Clinical Trials Sourcing Specialist - Global
Clinical Trials Sourcing Specialist - Global

Clinical Trials Sourcing Specialist - Global

London Full-Time 36000 - 60000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Join our team to develop sourcing strategies for clinical trial materials and services.
  • Company: Cencora is a global leader in clinical supply services, dedicated to improving health outcomes.
  • Benefits: Enjoy flexible work options, competitive pay, and opportunities for professional growth.
  • Why this job: Make a real impact on health while collaborating with diverse teams in an innovative environment.
  • Qualifications: Bachelor's or master's degree required; 5+ years in strategic sourcing preferred.
  • Other info: This role offers hybrid or fully remote options across various EMEA locations.

The predicted salary is between 36000 - 60000 £ per year.

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!

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 a Sourcing 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 (note that level will be decided after interview depending on skills/competencies).

Responsibilities:

  • Collaborate with the Sourcing Manager to develop sourcing strategies for clinical trials materials, services, and suppliers based on project requirements and organizational goals.
  • Conduct market research to identify potential suppliers/vendors that meet quality standards, cost-effectiveness requirements, timelines, and regulatory compliance.
  • Analyse trends and forecasting of required products to anticipate market shortages and potential sourcing opportunities.
  • 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.
  • Ensure compliance with relevant regulations/guidelines such as Good Clinical Practice (GCP) throughout all stages of clinical trial material/services procurement.
  • Responsible for maintaining contemporaneous data of product availability and critical information.
  • Collaborate with Proposal development team on tenders with strategic sourcing, cultivating relationships with prospective manufacturers and wholesalers providing a value solution for the clients.
  • 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.
  • Liaise with internal stakeholders (e.g., Clinical Operations) to understand project needs, timelines, specifications, budget constraints; align sourcing strategies accordingly.
  • Communicate effectively with Operations to ensure a smooth transition from quote/Purchase Order (PO) to delivery, e.g. timelines.
  • Identify opportunities for process improvements within the clinical trials sourcing function; propose changes aimed at optimizing efficiency/effectiveness through automation/digitization where applicable.
  • 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.
  • Provide necessary information and support, documentation, and support to assist in determining root causes, implementing corrective actions, and preventing future occurrences.

Qualifications & Experience:

  • Bachelor's or master's degree in business administration, supply chain management, life sciences, or a related field.
  • 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:

  • Solid knowledge of strategic sourcing methodologies and best practices.
  • Knowledge of APAC & LATAM comparator market.
  • Supports forecasting (tailor advice) and strategy work.
  • Familiarity with clinical trial materials/services and their specific sourcing requirements.
  • Proficiency in supplier evaluation, negotiation, and contract management.
  • Strong analytical and problem-solving abilities.
  • Effective communication and interpersonal skills.
  • Strong understanding of clinical trials sourcing processes and regulations.
  • Strong client building and 3rd party relationship management.
  • Outstanding ability to provide customer service with the highest standards of quality and excellence.
  • 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.

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.

Clinical Trials Sourcing Specialist - Global employer: AmerisourceBergen

At Cencora, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises collaboration and innovation in the healthcare sector. Our team members enjoy flexible working arrangements across various EMEA locations, alongside comprehensive benefits and opportunities for professional growth, all while contributing to meaningful projects that improve lives globally.
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Contact Detail:

AmerisourceBergen Recruiting Team

hrsc@cencora.com

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Trials Sourcing Specialist - Global

✨Tip Number 1

Familiarise yourself with the latest trends in clinical trial sourcing and procurement. Understanding the current market landscape will help you engage in meaningful conversations during interviews and demonstrate your expertise.

✨Tip Number 2

Network with professionals in the pharmaceutical and healthcare industries. Attend relevant conferences or webinars to connect with potential colleagues and learn about the latest developments in clinical trials, which can give you an edge in discussions.

✨Tip Number 3

Prepare to discuss specific examples of how you've successfully managed sourcing strategies or supplier relationships in the past. Highlighting your experience with risk management and compliance will show that you're ready for the challenges of this role.

✨Tip Number 4

Research Cencora and its mission to create healthier futures. Being able to articulate how your values align with the company's purpose will make a strong impression and demonstrate your genuine interest in joining their team.

We think you need these skills to ace Clinical Trials Sourcing Specialist - Global

Strategic Sourcing Methodologies
Market Research and Analysis
Risk Management and Mitigation Strategies
Regulatory Compliance (GCP)
Supplier Evaluation and Negotiation
Contract Management
Analytical Skills
Problem-Solving Abilities
Effective Communication Skills
Interpersonal Skills
Understanding of Clinical Trials Sourcing Processes
Client Relationship Management
Process Improvement Initiatives
Cross-Functional Collaboration
Fluency in English

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in strategic sourcing and procurement, particularly within the pharmaceutical or healthcare industry. Use keywords from the job description to demonstrate your fit for the role.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for improving health outcomes and your understanding of clinical trials. Mention specific experiences that align with the responsibilities outlined in the job description.

Highlight Relevant Skills: Emphasise your analytical abilities, communication skills, and knowledge of regulatory compliance in your application. Provide examples of how you've successfully managed sourcing strategies or collaborated with cross-functional teams.

Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the clinical trials environment.

How to prepare for a job interview at AmerisourceBergen

✨Understand the Role

Make sure you thoroughly understand the responsibilities of a Clinical Trials Sourcing Specialist. Familiarise yourself with sourcing strategies, market research, and compliance regulations like Good Clinical Practice (GCP). This will help you answer questions confidently and demonstrate your knowledge.

✨Showcase Your Experience

Highlight your relevant experience in strategic sourcing or procurement, especially within the pharmaceutical or healthcare industry. Be prepared to discuss specific examples of how you've successfully managed sourcing activities or mitigated risks in previous roles.

✨Prepare for Scenario Questions

Expect scenario-based questions that assess your problem-solving abilities and risk management skills. Think of examples where you've had to analyse trends, forecast needs, or handle supply chain disruptions, and be ready to explain your thought process.

✨Demonstrate Collaboration Skills

Since the role involves cross-functional collaboration, be prepared to discuss how you've worked with different teams in the past. Highlight your communication skills and ability to build relationships with stakeholders, as this is crucial for ensuring seamless integration of clinical trial supplies.

Clinical Trials Sourcing Specialist - Global
AmerisourceBergen
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