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Job #02364

About our client Our client is a leading privately held pharmaceutical company with operations in over 40 countries. With marketed products, an experienced management team and an empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate. Position Location Senior Clinical Research Associate New Jersey Salary Highly competitive package, commensurate with experience Responsibilities 1) Participate in planning of study implementation with managers 2) Review protocols to become familiar with details and communicate with study personnel to confirm/clarify protocol guidelines 3) Participate in protocol development and CRF design 4) Use internal investigator lists and externally published sources to contact potential investigators 5) Travel to study sites to perform evaluation of eligibility and enlist investigators as appropriate 6) Discuss details of study budgets with investigators and ensure that contracts are properly executed before initiation of studies 7) Prepare and present protocol and study related presentations at investigator meetings 8) Travel to study sites on an ongoing basis to monitor progress 9) Collect, review and correct case report forms in accordance with study timelines 10) Monitor progress of enrollments and other benchmarks to assess ongoing progress Requirements 1) Bachelor’s degree in a scientific discipline 2) 6+ years of clinical trial experience in the pharmaceutical or biotech industry 3) 5 years of experience as a field monitor 4) Experience in monitoring clinical trials from qualification to closeout 5) Supervisory experience preferred 6) Strong knowledge and understanding of FDA Regulations and GCPs 7) Exceptional communication skills 8) Willingness to travel – up to 70%