Clinical Supply Chain Specialist
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