Clinical Supply Specialist

Job Purpose:
The Clinical Supply Specialist (CSS) will support the Clinical Supply Leader with the development and applying the study specific supply chain strategy including the sourcing and distribution strategy and the technical management for Clinical Trial Supply and Logistics projects.
The CSS supports the Clinical Trial Supply and Logistics teams by applying and executing supply chain to achieve client satisfaction and delivery of projects /programs on time, to budget, to the highest quality and in compliance with ICH GCP and GxP.
Key Accountabilities:

• Engaging with Clinical Supply Leader to develop logistics concepts and solutions in order to meet the client’s satisfaction and meeting the profitability of the projects.
• Keeping up to date with study scope and progress to ensure that study/project timelines and budgets are met in accordance to the contractual agreement including proactive management and communication of any changes and/or risks.
• Ensure that study specific management tools and documents are in place.
• Management of resources assigned to the project to ensure the CTSL FTE assigned is appropriate and meeting the study’s requirement.
• Pass Thru Cost (PTC) management with controls and reporting of costs for internal service fees and external providers.
• Collaborate with team to develop a clinical supply, sourcing and Management.
• Communicate with 3rd party providers and negotiate scope of work.
• Develop supply schedule, seek feedback from Clinical team on study progress and adjust accordingly and provide feedback to depots.

Skills:

• Client focused approach to work
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
• Proven consultative selling and negotiation, communication and customer management skills.
• Ability to support team members.
• Ability to develop creative solutions.
• Sound operational understanding.
• Self- Motivated with a professional attitude.
• Capacity to work effectively in a matrix environment and value the importance of teamwork.
• Basic Project management skills
• Proficient use of MS office suite
• Excellent interpersonal, verbal and written communication skills
• Good understanding of the GxP regulatory framework

Qualifications

Knowledge and Experience:

• Extensive experience of pharmaceutical/Clinical research/consulting industry.
• Profound experience in clinical logistics or related field within the biopharmaceutical industry.
• Individuals should have a strong understanding of cross functional activities
• Profound multinational work experience.
• Fluent in English

Education:

• Educated to B.A/ B.S. or Master degree, or equivalent (e.g. Pharm. D.), in biology, pharmacy, or other health –related discipline, international trade, business administration or logistics or relevant work experience

EEO Disclaimer

Parexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.