Clinical Project Manager
Pharmaron

The Clinical Project Manager (CPM) will be responsible for the overall direction, implementation, coordination, control and execution of global-scale clinical projects. Additionally, you will support at the project planning phase, along with ensuring that key milestones throughout the plan are completed on time, to a high quality and within required standards.

Essential Responsibilities Include:

• Serve as client advocate and primary point of contact for client, functional leads, and vendors on assigned studies
• Organizes and leads meetings as appropriate
• Evaluate and Initiate the Project
• Develop project-related plans and trial-related forms, including but not limited to: project management plan, clinical monitoring plan, risk management plan, communication plan, recruitment plan, document management plan, and quality management plan.
• monitor and control the schedule of the entire project to ensure that the trial is carried out according to the plans. Ensure that the project is completed in accordance with the budget, schedule and contract specifications.
• Ensure clinical operations and procedures comply with the requirements of the protocol, SOP, ICH-GCP/China GCP and relevant laws and regulations, and timely report safety events and related deviations according to the time limits of the protocol and laws and regulations.
• calculate and apply investigational products at the project level, and ensure that the packaging and quantity of investigational products meet the requirements of the trial.
• Plan and conduct the investigator meeting, and ensure that the investigator meeting will achieve the desired results.
• Collaborate with the Data Manager, the CRFs are reviewed and developed in accordance with the trial protocol. Ensure that the CRFs are available at the trial site prior to FPFV.
• Review meeting minutes, internal and external correspondence, and all project-related reports.
• prepare project briefings and send them to the Sponsor on time as agreed.
• Support organizational growth and development

• BS/BA Degree (or equivalent) in relative field with 5+ years of relative experience
• Or MS Degree (or equivalent) in relative field with 3+ years of relative experience
• Candidate should have experience in clinical studies, preferrable in Oncology
• Minimum of 3 years as a successful Clinical Project Manager at a CRO preferred