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CPM

Philippines, Australia, EU, US,Hong Kong China

Job Location

Philippines, Australia, EU, US, Hong Kong China

Job Purpose

To draft and implement project management effectively, and clinical operation conducting for related projects to insure that clinical research affaires works 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 qualify ensurance;
Manages project scopes and project costs timely to ensure control of project financial risk;
Ensures adherence to company SOP, policies and guidelines at the project level;
Ensures project s comply with Tigermed processes and systems such as CTMS, OA eTMF etc., including escalation to relevant functional and operational management;
Proactively attends bid defense process;
Perform necessary training for Project team colleague and build the effective team;
Provides feedback on proj ect team member’s performance to respective line managers.

Qualifications

Bachelor degree or above in Medical, Pharmacology or Biology related major; Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures; A minimum of 10 years’ industry experience, including a minimum of 6 yea rs’ project management experience, CRO work experience preferred. If outstanding PM achievement is shown, suitable candidate will be considered; Fluent in both written and spoken English；Local languages fluency is preferred; Good skills on Microsoft Word, Excel, PPT and Outlook, etc.; Other abilities such as Communication skills/Information-gathering skills. Knowledge and/or experience in medical practice is a plus.