Act as the sponsor's main contact person in all matters regarding our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department. Review newly assigned protocols and amendments. Coordinate and manage the completion of the Clinical Laboratory Worksheets (CLW) and communicate information as required to other departments within ICON Central Laboratories (and ICON Clinical CRO if appropriate). Enter protocol parameter information into PACS//ICOLIMS and other systems for new and/or amended protocols. Prepare and review clinical study specific materials. When possible, coordinate with other departments for the preparation of study specific materials. Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Maintain clinical study specific study files and ensure that all appropriate documents are properly maintained and filed. Monitor study progress throughout the study, using ICON tools and communicate pertinent information to clients/sponsors. Provide Sponsors with study management reports. Provide client with support on ICONLabs system. Inform team leader about study progress. Escalate issues of potential client/site dissatisfaction to appropriate management. Facilitate client satisfaction by acting as their main contact in all matters regarding ICON Central Laboratories' (ICL) services, including the setup and day-to-day management of studies; Provide clients with regular study updates and communicate study progress to them and PM Leadership in a responsible and professional manner. Proactively monitor study budgets and monitor the progress of shipment requests for storage samples and verify data. Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off Meeting Bid Defenses or Initiations. Provide training to other PMs as requested by management. Telecommuting is permitted. Domestic travel required 10% of the time.

Bachelor's degree in Biological Sciences or related field (or its foreign equivalent) plus 2 years of experience in the job offered or a related occupation. Must have 2 years of experience with laboratory methods and workflows; 1 year of experience implementing metrics and maintaining project timelines and budgets; and 1 year of project management experience, including scheduling and hosting meetings and organizing meeting agendas. Telecommuting is permitted. Domestic travel required 10% of the time.

Apply at www.jobpostingtoday.com Ref #28250.