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Location: Philadelphia Metropolitan Area
Therapeutic Expertise: HIV/Infectious Disease or Cardiovascular
Manages clinical trials in humans including participation in the preparation of protocols, preparation of informed consent forms and case report forms, development and management of monitoring plans, administration of study budgets, project management of clinical services suppliers and Contract Clinical Research Associates (CRAs), as applicable, and management of project timelines and deliverables.
Qualifications: 3 to 5 years of relevant pharmaceutical and clinical project management experience; excellent written and oral communication skills; possess interpersonal and project management skills; preferred medical training as a LPN, RN or NP; preferred scientific degree with a BS and or MS degree; must be highly literate and comfortable with the Internet, EDC systems, and MS Office applications; must be "hands-on" and "doer;" ability to manage multiple tasks; demonstrated strong ability to work successfully in a team environment requiring matrix management skills; knowledgeable in all aspects of the Federal (FDA) regulations and requirements governing the conduct of clinical trials including, but not limited to, GCP and ICH requirements; demonstrated ability to make effective presentations in public settings; PMI certification 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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