Clinical Supplies Project Manager

Posted 11 Hours Ago
Be an Early Applicant
Blue Bell, PA, USA
In-Office
Mid level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
As a Clinical Supplies Project Manager, you will oversee drug supply planning, manage logistics for clinical trials, coordinate distribution, and ensure compliance with regulations while maintaining stakeholder communication.
Summary Generated by Built In
Clinical Supplies Project Manager - Remote, US

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are looking for a Clinical Supplies Project Manager to provide scientific and technical support to projects that have significant Pharmaceutical Supply Management, and Clinical Supplies activities associated with them and to act as the lead on appropriate project teams. You will be managing global pharmaceutical supply for all phases and pharmaceutical development activities on-going at contract facilities with respect to technical, quality, timing and cost standpoint on behalf of our clients.

What you will be doing:

  • Help to develop drug supply planning strategy and overall management of supplies for clinical studies.
  • Generates initial and revises drug forecast at study and program level, communicating demand requirements to CMC and other stakeholders.
  • Coordinates the procurement activities for comparator and  NIMP and/or ancillary supplies.
  • Interprets relevant protocol information to develop packaging/labeling design for clinical supplies.
  • Establishes distribution strategy and manages packaging/distribution timelines.
  • Supports design and set-up of IRT system.
  • Coordinates the origination, proofing and transition of clinical study labels.
  • Proactively communicates drug supply delivery timelines to appropriate stakeholders.
  • Coordinates the required documentation and activities for import and export of clinical supplies.
  • Monitors global inventory and proactively communicates with all stakeholders to ensure adequate quantity and timely delivery of clinical supplies throughout duration of a trial.
  • Monitors and manages retest dating for assigned study supplies.
  • Proactively identifies potential risks, provides corrective plans, and resolves clinical supply issues and complaints.
  • Provides information to support financial planning for global studies and monitors drug supply study budget.
  • Reviews new proposal requests and determines required clinical supplies management support.
  • Provides responses to potential new client request for information related to clinical supplies management

Job Requirements:

  • Bachelor degree required (Advanced degree nice to have)
  • Drug Forecasting (Off the protocol preferred) or Demand Planning experience required.
  • 3 plus years of prior experience in a pharmaceutical, biotech and clinical supply logistics environment preferred
  • Cell and Gene Therapy expertise preferred
  • Working knowledge of the Clinical Trial Supply process
  • Strong experience and skills in the management of clinical supply chain logistics.
  • Knowledge of regulations governing investigational products, including GMP and ICH/GCP guidelines
  • Knowledge of project management and Clinical customer relationship building

Benefits of Working in ICON:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

#LI-MH1

#LI-REMOTE

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements

  • A range of health insurance offerings to suit you and your family’s needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.

  • Life assurance

  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values.   We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

Top Skills

Clinical Trial Supply Process
Demand Planning
Drug Forecasting
Gmp
Ich/Gcp Guidelines
Irt System
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The Company
HQ: Dublin
34,685 Employees
Year Founded: 1990

What We Do

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

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