Job Role- Clinical Project Lead III
Employment Type-1-year contract
Pay rate-$60-70/hr
Location-Bridgewater, NJ
Description:
• Accountable of the customization and regular update of the activities/work packages under his/her perimeter
• Ensure the project strategy is reflected in terms of Planning into the operational plan in the customization horizon in consistency with resources and costs aspects
• Play an OPCM Leader role for the clinical studies, coordinating activities from Clinical Supply and TMED (CSD and PK) OPCM teams (Operational impact management and PPM interface )
• Analyze the project deliverable timelines and critical path activities
• Communicates planning information across the Clinical Sciences & Operations platform and to any key IPOM OPCM interfaces or Regulatory OPM as needed
• Identifies and anticipates any deviations, alerts key IPOM OPCM interfaces or Regulatory OPM in case of major events having an impact on project milestones and propose recommendations / facilitate decision making
• Provide reporting and analysis to support the project team and operational teams, including during project meetings
• Ensure a dedicated communication with the Capacity Management team within CSO OPCM group and Clinical Trial Finance (CTF) team in Finance.
• Ensure history data follow-up in the planning tool and coordinate quality controls of planning data
• Once agreed with Project actors, CSO OPCM is the single accountable person for the accuracy of the plan entered, its customization in the planning tool.
• Ensure the project strategy is reflected in terms of Planning into the operational plan in the customization horizon in consistency with resources and costs aspects
• Play an OPCM Leader role for the clinical studies, coordinating activities from Clinical Supply and TMED (CSD and PK) OPCM teams (Operational impact management and PPM interface )
• Analyze the project deliverable timelines and critical path activities
• Communicates planning information across the Clinical Sciences & Operations platform and to any key IPOM OPCM interfaces or Regulatory OPM as needed
• Identifies and anticipates any deviations, alerts key IPOM OPCM interfaces or Regulatory OPM in case of major events having an impact on project milestones and propose recommendations / facilitate decision making
• Provide reporting and analysis to support the project team and operational teams, including during project meetings
• Ensure a dedicated communication with the Capacity Management team within CSO OPCM group and Clinical Trial Finance (CTF) team in Finance.
• Ensure history data follow-up in the planning tool and coordinate quality controls of planning data
• Once agreed with Project actors, CSO OPCM is the single accountable person for the accuracy of the plan entered, its customization in the planning tool.