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Job #02559

About our client Our client is the proprietary pharmaceuticals division of an integrated global biopharmaceutical company. Their focus is to challenge the current standards and develop the next-generation therapies that revolutionize the treatment of cancer. Position Location Clinical Research Associate/Senior Clinical Research Associate Research Triangle Park, North Carolina Salary Highly competitive package, commensurate with experience Responsibilities 1) Monitor one or more clinical trials 2) Conduct pre-investigational site visits 3) Organize and participate in investigator meetings 4) Assist in clinical site contract, budget development and negotiation 5) Participate in managing distribution, collection and tracking of regulatory documentation to ensure site and sponsor compliance and audit readiness 6) Assist in query resolution 7) Participate in coordinating preparation of training materials for site initiation, contract monitor training and mentoring of new clinical team members 8) Identify and gather missing or incomplete data from clinical sites 9) Assist in planning, implementation, monitoring and management of clinical studies and maintaining the department’s central files Requirements 1) Bachelor’s degree in Life Science 2) Oncology experience (1 year of working with an oncology trial as a monitor) 3) 2+ years of experience as a Clinical Research Associate 4) Experience in GCPs 5) Good understanding of GCPs and regulatory documents 6) Exceptional communication skills 7) Willingness to travel – up to 70% (on a weekly basis)