Manage all clinical aspects of complex Oncology Phase I-IV studies, reviewing clinical trial budgets, Sponsor identification, and contracting and project management. Managing site agreements, ensuring that change orders and budgets meet specifications, ensure all clinical trials are executed in compliance with ICH & GCP guidelines/regulations and Sops, assist with the writing and development of SOPs, thoroughly review Clinical data in Medidata RAVE,INFORM, IBM Clinical Development, Trial Master, Protocol First and Perspective my Trials databases, use IRT systems such as Almac, Suvoda, Cenduit and Clinphone and submit Initial & Annual reports, AE/SAE to sponsors and Institutional Review Board (IRB). Masters in Pharmaceutical Industry or related. Please email resumes to

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