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

Job #02689

About our client Our client is a rapidly growing, global CRO, headquartered on the East Coast. The company has managed close to 150 protocols, boasts a deep network of over 3000 sites and has developed unparalleled expertise in cardiology and device studies. With strong financials, an experienced management team and loyal customer base, this is a strong opportunity for someone that wants to put their drive and initiative to work! Position Location Clinical Project Manager Rockville, Maryland Salary Highly competitive package, commensurate with experience Responsibilities 1) Provide project-specific support as a primary contact for project coordinators, CRAs, internal key clinical personnel and investigational site personnel 2) Train CRAs in project-specific areas and in administering the conduct of trials 3) Monitor status of projects 4) Track reporting and follow up on serious adverse events 5) Monitor on-site study progress and contribute to writing of study summary reports for agency/sponsor submission 6) Perform all duties of CRAs (as required) Requirements 1) Bachelor’s degree in a scientific discipline 2) 4+ years of clinical trial experience in the pharmaceutical or bio-tech industry, including both site management and project management 3) Excellent knowledge of FDA regulations and GCPs 4) In-depth knowledge of current federal regulations and guidelines 5) Excellent interpersonal and communication (written and spoken) skills 6) Superb leadership skills 7) Ability to set/meet personal short/long-term goals to complete assignments 8) Ability to anticipate problems relating to projects and develop/implement solutions 9) Willingness to travel – up to 20%