Culture & Values
Subsidiaries & Joint Ventures
Diversity & Inclusion
Sustainability & ESG Report
Safety & Toxicology
Data Management and Statistical Analysis
Clinical Development Strategy
Site Management (SMO)
Medical Device / IVD
Multi-region Clinical Trial (MRCT)
Vaccine Clinical Trial
Functional Service Provider (FSP)
Associate Global Project Director
To lead both Tigermed and sponsor teams to implement projects across regions as per sponsor requirements and in compliance with Tigermed policies/SOPs, ICH-GCP and local regulations. To ensure project meets all deliverables with adherence to the contractual agreements in terms of time, quality/scope, and cost;
Associate GPD provides cross-functional leadership to both sponsor and Tigermed teams to achieve operational excellence and project deliverables. To ensure generation of revenue of responsible projects and customer satisfaction. Associate GPD acts as a role model and/or mentor for the responsible Tigermed project teams. Associate GPD may represent Tigermed to speak at external professional conferences. Associate GPD is required to actively participate in other Tigermed initiatives such as process improvement including professional input/review on Tigermed SOPs and systems to contribute to Tigermed globalization process
Lead the implementation of responsible projects to achieve project finance goals from Bid Defense preparation, proposal, to project budget, revenue and profit etc.
Acts as the escalation liaison for the sponsors and instructor for GPMs/PMs of the responsible studies.
Supervise global communication according to PMP to proactively manage risks for the responsible studies.
Ensure the responsible study teams meet the sponsor contractual, organizational and relationship needs/expectations.
Ensure the GPMs/PMs provide regular reporting on project metrics, status of deliverables and risks/issues with the associated management plans to the sponsors.
Supervises and instructs the GPMs/PMs to chair and lead sponsor meetings.
Bachelor degree or above in Medical, Pharmacology or Biology related major. College diploma can be accepted if the personal attributes and relevant project management experience are sufficiently justified;
Adequate knowledge of current drug development processes and regulations, including local regulations, GCP, clinical trial operations. Current GCP certificate required Business skills such as budgeting and b usiness knowledge are a bonus;
A minimum of 13 years industry experience, including a minimum of 8 years project management experience, CRO work experience preferred;
Fluent in both written and spoken English, local languages fluency is preferred;
Excellent command of Microsoft offices;
Other abilities such as communication skill/Information analysis skill.