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SR. Clinical Research Associate OncologyPharmaceutical Associates - Ridgefield Park, NJThe incumbent will be responsible for monitoring Phase I studies as necessary, and assisting in the management of a Phase III global study, including but not limited to interfacing with the CRO. Other responsibilities include: Reviewing Regulatory documents Reviewing and commenting on Scope of Work and proposals from all vendors Reviewing and commenting on Protocols, CRFs, and other study related documents assuring quality and consistency Tracking documents and work flow, participation in team, study, and vendor meetings as required Travel approximately 25-30% The incumbent will be responsible for monitoring Phase I studies as necessary, and assisting in the management of a Phase III global study, including but not limited to interfacing with the CRO. Other responsibilities include: Reviewing...originally from Pharmaceutical Associates,LLC - More Tools...
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