Clinical Biospecimen Scientist - Single Sponsor Dedicated

IQVIA; Reading; On-site; GBP 55,000 - 75,000; Full time

Job summary

IQVIA in Reading, UK, seeks a Biospecimen Leader to shape strategy across global clinical trials. You will drive sample plans, oversee collection, analysis and data transfer, and guarantee data integrity from collection to study databases.

The role blends scientific expertise with cross-functional leadership, requiring strong organizational skills, SOP compliance and risk mitigation. You will set up labs, manage kit building and training for clinical sites, and oversee budgeted activities.

Qualifications

• Bachelor’s degree in Life Sciences or related field.
• Experience in clinical trials and biospecimen management.
• 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 with SOPs and risk mitigation.

Responsibilities

• Lead biospecimen strategy and define sample plans with clinical teams.
• Oversee biospecimen collection, analysis, and data transfer.
• Set up and manage labs for kit building, sample handling, and testing.
• Contribute to protocols and consent sections on samples.
• Identify and mitigate biospecimen risks.
• Develop lab manuals and training materials for sites.
• Ensure accurate data transfer and reconcile with data managers.
• Manage sample disposition at study end.
• Review proposals, forecast costs, validate invoices.

Skills

Biospecimen management

Clinical trials

Data integrity

SOP compliance

Lab operations

Cross-functional collaboration

Education

Bachelor’s degree in Life Sciences

Tools

LIMS knowledge

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.