Senior Project Manager

该职位来源于猎聘 The Role

• Acts as our clients 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. Oversee and handle the completion of the Clinical Laboratory Worksheet.
• Enter protocol parameter information into PACS//ICOLIMS and other systems for new and/or amended protocols. Preparing QC materials.
• Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by crafting and updating the study specific Communication and Escalation Plan. Ensure adherence to the protocol specific monitoring plan. Maintaining study files and ensuring that all appropriate documents are properly maintained. Ensure that all necessary documents are archived at study closure.
• Provide Sponsors with study management reports.
• Dedicatedly monitor study budget.
• Set the timelines for 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 Defences or Initiations.
• Develop new tools, train new employees
• Performs additional relevant responsibilities as requested by management. What you need
• 3-5 years’ work experience within a central laboratory environment OR extensive clinical laboratory experience.
• Have a Degree in a Life Sciences or related discipline.
• Customer focussed with the ability to build excellent rapport with business partners.
• Excellent knowledge of Excel and PowerPoint.
• Comfortable with presenting to groups.
• Experience in attending Bid Defences.
• Super organised and remains calm in taking care of multiple priorities and working to tight deadlines.
• Passionate about developing a career within Project Management.