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- Tasks: Manage clinical trial samples and support study teams for optimal execution.
- Company: Join Parexel, a leader in clinical studies with a commitment to improving global health.
- Benefits: Enjoy a fully remote role with competitive pay and opportunities for professional growth.
- Why this job: Make a real impact on patient well-being through innovative clinical trials.
- Qualifications: 6+ years in the industry with a science background and knowledge of medical terms.
- Other info: Be part of a passionate team dedicated to advancing healthcare solutions.
The predicted salary is between 36000 - 60000 £ per year.
In this position you will be an invaluable resource working closely with line manager, and other key personnel to implement and operationalize the department’s goals within client clinical trials. Manages central laboratory and specialty vendors across a mix of varyingly complex clinical trials. Performs other duties as necessary to ensure optimal clinical trial execution.
Responsibilities:
- 100% homebased position
- Manages acquisition of clinical trial samples
- Provides support for sample related matters to clinical study teams
- Works with ICF Specialist and wider team to ensure compliance with ICF permissions
- Assists with vendor selection and oversight
- Provides input to clinical trial related documents under the supervision of the Lead
- Executes biomarker plans in collaboration with the study team and Lead
- Prepares request for proposals, reviews and assesses bids and Statement of Work (SOW)
- Works closely with line manager, and other key personnel to implement and operationalize the department’s goals within client clinical trials
Qualifications:
- Minimum of 6 years relevant industry experience is required.
- Science background and working knowledge of a wide array of medical terms, biological assays including proteomics, cellular assays and genomics.
- Understanding of bioethics of human biospecimen collection and research.
- Oncology experience preferred.
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients. You’ll be an influential member of the wider team.
What we are looking for in this role: For every role, we look for professionals who have the determination and courage always to put patient well-being first. 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.
Parexel FSP are currently recruiting for a Senior Clinical Vendor Specialist in the UK. This is a 100% remote position and is dedicated to one of our key global sponsors.
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Senior Clinical Vendor Specialist - BioSamples/Central Laboratory - Remote - FSP employer: Parexel
Contact Detail:
Parexel Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Vendor Specialist - BioSamples/Central Laboratory - Remote - FSP
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at Parexel or similar companies. A friendly chat can lead to insider info about job openings and even referrals that could give you an edge.
✨Tip Number 2
Prepare for virtual interviews by practising common questions related to clinical trials and vendor management. Make sure you can articulate your experience with biomarker plans and compliance issues clearly and confidently.
✨Tip Number 3
Showcase your passion for patient well-being during interviews. Share specific examples of how you've put patients first in your previous roles, as this aligns perfectly with Parexel's mission.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, joining our Talent Community means you’ll be the first to know about new opportunities that match your skills.
We think you need these skills to ace Senior Clinical Vendor Specialist - BioSamples/Central Laboratory - Remote - FSP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Clinical Vendor Specialist role. Highlight your relevant experience in managing clinical trials and vendor oversight, as well as any specific skills related to bioethics and biological assays.
Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this position. Share your passion for improving patient well-being and how your background aligns with our goals at Parexel.
Showcase Your Experience: In your application, be sure to showcase your 6+ years of industry experience. Mention specific projects or trials you've worked on that demonstrate your expertise in oncology and clinical sample management.
Apply Through Our Website: We encourage you to apply directly through our website. This way, we can easily track your application and ensure it gets the attention it deserves. Plus, you'll be part of our talent community for future opportunities!
How to prepare for a job interview at Parexel
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trials, especially in relation to bioethics and the specific medical terms mentioned in the job description. Being able to discuss your experience with biological assays and oncology will show that you're not just familiar with the field, but that you’re genuinely passionate about it.
✨Showcase Your Team Spirit
Since this role involves working closely with various teams, be prepared to share examples of how you've successfully collaborated in the past. Highlight your ability to manage vendor relationships and support clinical study teams, as this will demonstrate your fit for the collaborative nature of the position.
✨Prepare Questions
Interviews are a two-way street! Prepare insightful questions about the company’s approach to clinical trials and how they ensure compliance with ICF permissions. This shows that you’re not only interested in the role but also in how you can contribute to their goals.
✨Be Ready to Discuss Challenges
Think of specific challenges you've faced in previous roles, particularly those related to managing complex clinical trials or vendor oversight. Be ready to explain how you overcame these challenges, as this will highlight your problem-solving skills and resilience, which are crucial for this position.