Clinical Supply Chain Specialist

GlobalChannelManagementInc

Cambridge, MA, United States contract

Posted: June 24, 2017

Quick Summary

A Clinical Supply Chain Specialist is responsible for managing the supply chain for pharmaceutical products, ensuring timely and efficient delivery of products to customers. The ideal candidate will have experience in life sciences and project management, with a strong understanding of clinical development and supply chain operations.

Job Description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.

• Minimum 1-3 years in life sciences industry related
experience, including Project Management, Pharmaceutical Development,
Clinical Supply Management, and/or Clinical Trials Coordination.

• At least 1 year direct experience in clinical supplies environment.

• Proficient knowledge of Microsoft Excel, PowerPoint, and Project software required.

• APICS certification (CPIM, CLTD, CSCP) preferred.

Bachelors in life sciences or business major or equivalent required.

Skills:Required

• SUPPLY CHAIN
• UAT TESTING
• CLINICAL STUDY PLANNING
• CLINICAL TRIAL
• CLINICAL MONITORING

• Review clinical trial protocols and understand impact to identify
demand assumptions based on enrollment rate, number of sites, number of
countries, etc.

• Assist with the creation, review, and updating of clinical supply and demand plans.

• Communicate
and update clinical supply requirements on study and program levels to
supply chain project leads and ensure seamless coordination of demand
and supply.

• Ensure changes in supply configuration, trial
design, enrollment timeline, manufacturing availability and regulatory
requirements are considered.

• Monitor inventory levels at
depots and clinical sites through the life of a trial; take preventative
actions to avoid potential supply issues.

• Coordinate shipping oversight of clinical product for worldwide studies.

• Manage drug returns process and site close-out activities.

• Prepare drug reconciliation reports.

• Assist with label development and management for clinical product.

• Assist in development of IWRS/IVRS and participate in User Acceptance Testing.

• Develop
packaging and supply strategies to maximize supply efficiency, minimize
waste while identifying risk, and develop risk mitigation plans.

• Communicate with external service providers on project requirements.

• Request and review quotes from providers.

$44/hr

6 months

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