Your job will include performing a number of duties outlined below, but not limited to, with minimal or no supervision:
- Ensuring functional and compliant Project Management department by efficient planning and managing complex R&D projects from inception to launch, execution of 505(b)2, Generic first to file; first to market; clinically and logistically challenging projects.
- Ensuring collaboration among R&D, Clinical Development, Production and Cross Functional Teams (CFTs) to enable timely project delivery.
- Define and implement a robust project review mechanism to address escalations and mitigate risks.
- Manage co-development projects with multi-national partners
- Provide digital dashboards to senior management to track the status of deliverables (filings and milestones)
- Collaborate with business to showcase R&D capabilities to potential partners for co-development projects.
- Prepare and manage annual budgets.
- Representing the Project Department in meetings with FDA & corporate project reviews.
- Staying updated with recent practices and trends in the generic pharmaceutical industries and project management tools.
- Providing scientific and technical guidance to management on new project management models and suggests alternatives.
- Ability to effectively manage multiple projects, duties and assignments.
- Any other task assigned to you by the company officers and/or designated management staff from time-to-time.
Didn’t find the job appropriate? Report this Job