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Vendor Strategy Director/Project Director - FSP - Remote

Role overview

Qualifications

  • Advanced degree in science or business, or equivalent relevant experience
  • 10+ years of relevant industry experience, including leadership within clinical operations
  • Strong understanding of clinical trial methodology, GCP, medical terminology, and clinical development processes
  • Excellent communication, planning, project management, analytical, and problem-solving capabilities

Responsibilities

  • Lead end-to-end supplier and vendor strategy activities across clinical development programs
  • Define and align program-level vendor strategies in partnership with key stakeholders
  • Manage and oversee supplier performance against established program objectives
  • Proactively identify, assess, and manage supplier risks and quality concerns

Key facts

Hard skills

Other skills

  • Quality Assurance
  • Strategic Thinking
  • Relationship Building
  • Influencing Skills
  • Communication
  • Planning
  • Analytical Skills
  • Problem Solving

About the company

Parexel logo

Parexel

Contract Research Organizations (CRO)

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.


About Parexel

Parexel is a leading global clinical development partner delivering insight-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose, moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry-leading innovation, With Heart® .


About the Role

We are seeking an experienced Vendor Strategy Director to serve as a strategic business partner for vendor activities across complex clinical development programs. In this high-impact role, you will collaborate closely with Clinical Operational Program Heads, Portfolio Innovation Directors, Procurement, and cross-functional stakeholders to define and execute end-to-end vendor strategies that support successful clinical trial delivery.

As the program-level leader for vendor strategy and performance, you will oversee supplier delivery across the clinical study lifecycle, from study startup through closeout, ensuring quality, compliance, operational effectiveness, and alignment with program objectives. This position offers the opportunity to influence global clinical development programs, drive innovation through strategic supplier partnerships, and contribute directly to the delivery of therapies that improve patient lives.


Key Responsibilities

  • Lead end-to-end supplier and vendor strategy activities across clinical development programs
  • Define and align program-level vendor strategies in partnership with Clinical Operational Program Heads, Portfolio Innovation Directors, Procurement, and alliance stakeholders
  • Manage and oversee supplier performance against established program objectives and strategic priorities
  • Proactively identify, assess, and manage supplier risks, quality concerns, and contract-related issues while driving continuous improvement initiatives
  • Anticipate future portfolio and program needs and translate upcoming demand into vendor service requirements
  • Partner with vendor alliance teams to identify, qualify, and engage suppliers that support evolving program needs
  • Enable early supplier engagement during protocol development and feasibility activities to support operational readiness
  • Serve as the primary point of contact and escalation for program-level vendor strategy and operational challenges
  • Drive productivity initiatives and oversee achievement of vendor-related performance objectives
  • Support inspection readiness and audit-related activities across programs
  • Provide operational and functional support to Trial Vendor Managers and Vendor Start-up Managers
  • Collaborate with global stakeholders to leverage innovative vendor solutions that enhance clinical trial execution and delivery

Candidate Profile

You'll thrive in this role if you bring:

  • Strengths in strategic thinking, business partnership, relationship building, and influencing across complex matrix organizations
  • Experience leading vendor strategy, outsourced clinical trial activities, and cross-functional clinical operations initiatives
  • The ability to build and maintain effective external partnerships and internal stakeholder relationships
  • A strong understanding of clinical development, clinical trial operations, and supplier management principles
  • Excellent communication, planning, project management, analytical, and problem-solving capabilities
  • The ability to navigate complex environments while balancing quality, timelines, innovation, and business priorities

Required Qualifications

  • Advanced degree in science or business, or equivalent relevant experience
  • 10+ years of relevant industry experience, including leadership within clinical operations and management of outsourced clinical trial activities at both operational and strategic levels
  • Strong understanding of clinical trial methodology, GCP, medical terminology, and clinical development processes
  • Experience with supplier services supporting clinical development programs and a strong understanding of trial management and trial monitoring activities
  • Knowledge of quality and regulatory standards relevant to clinical research and outsourced service delivery
  • Demonstrated success developing and managing strategic internal and external partnerships
  • Strong communication, organizational, leadership, and problem-solving skills
  • Fluent written and spoken English

Preferred Qualifications

  • Experience partnering with global, cross-functional clinical development organizations
  • Demonstrated executive leadership and strategic vendor management experience
  • Experience driving productivity initiatives and operational improvements across clinical programs
  • Experience supporting inspection readiness, audit preparation, and quality-focused supplier management
  • Track record of enabling successful international collaboration across diverse stakeholder groups

Benefits and Compensation

  • Health, Vision & Dental Insurance
  • Vacation/Holiday/Sick Time
  • Flexible benefit portal
  • Car or car allowance (only applicable roles)

If this job doesn't sound like the next step in your career, but perhaps you know of someone who'd be a perfect fit, send them the link to apply!


We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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