Regional Clinical Research Associate

 

Spectrum Pharmaceutical Research Corp, a Texas based CRO, is growing and needing experienced Regional Clinical Research Associates (CRAs) to conduct on site monitoring of clinical trial data.

 

Responsibilities include monitoring (pre-study, initiation, interim and close-out visits) at investigator sites for GCP compliance and review/collection of clinical data, resolution of queries of CRF data with study site personnel, and file reports (visit and expense) in a timely manner.  Must comply with company and Sponsor SOPs and policies.

 

Requires a Bachelor's degree in Biology, Chemistry or Nursing.

Requires a minimum of 2 years CRA monitoring experience with a CRO or pharmaceutical company.  Must have expert knowledge of FDA guidelines and GCP as well as good computer, organizational, time management and problem solving skills.

 

Requires travel up to 80% of the time.

 

This is a regional, home based position.  Interested in candidates located in Northeast and Southeast U.S.  Eligible applicants must have home office and live within 25 miles of major airport.

 

Spectrum offers full benefits, paid time off, 401k, disability, 125 flex plan and the opportunity to work on cutting edge pharmaceutical and biotechnology projects.  Salary commensurate with experience.

 

For immediate consideration, please email or fax your resume with salary history to:  ryoung@spectrumcro.com or fax 210.377.4275.  EOE