Clinical Trial Materials Technician

IQVIA; Livingston; Vor Ort; GBP 18.000 - 22.000; Vollzeit

Benefits dieser Stelle

Global exposure

Collaborative team

Cutting-edge technology

Career development

Work-life balance

Zusammenfassung

IQVIA Laboratories, site based in Livingston, is seeking a Clinical Trial Material Technician to support the assembly of test kits and materials in accordance with study protocols. You will prepare investigator instruction manuals and flowcharts, package completed kits with required documentation, and assemble shipping materials for investigators.

Careful inventory monitoring and proactive communication with your supervisor are necessary to avoid delays in study start-up.

Qualifikationen

• 0-6 months of relevant work experience preferred.
• Attention to detail and precision are essential.
• Proficient with standard computer applications.

Aufgaben

• Assemble test kits with specimen collection materials per protocol.
• Assemble investigator instruction manuals and flowcharts.
• Package completed test kits and required documentation for shipment.
• Prepare packages for shipping to investigators.
• Advise supervisor when supplies fall below required inventory levels.

Kenntnisse

Attention to detail

Basic computer skills

Excellent organizational skills

Jobbeschreibung

Clinical Trial Material Technician

IQIVIA Laboratories

Site based!

IQVIA Laboratories is a global leader in drug discovery and development, offering comprehensive central and specialty biomarker services. Our expertise includes genomics, immunoassays, flow cytometry, anatomic pathology, precision medicine, vaccine assays, ADME, and bioanalytical services. We also specialize in antibody and biomarker discovery and decentralized clinical trial solutions. Committed to scientific rigor and operational excellence, we support all phases of drug development, ensuring high data integrity and accelerating transformative therapies.

Join us on our exciting journey!

Job Overview:

Assemble test kits with specimen collection materials as per protocol.

Assemble investigator instruction manuals and flowcharts.

Package completed test kits, required documentation and required ancillary materials such as return shipping materials and bulk supplies for shipment to investigators.

Prepare packages for shipping.

Advise supervisor when supplies fall below required inventory levels in order to avoid delays in study start-up and resupply requirements .

Requirements:

• 0-6 months of relevant work experience preferred Pref
• Attention to detail.
• Basic computer skills.
• Excellent organizational skills.

Join IQVIA to see where your skills can take you

• Global exposure
• Collaborative and supportive team environment
• Access to cutting-edge and innovative, in-house technology
• Excellent career development and progression opportunities
• Work-Life Balance, with a strong focus on a positive well-being.

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.