Remote Global Clinical Supplies Project Manager

Jobtome

Myrtle Point (OR)

Remote

USD 90,000 - 140,000

Full time

6 days ago
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Job summary

Thermo Fisher Scientific in the United States is seeking a Project Manager Clinical Supplies to oversee end-to-end supply chain for clinical trials, ensuring timely distribution of trial materials and maintaining inventory levels. The role requires CRO industry experience and a Bachelor's degree or equivalent, with remote work options for US locations.

You will coordinate with cross-functional teams, develop study plans, manage risk, and mentor junior staff while adhering to GxP requirements and

Qualifications

  • CRO industry experience is a requirement.
  • Bachelor’s degree or equivalent required.
  • 5+ years of relevant experience in clinical supply management.

Responsibilities

  • Develop study specific plans for each assigned project.
  • Meet with internal teams to coordinate efforts and update project reports.
  • Integrate clinical supplies activities into the supply chain to support logistics and GxP compliance.
  • Participate in ongoing training on new regulations.
  • Represent the department at meetings and initiatives as required.
  • Mentor and guide junior team members.
  • Participate in process improvement initiatives.
  • Maintain and use existing tools and seek improvements.
  • May participate in client contact for supply chain inquiries.

Skills

Project management
Leadership
Communication skills
English proficiency
MS Office proficiency
Attention to detail
Teamwork
Problem solving
Multi-tasking
Customer service

Education

Bachelor’s degree or equivalent

Tools

Microsoft Office

Job description

Thermo Fisher Scientific in the United States is seeking a Project Manager Clinical Supplies to oversee end-to-end supply chain for clinical trials, ensuring timely distribution of trial materials and maintaining inventory levels. The role requires CRO industry experience and a Bachelor's degree or equivalent, with remote work options for US locations.

You will coordinate with cross-functional teams, develop study plans, manage risk, and mentor junior staff while adhering to GxP requirements and

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