Clinical Research Coordinator, Arizona

 Carla_Aragon@kellyscientific.com

Clinical Research Coordinator, Arizona

Great opportunity for Direct Hire opportunity to support onsite studies in Arizona East Valley Area. 

Summary:

Will assist Principal and Sub-Investigators.

Responsible for the successful coordination of clinical trials with strict adherence to the study protocol, guidelines, regulations, and policies.

Your responsibilities:

Support recruitment activities to meet enrollment targets.
Ensure each study subject is fully informed of the study details at the time of consent.
Collect study data, maintain accurate source documentation, and ensure Investigator review of all information for oversight of patient safety and quality data.
Communicate closely with monitors, sponsors, and Investigators.
Train staff who will be working on the study.
Scheduling of subjects for study related visits. For example, assure study subjects are scheduled with the doctor and any other procedures that might be required to complete that visit, such as pap smears, endometrial biopsies, mammograms, bone scans, etc.
Processing and shipment of laboratory specimens.
Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products.
Participate in web conferences and teleconferences for each study protocol to stay informed and updated.
Your opportunities:

Contribute to essential medical research to make a positive impact in the future of healthcare.
The work you do now can help millions of people live healthier lives in the future.