Clinical Supply Chain Specialist

BeiGene

9d•$79,100 - $109,100

About The Position

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: Under the supervision of the direct manager or team lead, the Specialist of Clinical Supply Chain manages drug supply activities related to planning, label development, label & pack, and distribution for clinical trials. With the guidance of the manager or team lead, actively develops and oversees supply plans to ensure accurate and continuous supply to patients while reducing risk and minimizing waste. With guidance, may participates on teams to develop and implement process improvements to build the organization for the future.

Requirements

2+ years progressive experience in Supply Chain preferably within the biotech, pharmaceutical, CRO, industry.
Proficient in Microsoft Word, Excel, and Outlook
Good analytical, communication and interpersonal skills.
Good organizational and effective time management skills.
Good problem-solving and risk management skills.
Good at Microsoft Office Tools

Nice To Haves

Bachelor’s degree or above in Medicine/science related, or supply chain/management/operation related, or equivalent combination of education, training and experience.

Responsibilities

Work with team lead or manager to understand clinical demand requirements and ensure alignment with study teams to supply plans and timelines.
Collaborate and liaise with internal (e.g. Clinical Operations, Regulatory, Quality, CMC) and external stakeholders (e.g. CMOs, IRT vendors) appropriately.
With guidance, outline supply strategies to maximize supply efficiency, minimize waste while identifying risk and develop risk mitigation plans.
Work with team lead or manager to create supply and inventory plans and develop production schedules for clinical trial materials.
Monitor schedule adherence of production schedules and make course corrections if needed.
Work with label management team to ensure label text and proofs are in accordance with applicable rules, regulations, product specifications, and clinical study protocol(s).
Assist with comparator sourcing team to conduct developed comparator sourcing strategies/activities.
Support IRT user acceptance testing, develop IRT supply strategy (DNX parameters), and oversee ongoing supply activities in system.
Coordinate and track bulk shipments to CMOs, depots, and vendors. Maintain and track import licenses.
Participate in performing UAT acceptance testing for IRT systems
Supports IRT related activities to ensure adequate supply for clinical trials
Additional responsibilities as required