Regional Clinical Research Associate

We have a need for a Contract Regional Monitor/CRA that's is located in either Denver, CO, Phoenix, AZ, Southern California (L.A or San Diego) or Central Texas (Dallas, Austin, San Antonio).
 
Therapeutic Area:  Pharmacology, Phase 1, Diabetes, Oncology, HIV
 
 
Specific experience: 5-7 years minimum regional monitoring experience in Phase I through IV studies. This candidate will be based in their home office and will be required to travel up to 60% of the time to monitor Phase I through IV studies.
 
The person in this position will be a fully independent home based monitor who is responsible/accountable in Pharma Development Operations for the identification, selection, set-up, monitoring and close down of investigational trial sites in one or more programs.  This person will be completely accountable for the site management and data quality of each site for which they are responsible.  They must be able to operate a home based office and be fully functional as a home based monitor.  This would include generating correspondence and reports without administrative help, making one's own travel arrangements, general clerical duties associated with managing a home based office and the ability to anticipate, trouble shoot and resolve various types of problems and issues independently and without peer support.  This person will also be expected to develop a rapport with potential investigators, representing many different medical specialties to facilitate the placement of future research studies at institutions and medical centers.