Offer summary

Qualifications:

Bachelor's or Master's degree in biology, pharmacy, health-related discipline, international trade, business administration, or logistics., Extensive experience in the pharmaceutical, clinical research, or consulting industry is mandatory., Strong competencies in financial tasks such as budgeting and cost negotiations are required., Fluency in English, both oral and written, is mandatory. .

Key responsibilities:

Provide global leadership and oversight for Clinical Trial Supply & Logistics projects.

Develop and execute the Clinical Trial Supply and Logistics strategy and ensure financial performance.

Lead CTS&L teams and develop solutions to achieve operational excellence and project delivery.

Act as Project Leader for standalone projects or those with limited services, ensuring compliance with regulations.

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 and logistic project Manager (SLPM) acts as the functional leader and will provide global leadership, management, general oversight, and direction for Clinical Trial Supply & Logistics (CTS&L) projects.

This requires in-depth business understanding in order to make effective decisions independently and the knowledge and experience to confidently recommend a course of action.
The SLL leads the CTS&L teams by combining a depth of clinical & Lab logistics experience with insight into client pressures and an ability to develop the right solution for the client to achieve operational excellence, delivery of projects/programs on time, to budget, to the highest quality and in compliance with ICH GCP, GCLP, customs regulations and GMP.

The SLL has overall accountability for the development and execution of the Clinical Trial Supply and Logistics strategy and financial performance of the project.

May act as Project Leader for CTS&L standalone projects or for projects involving a small number of services, where no other PAREXEL Project Leader is assigned.

What we expect from you:

Excellent understanding of logistics operations
Extensive experience in the pharmaceutical/Clinical research/consulting industry - MANDATORY.
Strong competencies in leading financial tasks such as budgeting, revenue recognition, change in scope analysis, cost negotiations, and financial metrics analysis - MANDATORY
Profound experience in laboratory logistics and/or clinical supply chain management or related field within the biopharmaceutical industry (MANDATORY)
Project management and/or significant team leadership experience
Individuals should have a strong understanding of cross-functional activities
Profound multinational work experience
Fluent in English (oral and written) - MANDATORY

Skills:

Client focused approach to work
A flexible attitude with respect to work assignments and new learning
Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
Operational Leadership and Project management skills
Proven strong business and commercial acumen
Proven consultative selling and negotiation, communication and customer management skills
Proven leadership and interpersonal skills
Ability to Mentor, give work instructions, encourage, train and support team members
Ability to develop creative solutions for any Clinical Supply Chain aspect, incl. PLD services
Sound operational understanding of Clinical Studies and related Supply Chain aspects
Global team management and development skills
Self- Motivated with a professional attitude
Capacity to work effectively in a matrix environment and value the importance of teamwork
Proficient use of MS office suite
Willingness and ability to travel as required
Excellent interpersonal, verbal and written communication skills
Good understanding of the GxP regulatory framework

Education:
Educated to B.A/ B.S. or Master's 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

Required profile