Location: Florida (Southeast)
Therapeutic Expertise: HIV/Infectious Disease or Cardiovascular Medical Device
Participate in the site management and monitoring clinical trials. Ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. Familiar with a variety of the GCP concepts, practices, and procedures. Relies on experience and judgment to plan and accomplish goals. A wide degree of creativity and independence expected.
Qualifications: 5 years of relevant pharmaceutical and clinical research experience; requires medical training as a RN or NP; preferred medical degree with a BSN, MSN, DNP degree; must be highly literate and comfortable with the Internet, EDC systems, and MS Office applications; certification by ACRP or SOCRA desired; must be willing to travel up to 70% within region. Must be willing to undergo a Professional, Academic, Financial and Criminal background check.
Compensation: Full-time, Permanent, Salaried, Competitive Salary and Benefits
Please submit resume, references and salary requirements.
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