Be at the heart of actionFly remote-controlled drones into enemy territory to gather vital information.

Apply Now

Sourcing Global Clinical Trials- Project Manager

Cencora | Pharma solutions
London
2 months ago
Create job alert

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!

Job Details

Alcura, a Cencora company, offers end-to-end clinical supply services and world-class healthcare partnership supported by local expertise with global reach. The world’s foremost pharmaceutical companies, healthcare providers, and their patients count on us to deliver comprehensive and personalized clinical trial solutions.

We have a vacancy for Project Manager/Sr Project Manager to join our Global Clinical Supplies Team in the EMEA region. This can be office based, hybrid, or fully homebased in a number of EMEA locations- Spain, UK, Germany (note that level will be decided after interview depending on skills/competencies).

Responsibilities:

Sourcing Strategy Development

  1. Collaborate with the Sourcing Manager to develop sourcing strategies for clinical trials materials, services, and suppliers based on project requirements and organizational goals.
  2. Conduct market research to identify potential suppliers/vendors that meet quality standards, cost-effectiveness requirements, timelines, and regulatory compliance.
  3. Analyse trends and forecasting of required products to anticipate market shortages and potential sourcing opportunities.

Risk Management & Compliance

  1. Identify potential risks associated with sourcing activities (e.g., supply chain disruptions), develop risk mitigation strategies/crisis management plans to minimize impact on clinical trial operations.
  2. Ensure compliance with relevant regulations/guidelines such as Good Clinical Practice (GCP) throughout all stages of clinical trial material/services procurement.
  3. Responsible for maintaining contemporaneous data of product availability and critical information.

Cross-functional Collaboration

  1. Collaborate with Proposal development team on tenders with strategic sourcing, cultivating relationships with prospective manufacturers and wholesalers providing a value solution for the clients.
  2. Collaborate closely with cross-functional teams including Operations personnel (clinical operations teams), quality assurance/quality control (QA) teams, Qualified presumption of safety (QPs), Supply chain, to ensure seamless integration of clinical trial supplies/services into ongoing operations.
  3. Liaise with internal stakeholders (e.g., Clinical Operations) to understand project needs, timelines, specifications, budget constraints; align sourcing strategies accordingly.
  4. Communicate effectively with Operations to ensure a smooth transition from quote/Purchase Order (PO) to delivery, e.g. timelines.

Continuous Improvement Initiatives

  1. Identify opportunities for process improvements within the clinical trials sourcing function; propose changes aimed at optimizing efficiency/effectiveness through automation/digitization where applicable.

Quality Management System

  1. Support Lead Project Manager Comparator Operations/Quality Assistant team to investigate any customer complaints or deviations or audits related to sourced pharmaceutical drugs for clinical trials.
  2. Provide necessary information and support, documentation, and support to assist in determining root causes, implementing corrective actions, and preventing future occurrences.

Qualifications & Experience:

  1. Bachelor's or master's degree in business administration, supply chain management, life sciences, or a related field.
  2. 5 + years of experience in strategic sourcing or procurement roles, preferably within the pharmaceutical or healthcare industry- clinical supplies in a clinical trial environment.

Skills Required:

  1. Solid knowledge of strategic sourcing methodologies and best practices.
  2. Knowledge of APAC & LATAM comparator market.
  3. Supports forecasting (tailor advise) and strategy work.
  4. Familiarity with clinical trial materials/services and their specific sourcing requirements.
  5. Proficiency in supplier evaluation, negotiation, and contract management.
  6. Strong analytical and problem-solving abilities.
  7. Effective communication and interpersonal skills.
  8. Strong understanding of clinical trials sourcing processes and regulations.
  9. Strong client building and 3rd party relationship management.
  10. Outstanding ability to provide customer service with the highest standards of quality and excellence.
  11. Fluent in English- the hiring process will be conducted in this language.

What Cencora offers

Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.

Affiliated Companies

Affiliated Companies: Alcura Health España S.A.

Equal Employment Opportunity

Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.

The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.

Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email . We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned.


#J-18808-Ljbffr

Related Jobs

View all jobs

Clinical Trials Sourcing Specialist - Global

Sr. Manager, Regulatory Affairs Labeling Execution

Occupational Health Advisor

Regulatory Affairs Manager

EU Deforestation Administrator

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Why Medical Technology Careers in the UK Are Becoming More Multidisciplinary

Medical technology (medtech) is transforming healthcare in the UK — from wearable sensors to AI diagnostic tools, from surgical robots to telemedicine platforms. Advances in hardware, software, data and connectivity are enabling more personalized, efficient and accessible care. But with great power comes great responsibility. As medical devices and health technologies enter hospitals, clinics and consumers’ homes, professionals in this domain must master much more than engineering and algorithms. They must also understand law, ethics, psychology, linguistics & design. That is, medtech careers are now deeply multidisciplinary. In this article, we explore why medical technology careers in the UK are becoming more multidisciplinary, how these five allied fields now intersect with medtech work, and what job-seekers and employers should do to succeed in this evolving ecosystem.

Medical Technology Team Structures Explained: Who Does What in a Modern MedTech Department

Medical technology (MedTech) spans everything from wearable health devices and surgical robots to diagnostic imaging, in-vitro diagnostics (IVD), digital therapeutics, AI-driven triage, and Class I–III medical devices. In the UK, the sector touches NHS care pathways, private providers, and global markets—with stringent expectations for safety, clinical evidence, cybersecurity, and data privacy. As ventures scale from prototype to regulated product, clear team structures become the difference between promising pilots and licensed, market-ready devices. Whether you’re hiring your first clinical specialist or applying for a role in QA/RA, this guide explains who does what in a modern MedTech department, how functions collaborate across the product lifecycle, UK-typical skill sets and salaries, common pitfalls, and best practices for building a resilient team.

Why the UK Could Be the World’s Next Medical Technology Jobs Hub

Medical technology—often abbreviated as medtech—is one of the fastest-growing sectors in healthcare. From sophisticated diagnostic devices and surgical robotics to wearable health monitors and AI-powered imaging systems, innovation in medical technology is transforming patient care, streamlining hospital processes, and enabling personalised treatment at scale. As the United Kingdom deepens its commitment to healthcare innovation, demand for professionals skilled in medtech development, regulation, manufacturing, and deployment is surging. With a rich heritage of scientific research, a globally respected healthcare system, and a dynamic life-sciences ecosystem, the UK is ideally placed to become the world’s next medical technology jobs hub. This article explores why the UK has this potential, where demand is strongest, what kinds of roles are emerging, and what must happen to ensure the UK fulfils its role as a global centre for medtech careers.