AbbVie Project Manager in Tokyo-To, Japan
Research & Development
The Project Manager II is responsible to bring clinical programs to life through the execution of one or more Phase 1-4 clinical research programs. Contributes project management strategies to ensure clinical projects are executed with quality and efficiency, on-time, within budget, and meet company objectives. The project manager achieves these objectives via scientific expertise, strategic thinking, a global mindset and innovative solutions to address risks and challenges.
Responsible for problem solving, risk mitigation, and contingency planning at both program and project level.
Considered a Subject Matter Expert and competent in the application of standard business procedures (SOPs, ICH, Global Regulations, Ethics and Compliance)
Drive operational excellence within the organization for project success
Conduct training and coaching to staff based on the group manager’s direction
Effectively communicates project progress and actively identifies issues that potentially impact milestone achievement per plan and identify potential interventions or solutions to manage the issues
Create robust and challenging project plans and track the project plan and lead issue identification and problem solving in case of off track
Support for collaboration and effective interactions between LPT and stakeholders/governance
Support for cross-project/portfolio discussion
Partnering with LPH, create a project plan based in alignment with the global asset strategy, with consensus with the LPT
The PM has the principal accountability especially on the identification of the scope, WBS preparation, timeline, costing, and risk management plan.
Get an approval from ADT and necessary stakeholders for the project plan agreed in the LPT
Get the necessary budget for the execution of the project as based on the project plan
Monitor the project progress and have the accountability for the LBE
Have the accountability of major milestones and critical path of timeline of the project
Explain to senior management and governance on behalf of the LPH
Lead the discussion in the LPT to identify and solve problems if the project is not proceeding according to the project plan and put the project back on the right track. If the problems cannot be solved, propose an amendment on the project plan to the LPT.
Compile, organize and provide information necessary for the LPT in making decisions
Provide big picture context to the LPH/LPT to influence decision making
In partnership with the LPH, coordinate LPT meetings and facilitate the discussions therein
Drive the risk management to prevent the project from deviating from the plan
Lead cross-functional communication involving the functions other than the LPT members
Prepare the opportunities for discussion for maximization of collaboration with the stake holders, and hold meetings for such discussion
Bachelor's degree in Life Sciences or a relevant field. Advanced degree preferred (MSc / PhD / MBA) or strong demonstration of equivalent combination of relevant educational and professional training.
6+ years of experience on R&D related area, including 4+ years clinical development planning phase to approval.
Work experience in global environment.
Possesses good communication skills and leadership abilities, including verbal and written English skills (TOEIC over 750)
Must have demonstrated a high level of core and technical competencies through management of various phases of projects
Preferred exposure in project completion in multiple phases of projects (Phase 1-3, 4)
Industry knowledge in the Biotechnology, Pharmaceutical, or other Healthcare related field and understanding of its business
Required skills include:logical thinking and problem solving skills, leadership skills, team building and trust, building skills,conflict management skills, analytical and critical thinking skills