Join our Talent Network
Skip to main content

< Back to Search Results

Senior Clinical Supplies Management Specialist

Location: Madison, NJ, United States
Job Type: Contract
Job Category: Pharmaceutical and Biotech
Job Industry: Biotechnology/Medical Devices
Salary: The pay we're offering is $52 per hour
Save Job Saved

Apply now and our proprietary system will quickly have you in front of a live recruiter.

The Opportunity


We're looking for a Senior Clinical Supplies Management Specialist, working in Biotechnology/Medical Devices industry in Madison, New Jersey, United States.

Job description:
  • Develops and implements the initial timeline, budget, drug supply forecasts and component requirements needed for preparation of the Clinical Supply Master Plan for Phase I through IV clinical protocols.
  • Effectively organizes and conducts meetings, and demonstrates facilitation and listening skills.
  • Consistently demonstrates skills for evaluating customer needs and offering alternatives to accomplish project goals.
  • Reviews Clinical Research Development programs and coordinates development of yearly clinical supplies forecasts and supply plans.
  • Protocol interpretation and breakdown.
  • Demonstrates planning, project management, negotiation and presentation skills.

Our Client

Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.

Experience Required for Your Success

  • Bachelors Degree
  • 6+ years of Clinical Supply/Clinical Packaging/Project Coordination experience in the pharmaceutical/device industry or CRO
  • Knowledge cGMPs and relevant FDA Regulations essential
  • Excellent communication and writing skills
  • Proficiency in Microsoft Office and Microsoft Project
  • High level of professionalism
  • Ability to prioritize, planning and problem-solving
  • Ability to handle multiple projects and work in a team environment
  • Ability to operate, with composure and confidence, in a team or matrix environment
  • Effective influencing skills

What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply Now

Share: mail

Similar Jobs