Project Manager III
Role :- Project Manager III
Duration : 12+ Months
Location: West Chester, PA 19380
Onsite or Offsite: Working 3 days at the Office and 2 days Remote
Shift: Flexible
Core essential skill sets to be considered for the role:
Screenings
The Project Manager has shared responsibility for leading the global development of R&D products; ultimately to maximize the product’s potential. The PM will work in partnership with a Program Leader to establish, maintain and deliver the priority product plan for all development stages.
Required: Master’s level degree in life scientific field
Preferred: Advanced scientific degree (M.D., D.O., Ph.D.)
Experience
Duration : 12+ Months
Location: West Chester, PA 19380
Onsite or Offsite: Working 3 days at the Office and 2 days Remote
Shift: Flexible
Core essential skill sets to be considered for the role:
- Experience in project management in the pharma industry
- Good knowledge of the drug development process
Screenings
- Basic Background check
- 12 Panel Drug test
The Project Manager has shared responsibility for leading the global development of R&D products; ultimately to maximize the product’s potential. The PM will work in partnership with a Program Leader to establish, maintain and deliver the priority product plan for all development stages.
- Supports the cross-functional global program team to execute the strategic planning and delivery of the integrated development program
- Participate in selected expert team meetings (CDT, CMC, Preclinical, RA and any other meetings deemed essential)
- Lead monthly GPT meetings (including agenda, minutes and discussions)
- Responsible to co-chair with RA lead the Project Submission Team as required
- Proactively identify and manage risks and emerging issues and ensure related decisions are made at the appropriate levels and with the appropriate cross-functional input.
- Develop and manage end-to-end product plans in Planisware to accurately reflect the timelines and interdependent functional links and develop scenario plans when required
- Support team alignment for workplan (AOP/LRP) and governance processes and interactions and present to management when required
- Support creation of development documents (TPP, IDP, DPP, monthly reports, dash-boards etc.) and ensure all relevant program documentation are updated, approved by respective leadership and uploaded into the designated platforms
- Participate in GPL initiatives
Required: Master’s level degree in life scientific field
Preferred: Advanced scientific degree (M.D., D.O., Ph.D.)
Experience
- 5 years of experience in the pharmaceutical industry
- Experience in project management
- Experience working with external partners
- Preferred: Experience in Gx and Biosimilar drug development
- Established track record of effective and influential oral presentations
- Project Management Professional (PMP®) preferred
- Excellent computer software skills, specifically – Planisware / Microsoft Project, SharePoint, PowerPoint, Word, Excel and Outlook
- In-depth knowledge of the Pharmaceutical drug development process
-
Seniority level
Mid-Senior level -
Employment type
Contract -
Job function
Project Management and Information Technology -
Industries
Pharmaceutical Manufacturing
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