Senior Clinical Supplies Project Manager

myGwork - LGBTQ+ Business Community; United States; On-site; USD 145,000 - 165,000; Full time

Job summary

A leading global company in the LGBTQ+ community is seeking a Senior Clinical Supplies Project Manager. The role involves developing drug supply strategies and managing clinical supplies for trials. Candidates should possess strong planning and management skills with a background in pharmaceutical or clinical settings.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Qualifications

• At least three years of experience in clinical supplies planning or supply chain management.
• Five years of experience in clinical supplies, clinical research or pharmaceutical development.

Responsibilities

• Manage clinical supply planning and forecasting for study protocols.
• Support financial planning for global clinical supplies.
• Monitor global clinical supply inventory at the clinical site level.

Skills

Supply Chain Management

Clinical Research

Drug Supply Planning

Education

Bachelor degree in scientific or pharmaceutical discipline

Job description

Senior Clinical Supplies Project Manager

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Senior Clinical Supplies Project Manager

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This job is with ICON plc, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

You will be responsible for developing drug supply planning strategy and overall management of supplies for clinical studies.

What You Will Be Doing

• Manage clinical supply planning and forecasting for study protocols
• Serve as member of clinical study team and/or clinical drug supply team, as assigned
• Interpret relevant protocol information to develop packaging/labeling design and/or global distribution strategy
• Support design and set-up of IRT system
• Support financial planning for global clinical supplies, including budgeting, forecasting, and strategic planning activities for clinical trials and pharmaceutical development pipeline
• Coordinate the origination, proofing and translation of clinical study labels, as required
• Monitor global clinical supply inventory at the clinical site level for both IRT and traditional studies via tracking of specific milestone dates and adjusting drug distribution plan accordingly
• Coordinate drug supply delivery timelines with Clinical, packaging source area(s), and indirectly with GMP laboratories, QA and Regulatory Affairs, as required
• Maintain close communications with all internal-chain groups to ensure the adequate supply of clinical supplies throughout the duration of a clinical trial
• Serve as ‘consultant’ for managers throughout the organization on issues related to clinical supplies and project management
  
  

You Are

• Bachelor degree or equivalent, preferably in a scientific or pharmaceutical discipline
• At least three (3) years of experience in clinical supplies planning/supply chain management, with (5) years of experience in clinical supplies, clinical research or pharmaceutical development
  
  

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 maximise 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 website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

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, colour, 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.

https://careers.iconplc.com/reasonable-accommodations

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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Project Management and Information Technology

• Industries

  Pharmaceutical Manufacturing

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