At a Glance
- Tasks: Lead procurement strategies for clinical trial management and collaborate with cross-functional teams.
- Company: Join Teva, a leading biopharmaceutical company dedicated to innovation and patient care.
- Benefits: Enjoy comprehensive health insurance, retirement savings, and generous paid time off.
- Other info: Hybrid work model with opportunities for professional development and career advancement.
- Why this job: Make a real impact in healthcare while growing your career in a dynamic environment.
- Qualifications: 7+ years in procurement or related fields, with experience in clinical development preferred.
The predicted salary is between 56250 - 68750 £ per year.
We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.
The Associate Director – Clinical Trial Management Business Partnering & Category Strategy is an experienced procurement professional responsible for category management and sourcing activities supporting clinical trial management across Phases 1–4. The role partners with Clinical Development and other stakeholders to translate study needs, outsourcing requirements, market intelligence, and supplier capabilities into practical sourcing and supplier strategies that support cost, quality, speed, flexibility, and business objectives.
This role is hybrid 2-3 days in our West Chester, PA site.
How You’ll Spend Your Day
- Partner with Clinical Development and Clinical Operations stakeholders to understand study requirements, portfolio priorities, outsourcing needs, and business objectives within Clinical Trial Management.
- Develop and maintain category strategies and sourcing roadmaps for assigned Clinical Trial Management services, including FSO, FSP, and related clinical operations support.
- Provide category and supplier insights to support business decisions, supplier selection, and outsourcing model considerations.
- Use spend data, supplier insights, benchmarks, and market intelligence to identify sourcing, productivity, and value opportunities within assigned categories.
- Develop category-level value initiatives that may include rate optimization, demand management, supplier consolidation, resourcing-model improvements, and commercial standardization.
- Track sourcing outcomes, value delivery, and key category activities using established Procurement tools and reporting mechanisms.
- Support supplier segmentation, governance, performance management, and improvement activities for key CRO, FSP, and clinical operations suppliers within assigned categories.
- Maintain current knowledge of CRO capabilities, FSP/FSO operating models, capacity trends, pricing dynamics, and relevant clinical outsourcing market developments.
- Lead or support sourcing initiatives for Clinical Trial Management services, including requirements development, RFx activities, supplier evaluation, negotiation, recommendation, and contracting support.
- Apply established category management, sourcing, supplier governance, and value-tracking practices consistently across assigned work.
Your Skills and Experience
- 7+ years of progressive experience in procurement, category management, strategic sourcing, supplier management, clinical operations, or related disciplines.
- Experience supporting sourcing, category management, supplier governance, or commercial activities for clinical development services, preferably including CROs and FSP/FSO models.
- Working understanding of pharmaceutical drug development, clinical trial execution, clinical outsourcing models, supplier ecosystems, and relevant regulatory requirements.
- Demonstrated ability to manage cross-functional sourcing projects, analyze commercial information, influence stakeholders, and deliver measurable outcomes.
EDUCATION & EXPERIENCE
- Bachelor’s degree required; advanced degree preferred in Business, Supply Chain, Life Sciences, Finance, or related field.
- Master’s degree with 5+ years of relevant experience, or Bachelor’s degree with 7+ years of relevant experience.
Salary Range
We offer a competitive benefits package, including comprehensive health insurance, retirement savings, paid time off, and life and disability protection.
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.
Associate Director R&D Procurement - Clinical Trial Management in Chester employer: Tevapharm
At Teva, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work culture that fosters collaboration and innovation. As a Neuroscience Sales Specialist in Birmingham, AL, you will benefit from comprehensive health insurance, generous paid time off, and robust employee growth opportunities, all while making a meaningful impact on global health. Join us to thrive in a supportive environment that values your contributions and encourages professional development.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director R&D Procurement - Clinical Trial Management in Chester
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We think you need these skills to ace Associate Director R&D Procurement - Clinical Trial Management in Chester
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Tevapharm!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Tevapharm that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Tevapharm!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Tevapharm, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Tevapharm
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Tevapharm that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
