Associate Director, Trial Supply Execution

Biopharma Asia; Horsham (PA); On-site; USD 140,000 - 242,000; Full time

Job summary

Johnson & Johnson is seeking an Associate Director, Trial Supply Delivery, to lead a team responsible for end-to-end clinical trial supply activities from study initiation through Last Patient Dosed. You will align strategy with portfolio priorities and ensure reliable delivery to depots and sites worldwide.

The role emphasizes risk management, budget oversight, inspection readiness, and cross-functional leadership across Global Clinical Operations, Quality, and Manufacturing.

Qualifications

• Bachelor's degree in supply chain, engineering, life sciences, or a related field is required; advanced degree preferred.
• Minimum of 8 years of relevant experience in clinical supply chain or related field.
• Demonstrated people leadership experience, including coaching and performance management.
• Strong knowledge of clinical trial operations, including distribution, RTSM/IRT, inventory management, quality systems, and GxP requirements.
• Demonstrated ability to build cross-functional alignment, influence stakeholders, and drive timely resolution.
• Ability to travel domestically and internationally up to 10%.

Responsibilities

• Lead a team of trial supply professionals and set clear priorities, accountabilities, and performance expectations across an assigned portfolio.
• Translate strategy into portfolio plans aligning with Clinical Supply Chain priorities and milestones.
• Ensure end-to-end trial supply setup and execution to deliver clinical supplies to depots and sites.
• Provide portfolio-level oversight of startup readiness, inventory health, site delivery, and inspection readiness.
• Serve as the primary escalation point for complex trial supply issues and coordinate with Global Clinical Operations, Quality, and external providers.
• Use metrics and dashboards to identify gaps, implement corrective actions, and drive continuous improvement.
• Manage budgets, external spend, and resource allocation with transparent risk reporting.

Skills

People leadership

Portfolio management

Risk management

Budget management

Cross-functional partnering

Decision-making

Education

Bachelor's degree in supply chain, engineering, life sciences, or related field

Tools

Power BI

SAP

ERP systems

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

Belgium R-109441, United States of America R-105213

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

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 Associate Director, Trial Supply Execution.

Candidates must already have authorization to work in the country of employment. Immigration sponsorship and relocation support are not available for this position. Candidates authorized to work pursuant to a short-term status (e.g., F-1) who require future immigration sponsorship are not eligible.

Purpose: The Associate Director, Trial Supply Delivery is accountable for leading a team of trial supply professionals responsible for the end-to-end setup and execution of clinical trial supply activities from study initiation through Last Patient Dosed. Reporting to the Head Trial Supply Delivery, this position translates the Trial Supply Delivery strategy into portfolio priorities and consistent operational execution. The role ensures reliable delivery of clinical supplies to depots and investigative sites worldwide, supports uninterrupted patient dosing and clinical development milestones, and provides leadership for risk management, issue resolution, performance, budget management, inspection readiness, and team capability development.

You will be responsible for:

Lead a team of trial supply professionals and establish clear priorities, accountabilities, performance expectations, and ways of working across an assigned portfolio of clinical trials.

Translate Trial Supply Delivery strategy and functional objectives into portfolio plans that align with Clinical Supply Chain priorities, Global Clinical Operations needs, and clinical development milestones.

Ensure end-to-end trial supply setup and execution to deliver clinical supplies to depots and investigative sites when and where needed to support uninterrupted patient dosing.

Provide portfolio-level oversight of startup readiness, inventory health, site delivery, patient supply continuity, issue resolution, and inspection readiness using defined metrics and performance reviews.

Serve as the primary escalation point for complex trial supply execution issues and partner with Global Clinical Operations, Quality, E2E Planning, Manufacturing, Logistics, Procurement, and external service providers to drive resolution.

Lead proactive risk identification, prioritization, mitigation, recovery planning, and closure for issues that could affect patients, study milestones, timelines, quality, compliance, or budget.

Use dashboards, analytics, and trend data to identify performance gaps, establish corrective actions, improve resource decisions, and drive continuous improvement.

Manage assigned operating budgets, external spend, workforce capacity, and resource allocation while maintaining transparent visibility of risks and variances.

Build strong cross-functional partnerships and communicate portfolio performance, constraints, decisions, and mitigation plans clearly and in a timely manner.

Recruit, onboard, coach, develop, and manage the performance of team members while strengthening engagement, empowerment, accountability, and succession readiness.

Implement and continuously improve standard processes, governance routines, escalation pathways, and operational playbooks to increase consistency, efficiency, quality, and compliance.

Ensure activities comply with GxP requirements, quality standards, company policies, and applicable regulations; support audits, inspections, investigations, and corrective and preventive actions.

Contribute to cross-functional initiatives that simplify processes, strengthen supplier and operational performance, increase digital enablement, and improve the stakeholder experience.

Qualifications/Requirements:

Minimum of a Bachelor's degree in supply chain, engineering, logistics, life sciences, pharmaceutical sciences, business, operations management, or a related discipline is required; an advanced degree is preferred.

Minimum of 8 years of relevant experience in clinical supply chain, pharmaceutical operations, clinical development, logistics, supply operations, or a related field.

Demonstrated people leadership experience, including direct management of professional employees, coaching, performance management, talent development, and resource allocation.

Strong knowledge of clinical trial operations and clinical supply execution, including distribution, RTSM/IRT, inventory management, logistics, quality systems, and GxP requirements.

Demonstrated experience managing complex portfolios, operational risks, escalations, budgets, suppliers, and competing priorities in a global, matrixed organization.

Proven ability to build cross-functional alignment, influence stakeholders, facilitate decisions, and drive issues to timely resolution.

Demonstrated ability to establish and use metrics, dashboards, governance processes, and standard ways of working to improve performance.

Strong strategic thinking, problem-solving, communication, stakeholder management, and decision-making capabilities.

Other requirements

Advanced proficiency with Microsoft Office applications; experience with Power BI or comparable data-visualization tools is preferred.

Experience with clinical supply and enterprise systems such as RTSM/IRT, SAP or comparable ERP platforms, inventory-management systems, financial systems, and reporting tools.

Knowledge of continuous improvement methodologies, including Lean, Operational Excellence, or similar approaches.

Ability to lead global and virtual teams effectively in a complex, cross-cultural, matrixed environment.

Ability to work across regions and time zones in support of global clinical trial execution.

Ability to travel domestically and internationally up to 10%.

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is :

$140,000.00 - $241,500.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:

Vacation –120 hours per calendar year

Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year

Holiday pay, including Floating Holidays –13 days per calendar year

Work, Personal and Family Time - up to 40 hours per calendar year

Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child

Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year

Caregiver Leave – 80 hours in a 52-week rolling period10 days

Volunteer Leave – 32 hours per calendar year

Military Spouse Time-Off – 80 hours per calendar year

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.

For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits

Johnson & Johnson is an 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, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.

If you are under 18 years of age you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent’s consent for the background check.