Clinical project manager

Responsibilities:

l Take charge of the management and operation of clinical trial projects, coordinate cross-functional team(s) in the execution of clinical trials
l Set and manage goals and timelines for projects encompassed by the product strategy; building and maintaining project timelines and interdependencies
l Proactively communicate status of clinical trial deliverables to clinical management, core team, and other stakeholders including executive management
l Facilitate appropriate interim and final reviews of study data in preparation of regulatory submissions
l Manage clinical affairs through plans (mitigate clinical trial risk)
l Execute, negotiate and maintain supply agreements with suppliers
l Manage and facilitate resolution of clinical trial risks or issues; plan and implement
contingencies as appropriate.
l Meet with cross-functional Clinical Affairs team members to prepare team meetings, capture meeting minutes and assign key action items with single points of accountability

Qualifications:

l Abundant professional experiences of clinical trial as well as good understanding of related laws and regulations
l Demonstrated excellence in leadership. teamwork and communication skills including relationship building skills with team members, peers, and senior leaders
l Broad and thorough understanding of clinical trial process including: study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation and project finance accounting
l Able to manage numerous projects/conflicting priorities, and to be flexible when priorities change.
l Hard-working, clear thinking logic, result-oriented, willing to travel