Associate Director, Trial Supply Lead

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
R&D Operations

Job Sub Function:
Clinical Supply Operations

Job Category:
People Leader

All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Titusville, New Jersey, United States of America

Job Description:

About Innovative Medicine:

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for an Associate Director, Trial Supply Lead to be located in Titusville, NJ or Horsham, PA,

Purpose:

Clinical Supply Chain (CSC) holds the responsibility of global clinical supplies of the Innovative Medicine Research & Development portfolio and the Global Medical Affairs portfolio.

Our activities include all in-house and outsourced manufacturing of clinical supplies (API, Drug Product, Packaged and Labeled Clinical Supplies), demand forecasting, supply planning, and global distribution of supplies.

Through a global network and organization we are responsible for the clinical supplies of Synthetics, Molecules and Bio Therapeutics and Advanced Therapies products in development and low volume commercial supply and secure the supply to more than 60.000 patients in more than 330 clinical trials every year.

You will be responsible for:



* Supervising a group of individuals responsible for:

Studying drug management for pharma R&D clinical trials.

Ensures 99.5% Successful Dose, optimized inventory levels, optimized campaigns and minimized waste for the trial.

Monthly demand planning with clinical teams and within CSC kit demand planning tools

Studying drug budgets (OOP$ and FTEs)


* Ensuring monthly cS&OP cycle adherence and takes leadership over the escalation and (where applicable) resolution of critical risks and issues.

Leads S&OP escalation topics with limited or no guidance.


* Supporting team to properly manage any study risks via the cS&OP process, while maintaining the highest standards of quality and compliance


* Driving team problem solving and acts as a coach to team members to drive their technical and personal development.


* Managing the activities required to m...