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Job #03608

About our client Our client is a well-established international research organization with its own oncology division. They are currently looking to hire Contract CRAs in Los Angeles, Atlanta and Florida. Position Location Clinical Research Associate – Contract USA Salary Highly competitive package, commensurate with experience Responsibilities 1) Conduct site visits (initiation, monitoring, termination) 2) Ensure adherence to FDA and ICH-GCP regulations and local regulations 3) Evaluate and report site performance and protocol compliance 4) Instruct the site staff in their roles and responsibilities in conducting clinical trials 5) Monitor assigned clinical trials performed under the auspice of the company 6) Interact with all the different departments (Monitoring Resources, Project Management, Quality Assurance and Data Management Department) 7) Ensure the completion and collection of regulatory documents 8) Perform data verification of source documents, product accountability and supply tracking and CRFs collection 9) Ensure completion and collection of SAEs 10) Assist with data validation and resolution of queries 11) Ensure compliance with SOP Requirements 1) Scientific background (Research Nurse, Scientist, Pharmacist, BS, MS, Ph. D.) 2) 3+ years of experience in conducting site visits (initiation, monitoring and termination) with a strong oncology background. 3) Good interpersonal communication skills and sense of prioritization 4) Rigorous, organized, autonomous and self-motivated individual with ability to work in a multi-cultural environment 5) Good knowledge of computers (Word, Excel, PowerPoint) 6) Willingness to travel (60% non-regional travel with 10 monitoring days on-site per month)