

• Cancer clinical trials in the early phase