Project Manager - (Biotech/Biomedical)

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
  
  

Temp to perm: Possible depending on openings and performance

Position Summary:

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
  
  

Education:

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
  
  

Specialized or Technical Knowledge Licenses, Certifications needed:

• Project Management Professional (PMP®) preferred
• Excellent computer software skills, specifically – Planisware / Microsoft Project, SharePoint, PowerPoint, Word, Excel and Outlook
  
  

Functional Knowledge:

• In-depth knowledge of the Pharmaceutical drug development process
  
  

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.