Clinical Project Manager

To draft and implement project management effectively, and clinical operation conducting for related projects to ensure that clinical research affairs work smoothly.

Responsibilities:

• Acts as the primary liaison for the sponsors of the responsible studies.
• Leads and directs cross-functional team leaders and third parties/vendors.
• Manages project contractual deliverables in terms of project milestone payments and quality assurance.
• Manages project scopes and project costs timely to ensure control of project financial risk.
• Ensures adherence to company SOPs, policies, and guidelines at the project level.
• Ensures projects comply with Tigermed processes and systems such as CTMS, OA eTMF, etc., including escalation to relevant functional and operational management.
• Proactively attends bid defense processes.
• Performs necessary training for project team colleagues and builds an effective team.
• Provides feedback on project team members’ performance to respective line managers.

Qualifications:

• Bachelor's degree or above in Medical, Pharmacology, or Biology-related major. A 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, and clinical trial operations. Current GCP certificate required. Business skills such as budgeting and business knowledge are a bonus.
• A minimum of 10 years of industry experience, including a minimum of 6 years of project management experience; CRO work experience preferred. If outstanding PM achievement is shown, a suitable candidate will be considered.
• Fluent in both written and spoken English; local language fluency is preferred.
• Excellent command of Microsoft Office.