What are the responsibilities and job description for the Clinical Specialist position at US Tech Solutions?
Title: Clinical Studies Specialist II
Major Responsibilities:
Planning, scheduling, coordination, and execution, in support of clinical supply project manager to ensure the timely availability of investigation drug supplies and related services to clinical sites and depots.
Translates stability and packaging requests into an executed packaging design.
Identifies, develops, communicates, and tracks task completion dates , activities, logistics, and milestones in support of clinical supply project manager to ensure the timely availability of investigation drug supplies.
Responsible for creating appropriate protocol specific manufacturing and packaging work orders in concert with the clinical supply project manager.
Responsible to complete tasks identified for the team.
Responsible for inventory management system set up activities (i.e., Material masters, manufacturing requests, etc.) to support clinical packaging operations.
Critical Success Factors:
A basic understanding of clinical development and global supply chain requirements.
Competent in the application of standard business requirements (for example SOPs, Global Regulations).
Understanding the importance of compliance in a regulated environment and be capable of applying this knowledge to daily work.
Ability to work effectively and professionally with those in the dept as well as QA, Analytical and any area interface.
Education Requirement:
Bachelor’s Degree required preferably in physical science, math, engineering, pharmacy or data science.
Experience 2 - 4 years total experience in the Pharmaceutical Industry.
Salary : $25 - $30
