Location: Philadelphia Metropolitan Area
Therapeutic Expertise: HIV/Infectious Disease or Cardiovascular
Responsible for assigned data handling, review and management activities in support of clinical research studies. Implementation of Study Specific procedures compliant with Regulatory and internal SOPS, procedures and requirements. Responsible for the execution of data management plans for the design, and implementation of clinical data collection, review, clarification and reporting systems for clinical studies. Coordination of multiple data sources and the interaction with their stakeholders both internal and external. Manage within regulatory guidelines. Support the management of assigned project timelines and prioritization of tasks.
Qualifications: 3 years of relevant pharmaceutical and data management experience; competent with diverse CDMS platforms with extensive experience with EDC-based studies; data dictionaries MedDRA and WHO Drug Dictionary. Excellent written and oral communication skills; possess interpersonal and project management skills; preferred medical training; 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." 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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