Clinical Biospecimen Scientist

Iqvia

Reading

On-site

GBP 65,000 - 90,000

Full time

8 days ago

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Job summary

IQVIA is seeking a biospecimen leader in Reading, UK, to drive strategy and manage all biospecimens across global clinical trials. You will oversee collection, analysis, data transfer, and sample disposition, ensuring data integrity and protocol alignment.

The role requires a strong background in clinical trials, lab operations, and risk mitigation, with the ability to collaborate across functions and geographies. A Life Sciences degree and hands-on SOP expertise are essential.

Qualifications

  • Bachelor’s degree in Life Sciences or related field.
  • Strong background in clinical trials and biospecimen management.
  • Deep knowledge of sample logistics and ethical considerations.
  • Ability to collaborate across functions and geographies.
  • Strong organizational and problem-solving skills.
  • Technical expertise in lab operations and data integrity.
  • Proficiency in SOP compliance and risk mitigation.

Responsibilities

  • Lead Biospecimen Strategy: Collaborate with clinical development teams to define and execute sample plans.
  • Own the Lifecycle: Oversee collection, analysis, and data transfer for all biospecimens.
  • Technical Leadership: Set up and manage labs for kit building, sample handling, and testing.
  • Protocol Expertise: Provide input on sample-related sections in protocols and consents.
  • Risk Management: Identify and escalation biospecimen-related risks; implement solutions.
  • Training & Support: Develop lab manuals and training materials for clinical sites.
  • Data Excellence: Ensure accurate data transfer and reconciliation with trial data managers.
  • Close-Out Mastery: Manage sample disposition—storage, return, or disposal—at study end.
  • Budget Oversight: Review lab proposals, forecast costs, and validate invoices.

Skills

Biospecimen management
Clinical trial coordination
Data integrity
SOP compliance

Education

Bachelor’s degree in Life Sciences

Tools

Lab equipment handling
Data management systems

Job description

Your Mission

Be the biospecimen champion in global clinical trials! Drive strategy, ensure flawless sample collection and analysis, and guarantee data integrity. Your expertise powers breakthrough science and accelerates life-changing therapies.

What You’ll Do
  • Lead Biospecimen Strategy: Collaborate with clinical development teams to define and execute sample plans.
  • Own the Lifecycle: Oversee collection, analysis, and data transfer for all biospecimens.
  • Technical Leadership: Set up and manage labs for kit building, sample handling, and testing.
  • Protocol Expertise: Provide input on sample-related sections in protocols and consents.
  • Risk Management: Identify and escalation biospecimen-related risks; implement solutions.
  • Training & Support: Develop lab manuals and training materials for clinical sites.
  • Data Excellence: Ensure accurate data transfer and reconciliation with trial data managers.
  • Close-Out Mastery: Manage sample disposition—storage, return, or disposal—at study end.
  • Budget Oversight: Review lab proposals, forecast costs, and validate invoices.
What You Bring
  • Education: Bachelor’s degree in Life Sciences or related field.
  • Experience: Strong background in clinical trials and biospecimen management.
  • Skills That Shine:
    • Deep knowledge of sample logistics and ethical considerations.
    • Ability to collaborate across functions and geographies.
    • Strong organizational and problem-solving skills.
    • Technical expertise in lab operations and data integrity.
    • Proficiency in SOP compliance and risk mitigation.
Core Strengths
  • Collaboration
  • Innovation
  • Ownership
  • Quality Focus
  • Communication

Please note this role is not eligible for the UK visa sponsorship.

Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

About Us

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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