Clinical Supplies Manager II

Exelixis•Alameda, CA

5d•$132,500 - $188,000•Onsite

About The Position

The Clinical Supplies Manager II oversees all aspects of clinical supply management including packaging, labeling, monitor inventory levels, and distribution by interacting with internal and external supply partners/vendors to ensure supply of IMP are sufficient at depots and clinical sites.

Requirements

BS/BA degree in related discipline and a minimum of seven years of related experience; or, MS/MA degree in related discipline and a minimum of five years of related experience; or, Equivalent combination of education and experience.
Demonstrated experience with clinical supply management planning, labeling, packaging, and distribution.
Clinical Supply management experience using contract manufacturing companies strongly preferred.
Working knowledge and experience with Interactive Response Technologies (IRT) such as IVRS and IWRS
Knowledge of GMP batch record development, review, and approval processes.
Knowledge of Interactive Voice/Web response systems for use in clinical studies.
Working knowledge of regulations relating to clinical labeling, packaging and distribution activities.
Working knowledge of GMP/GCP/GLP regulations required.
Excellent project management and communication skills.

Nice To Haves

Certification in assigned areas is a plus.

Responsibilities

Lead effort for clinical supply management functionality.
Monitor and manage clinical supply activities through IRT from study start-up through study closure.
Proactively drive the labeling, packaging, release, distribution of clinical supplies at external CMO’s for assigned studies, ensuring the project timeline is met or exceeded.
Ensure domestic and global distribution arrangements are in place with external vendors to allow shipment following availability of technical and regulatory releases.
In collaboration with relevant partners, create forecasts and packaging design based on study needs to ensure optimized supply plan.
Partner with key stakeholders (including Quality Assurance and Regulatory Affairs) to ensure supplies are labelled and released for clinical site shipment for global clinical trials.
Work cross-functionally to develop IRT to develop specifications and perform UAT.
Design and/or review label text to meet product requirements and ensure compliance with US and international regulations.
Represent clinical supplies function at clinical trial team meetings; communicate plan and timelines to internal and external customers and partners.
Work with cross-functional teams to develop specifications and user testing of IRT systems provided by 3rd party vendors.
Ensure appropriate system documentation is transferred to TMF and ready for inspection readiness.
Utilize appropriate software and IT systems to effectively manage key project activities.