Senior Global Study Manager, Central Lab Services

BVB Labcorp BV

Belgique

À distance

EUR 90 000 - 120 000

Plein temps

14 jours+
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Résumé du poste

Labcorp is seeking a remote Senior Global Study Manager, Central Lab Services to join our Belgium team. You will lead global clinical studies, manage client communications, timelines, budgets, and risk, and partner with CROs and internal study teams.

Ideal candidates have extensive CRO/pharma experience, central labs background, and a track record of delivering complex studies on time and within budget.

Qualifications

  • Bachelor degree or higher in a relevant field.
  • 5+ years in pharma/CRO with global study management experience.
  • 5+ years client-facing and stakeholder management.
  • 2+ years Central Labs experience.
  • Master degree or PM certification preferred.

Responsabilités

  • Key contact for clients; liaison between Clients, CRO, and Labcorp CLS.
  • Provide project management oversight focusing on budget, risk, and milestones.
  • Manage a portfolio of global, high-complexity studies.
  • Ensure regulatory compliance and quality in study delivery.
  • Lead cross-functional teams to deliver on time and within budget.
  • Participate in CLFs and support continuous process improvement.
  • Foster strong internal and external relationships to meet client expectations.

Connaissances

Client facing & stakeholder management
Budget management
Project management
Global clinical trials
Leadership & communication
Risk management

Formation

Bachelor degree
Master degree or University degree
PMP or Prince2 certification

Description du poste

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data‑driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives. Labcorp is seeking a remote Senior Global Study Manager, Central Lab Services to join our team in Belgium. Work schedule: Monday - Friday

Job Responsibilities

Key contact for clients; Liaison between Clients, CRO, and Labcorp. Displays leadership to ensure successful interactions between Labcorp study team members needed to provide seamless study delivery to the client. Provides project management oversight; focusing on key client deliverables through budget, risk, and milestone management. Facilitates communications between Client and extended Labcorp study team, including Study Design Lead and Regional Study Coordinator. Performs review of SOW to ensure quality implementation of client specifics and requirements. Manages a portfolio of global, high‑complexity studies. Acts as an ambassador on behalf of the client within Labcorp CLS and across Labcorp business units; exemplifies the concept of Signature Client Service through outstanding, personalized customer service skills. Ensures that all customer expectations are documented and acted upon in compliance with regulatory requirements. Demonstrates through appropriate self‑organization the ability to manage conflicting priorities and to make difficult decisions. Able to act efficiently in an environment with dynamic timelines and priorities. Accountable for the implementation, monitoring and reporting of performance metrics. Actively participates in Labcorp CLS development through continuous process improvement, quality and productivity. Work with appropriate internal and external personnel to understand the culture and pipeline of assigned clients. Demonstrates strong interpersonal and communication skills that will build strong internal and external relationships to ensure deliverables are on time and within budget. Displays appropriate self‑organization and ability to manage conflicting priorities. Participate in functional meetings (eg. CLFs) and provide input, keeping processes up to date. Comply with LCLS Global Project Management strategy. Support a culture of continuous improvement, quality and productivity. Other duties as assigned.

Minimum Qualifications
  • Bachelor degree
  • 5 or more years of experience in pharmaceutical, biotechnology, CRO industry
  • 5 or more years of experience managing complex global clinical projects, including budget, risk, timeline and stakeholder management
  • 5 or more years experience in client facing (internal and external stakeholder) and stakeholder management.
  • 2 or more years of Central Labs experience
Preferred Qualifications
  • Master degree or University degree
  • Project Management training or certification (PMP, Prince2)
Additional Job Standards
  • Proven ability to drive project execution, influence cross‑functional teams and deliver results in a dynamic, fast‑paced environment
  • Ability to lead client communications confidently, manage expectations, influence outcomes, and build long‑term trusted partnerships.
  • Demonstrated leadership skills, including the ability to influence without direct authority, align cross‑functional teams, and remove roadblocks.
  • Proven ability to think beyond immediate project tasks and contribute to broader client, operational, and organizational objectives.
  • Customer‑focused and solution‑oriented approach, with a commitment to delivering an exceptional client experience
  • Demonstrated success in process improvement, change management or operational excellence initiatives
  • Excellent understanding of clinical trials, project management methodologies, and clinical development processes.
  • Strong ownership mindset with a demonstrated record of accountability, independent decision‑making, and successful execution of complex projects.
  • Proven ability to think strategically, anticipate challenges, and develop proactive solutions that support client and business objectives.

In this role you will support a key client account in leading pharma. The Senior Global Study Manager combines strong clinical project management expertise with strategic leadership and thrives in a client‑facing environment. Responsible for delivering complex global studies, you will drive key client deliverables, lead stakeholder communications, influence cross‑functional teams, manage risks and timelines, and foster collaboration across teams.

Get ready to redefine what’s possible and discover your extraordinary potential. Here at Labcorp, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning. Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.

Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility.

For more information about how we collect and store your personal data, please see our Privacy Statement. We believe in the power of science to change lives.

Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations to improve health and improve lives. Here, you can join our nearly 70,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care.

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