Clinical supply chain-Project Coordinator IV

Mindlance; New Haven (CT); On-site; USD 75,000 - 95,000; Full time

Job summary

A national recruiting company is seeking a Clinical Supply Chain-Project Coordinator IV located in New Haven, Connecticut. This role involves developing integrated supply plans for clinical trials, collaborating on demand forecasts, and coordinating with manufacturing teams. The ideal candidate has 5 years of experience in the pharmaceutical or biotech industry and strong analytical skills, particularly in Excel. Join a dynamic team committed to excellence in clinical operations.

Qualifications

• 5 years of experience in pharmaceutical or biotech.
• Experience in supply, planning, or logistics for clinical trials.
• Strong analytical skills with Excel expertise.

Responsibilities

• Develop integrated plans for clinical trial supplies.
• Work with clinical operations on demand forecasts.
• Create manufacturing timelines and production schedules.

Skills

5 years’ experience in the pharmaceutical or biotech industry

Experience working in supply, planning, or logistics supporting clinical trials

Strong analytical capabilities and experience working in Excel

Proven track record of working successfully on cross-functional teams

Education

BS in a relevant scientific discipline

Job description

Clinical supply chain-Project Coordinator IV

Contract

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at http://www.mindlance.com.

Summary

The clinical supply chain planner will be responsible for developing integrated plans to ensure sufficient supply for clinical trials. The planner will work with clinical operations to develop demand forecasts for each clinical program. Using these forecasts, he/she will then work with the external manufacturing team (DS, DP, and label/pack) and CMC leads to create manufacturing timelines and production schedules.

Skills

• 5 years’ experience in the pharmaceutical or biotech industry
• Experience working in supply, planning, or logistics supporting clinical trials
• Strong analytical capabilities and experience working in Excel
• Proven track record of working successfully on cross-functional teams

Education

BS in a relevant scientific discipline

All your information will be kept confidential according to EEO guidelines.