Offer summary

Qualifications:

Bachelor's Degree or equivalent experience, Minimum of 5 years of relevant experience in clinical trials or supply chain planning, Strong communication skills, both oral and written, Project management experience is highly desirable..

Key responsabilities:

Develop and manage supply strategies for clinical trials

Coordinate with clinical teams and oversee supply coordinators

Ensure timely delivery of materials and manage budgets

Lead or collaborate with stakeholders to resolve supply-related issues.

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.

Job Summary:

Seeking an Protocol Project Manager, Supply and Logistics to develop and manage supply strategies for clinical trials. The ideal candidate will lead study planning activities, coordinate with clinical teams, and oversee supply coordinators and logistics planners. Responsibilities include ensuring timely delivery of materials, collaborating with stakeholders, managing budgets, and resolving supply-related issues. The role requires strong supply chain management skills, clinical trial experience, excellent communication, and leadership abilities. May involve supporting special projects and mentoring team members.

Description of Roles and Responsibilities

Responsible for developing study specific supply planning strategies for ancillary supplies.

Serves as the primary interface to the clinical trial team and other functional partners for assigned studies.

Performs primary study planning activities for ASM.

Leads assigned Ancillary Supply Coordinator and Logistics Planner in ancillary supply study management activities.

Responsible for overall management of supply plan and supply activities for assigned clinical studies.

Develops ancillary supply strategy ensuring on time delivery of materials for assigned protocols.

Interacts with appropriate clinical and functional stakeholders to determine scope of study and ancillary supply requirements.

Ensures compliance with company SOP’s and business processes.

Provides study finance stakeholders with initial and updated ancillary supply budget reports

Utilizes appropriate tools & systems to plan initial ancillary supply needs and subsequent resupply activities

Leads or collaborates with stakeholders in evaluating and defining resolutions to issues regarding supplies and/or deliverables.

May support special projects or act as process SME

May deliver training or provide special support mentoring to new PPMs.

Skills Requirements:

Minimum of 5 years of relevant experience with clinical trials, clinical supplies, clinical research or supply chain planning

Effective communication skills both oral and written

Project management experience highly desirable

Highly detail oriented, flexible, and adaptable to changing needs

Motivated and driven to learn and develop skill sets

SAP experience a plus

Education Requirements:

Bachelor's Degree or equivalent 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.

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