To apply for multiple jobs at once, please select the check box beside the desired jobs on the main job category page.

Job #02386

About our client Our client is a reputable, mid-size CRO that is experiencing unprecedented growth. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. Position Location Project Manager New Jersey Salary Highly competitive package, commensurate with experience Responsibilities 1) Provide project-specific support as primary contact for Project Coordinators, CRAs, internal key clinical personnel and investigational site personnel 2) Train CRAs in project-specific areas 3) Administer conduct of trials 4) Perform all responsibilities of CRAs 5) Track status of projects with support from logistics coordinators 6) Monitor on-site study progress and contributing to the writing of study summary reports for agency/sponsor submission 7) Track report and follow up on serious adverse events with support from logistics coordinators Requirements 1) Bachelor’s degree in a scientific discipline 2) 4+ years of clinical trial experience in the pharmaceutical or biotech industry, including both site management and project management 3) 3+ years of experience in field monitoring 4) 1+ years of clinical project management experience 5) Strong knowledge and understanding of FDA Regulations and GCPs 6) Thorough knowledge of current federal regulations and guidelines 7) Highly effective in setting/meeting personal short/long-term goals to complete assignments 8) Ability to anticipate problems relating to projects and develop/implement solutions 9) Solid leadership skills 10) Highly developed interpersonal written/oral communication skills 11) Willingness to travel – up to 20%