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Supply and Logistics Specialist

Role overview

Qualifications

  • Extensive experience of pharmaceutical/Clinical research/consulting industry
  • Educated to B.A/ B.S. or Master degree in biology, pharmacy, or other health-related discipline
  • Proficient use of MS office suite
  • Fluent in English

Responsibilities

  • Support the Supply Logistics Project Manager with developing study specific supply chain strategy
  • Manage resources assigned to the project to meet study’s requirements
  • Collaborate with team to develop clinical supply, sourcing, and distribution strategy
  • Identify and initiate process improvements

Key facts

Other skills

  • Negotiation
  • Microsoft Office
  • Teamwork
  • Communication
  • Detail Oriented
  • Self-Motivation

About the company

Parexel logo

Parexel

Contract Research Organizations (CRO)

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

The Supply & Logistics Specialist (SLS)/(Senior) Supply & Logistics Specialist (SrSLS) will support the Supply & Logistics Project Manager (SLPM) with the development and applying the study specific supply chain strategy incl. the sourcing and distribution strategy and the technical management for Clinical Trial Supply and Logistics projects.

The SLS/SrSLS supports the CTS&L 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.

The SLS/SrSLS has responsibility for the execution of the CTS&L strategy on the project.

Key Accountabilities:

Project Management 

  • Engage with SLPM to develop logistics concepts and solutions in order to meet the client’s satisfaction and the profitability of the projects
  • Keep 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
  • Manage resources assigned to the project to ensure the CTS&L FTE assigned is appropriate and meeting the study’s requirement

Financial Management

  • Pass Thru Cost (PTC) management with controls and reporting of costs for internal service fees and external providers.

Operational Strategy and Management

  • Collaborate with team to develop a clinical supply, sourcing and distribution strategy with relevant stakeholder and make sure that required documentation is in place
  • Communicate with 3rd party providers and negotiate scope of work in conjunction with procurement.
  • Develop and plan inventory according to strategy, quantities and forecast
  • Develop supply schedule, seek feedback from Clinical team on study progress and adjust accordingly and provide feedback to depots

(Senior) Ensure Quality and Process Improvement

  • Identify and initiate process improvements
  • Mentoring of Clinical Supply Specialists and Clinical Supply Assistants

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/Excellent 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/Very good understanding of the GxP regulatory framework

Knowledge and Experience

  • Extensive experience of pharmaceutical/Clinical research/consulting industry.
  • Profound/Superior experience in clinical logistics or related field within the biopharmaceutical industry.
  • Project management experience
  • 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

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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