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Location: Philadelphia Metropolitan Area
Therapeutic Expertise:HIV/Infectious Disease, Cardiovascular and/or Adult Medicine.
Participate in the site management, coordination and monitoring clinical trials. Ensures compliance with protocol and overall clinical objectives. Demonstrated performance in subject/patient recruitment and retention. Knowledge of FDA regulatory requirements is required. Trained in GCP concepts, practices, and procedures. Relies on experience and judgment to plan and accomplish goals. A wide degree of creativity and independence.
Qualifications: 3 years of relevant pharmaceutical and clinical research management experience; requires medical training as a MA, RN or NP; preferred medical degree with a LPN, 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; certification by IATA a plus. 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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