Qualifications:
A 4 year college degree is required, preferably in a Life Science or related field. A BSN, BA, or BS degree is acceptable.
A minimum of 2 years experience as a Clinical Research Associate/Monitor is required, 3+ years experience preferred.
Good computer skills are necessary (Microsoft Office, EDC, web-based communication tools, clinical trial management software).
A solid knowledge of FDA clinical trial regulations and ICH GCP guidelines is necessary.
Individual must demonstrate the ability to work independently and on a multidisciplinary team. Strong inter-personal skills, and strong written and verbal communication is required.

Our company website:
rpsweb/
RPS, a top 10 global CRO growing 35% every year, provides comprehensive global Phase I-IV clinical development solutions to the Pharmaceutical, Biotechnology, Medical Device and Diagnostic industries. By combining an experienced clinical research operations infrastructure with the industry's largest resourcing engines, RPS is uniquely positioned to offer our clients a broad spectrum of outsourcing solutions. These solutions range from globally integrated functional and cross-functional programs to enhanced global full service solutions, and are powered by highly experienced and seasoned project teams providing innovative, seamless, cost-effective and high quality services.
RPS provides comprehensive coverage across the Americas, Europe and Asia. Our global corporate headquarter is located in Pennsylvania, USA; Currently Asia offices are located in Beijing, Shanghai, and Seoul.

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