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R&D Operations

Senior Trial Supply Lead

  • Titel Senior Trial Supply Lead
  • Fungsi R&D Operations
  • Sub Fungsi Clinical Supply Operations
  • Golongan Experienced Analyst, Clinical Supply Operations (P5)
  • Location Titusville, New Jersey, United States; Horsham, Pennsylvania, United States; Beerse, Antwerp, United States
  • Posted
  • ID Permintaan 2406187681W
Melamar Sekarang
Bagi

Deskripsi

Johnson & Johnson Innovative Medicine Supply Chain, is recruiting for a Senior Trial Supply Lead located in Horsham, PA, Titusville, NJ or Beerse, Belgium.

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/

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

Clinical Supply Chain (CSC) holds the responsibility of global clinical supplies of the Janssen 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.

Key Responsibilities:

  • Adapt supply strategies in view of changes in trial execution and ensure seamless transition from study design phase
  • Assess clinical study recruitment rates vs forecast, study assumptions vs. actuals, and determine where action needs to be taken, e.g. flag supply risk or budget impact
  • Utilize business tools (e.g. IRT) to manage inventories at depots and sites, ensuring on-time delivery of clinical supplies for patient dosing.
  • Establish and modify trial specific distribution agreements
  • Member of appropriate GCDO clinical trial teams
  • Develop strong internal collaboration with the GCDO stakeholders to ensure customer satisfaction at both the trial and compound level
  • Develop excellent working relationships with the other groups within Supply Management
  • Manage trial supply budget.

Kualifikasi

Education:

  • A University/Bachelor’s degree (or equivalent experience) is required

Experience and Skills:

Required:

  • A minimum 6 years of experience preferably in a clinical supply related role is required
  • General knowledge of GxP principles is required
  • Excellent written and verbal communication skills, able to communicate clearly, making the complex clear and compelling to all levels of the organization in both written and oral forms isrequired
  • Strong project execution and cross-functional coordination skills, able to build strong collaborative teams and relationships, leading cross functional/ virtual teams where required, contributes to employee engagement is required
  • Gathers diverse viewpoints and able to influence key stakeholders within the Clinical Supply Chain, and other key cross functional partners is required
  • Foundational understanding of clinical trials and underlying dynamics to optimize global P&L and Distribution processes and interdependencies with Clinical Operations is required
  • Strong attention to detail, ability to work independently with limited coaching, and ability to multi-task and manage complexity is required
  • Ability to work in a high-pressure environment, acts with speed, flexibility, and accountability to achieve goals, solutions oriented, Integrity and Credo Based Actions is required

Preferred:

  • Experience with the following functions: clinical supply pack/label/distribution, clinical trial operations, project management, pharma/bio research and development, inventory management is preferred
  • Experience with clinical supply demand management tools preferred (e.g., IVRS, SAP, OMP+) is preferred
  • Intermediate to advanced software skills (e.g., Microsoft Excel, OneNote, PowerPoint) is preferred
  • Responsible for the management of all clinical supplies during trial execution (large and small molecules and for all phases of J&J clinical trials) is preferred

The anticipated base pay range for this position is $88,000 - $141,450 USD

The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/ performance year. Bonuses are awarded at the Company’s discretion on an individual basis.

Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

Employees are eligible for the following time off benefits:

  • Vacation – up to 120 hours per calendar year
  • Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar year
  • Holiday pay, including Floating Holidays – up to 13 days per calendar year
  • Work, Personal and Family Time - up to 40 hours per calendar year

Additional information can be found through the link below.

For additional general information on Company benefits, please go to:

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com

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