Regulatory Affairs Specialist

Tampa medical research company is seeking a Regulatory Affairs Specialist to process and implement plans and tools to support the regulatory compliance of clinical trials according to company standard operating procedures. Must have knowledge of federal regulations relating to clinical trials and good clinical practice. Bachelors’ degree plus 2 years’ experience with IND/IDE clinical trials required. 5+ years’ experience in clinical research and regulatory field preferred. ACRP and SoCRA certifications preferred. FT with benefits.

Submit resume electronically to EOE M/F/V/D/DFWP