Job Description

• *Recognize, exemplify and adhere to ICON's values which centre on our commitment to People, Clients and Performance.
• *As a Professional, the employee is expected to recognize the importance of, and create a culture of, process improvement with a focus on streamlining our processes, adding value to our business, and meeting client needs.
• Participate in opportunities for process improvement. Lead or participate in process improvement initiatives, as assigned, and promote the sharing of best practices.
• *Travel (approximately 25%) domestic and/or international.
• *Primary point of contact for the clinical aspects of designated projects and responsible for developing successful cross-functional relationships with internal and external stakeholders.
• *Responsible for planning, scheduling and implementing the clinical aspects of projects in line with contract and budget, e.g. implementation of protocol and amendments; protocol deviation prevention, tracking and reporting; IP management, timely investigator payments.
• *Responsible for driving enrolment as per contracted timelines.
• *Regular oversight of key clinical metrics including but not limited to: Days on Site (DOS), Monitoring Visit Report (MVR) and Follow up Letters (FUL) timelines, Action Items (AI) and other quality metrics, to ensure they are met and followed-up as necessary.
• *Oversight of visit report review and approval, including site issue escalation and resolution. This may involve direct review/approval of site visit reports, and interacting with the Central Visit Report Approvers, as appropriate.
• *Ensure clinical data is entered into the ICON CTMS or any other CTMS in a timely and accurate manner.
• *Contribute to the development and maintenance of all clinical elements of cross functional project plans.
• Able to work on multinational studies and may take the role of a Global CTM if appropriate.
• *Responsible for coordinating and managing the clinical project team to ensure:

o high performance and productivity (e.g. DOS for CRAs)

o optimal utilization

o minimal turnover

o all necessary project training is provided, documented and filed appropriately.
• *Responsible for documenting clinical risks and developing mitigation strategies and associated action plans, including issue escalation and resolution.
• Responsible for the development and maintenance of operational plans for clinical deliverables e.g. CRF completion guideline, Monitoring Plan, Recruitment Plan, Clinical Training Plan, annotated trip report etc.
• *Ensure the core clinical portions of the Trial Master File (electronic or paper TMF) are up-to-date and maintained in accordance with SOPs and the File Master Plan (FMP), including involvement in archiving as necessary. This includes documented QC checks of in house investigator site files.
• *Ensure all close-out activities are completed as necessary e.g. End of Trial (EOT) notifications sent, all payments made, CTMS updated, all visit reports finalized and all action items resolved.
• *Lead and/or actively participate in the conduct of clinical team meetings.
• *Ensure timely dissemination of information on study progress or issues and/or processes to all team members related to clinical deliverables and accurate tracking of any relevant study information related to clinical deliverables.
• *Implement QC activities, ensure compliance with quality measures and monitor required quality metrics.
• *Maintain confidentiality of information, as appropriate.
• Participate in business development activities such as bid defense meetings
• May be required to undertake individual, finite PM tasks under supervision and with support of the Line Manager.
• Participate in Company/Departmental initiatives, as requested.
• Undertake other reasonably related duties as assigned.

其他信息

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