Job Description
Detailed Job Description:
- Provide business, technical and administrative support to the Global Clinical Supply business functions for a top pharma.
- Strong understanding of Interactive Voice Response (IVR) and Interactive Web Response (IWR) systems in clinical trials.
- Strong understanding of the end-to-end clinical trials process.
- Strong knowledge of protocol development, trial design, randomization, and clinical trial supply chain business.
Responsibilities:
- Responsible for working with study teams and supply chain regarding study design, packaging design, and dosing design decisions as they relate to the IRT vendor.
- Primary point of contact during study start-up, development, user acceptance testing, and production support; responsible for facilitating the implementation.
Desired years of experience:
Education/Certifications (Required):
Additional Information
All your information will be kept confidential according to EEO guidelines.
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