Principal Investigator Contract

"At ICON, it's our People that set us Apart"

Are you interested in improving your knowledge of Clinical Trials and contributing to our culture of process improvement with a focus on streamlining our processes of adding value to our business and meeting client needs?

Contract Principal Investigator within ICON: Aid in recruiting and screening healthy volunteers and patients for Phase 1 clinical trials. To provide medical support for the conduct of studies. Responsible for the safety and welfare of volunteers and patients during studies. Provide medical input into study protocols, interim reports, safety reports and final study reports, assisting project management with the leadership of studies, and liaise with Sponsor companies from a medical perspective. Develop and maintain a high level of skill in designing, conducting, and interpreting clinical pharmacology studies. Maintain level of skills necessary for the practice of clinical medicine.

To succeed you will need:  Have a Medical Degree. Five plus years of Patient Care Experience. License to Practice Medicine in TX. Experience in Clinical Trials.

What’s Next?

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.