Laboratory Assistant

Posted 17 Days Ago
Be an Early Applicant
Budapest, HUN
In-Office
Entry level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Supports the preparation, processing, labeling, storage, tracking, documentation, and shipment of biological samples for Phase I clinical research studies. Prepares laboratory materials, maintains equipment and inventory, follows GCP, GLP, SOP, safety, and quality requirements, and collaborates with clinical and laboratory teams to ensure accurate, compliant sample handling.
Summary Generated by Built In
Clinical Laboratory Assistant

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


At ICON's state-of-the-art Phase I Clinical Research Unit (CRU) in Budapest, you will play a critical role in supporting the processing, handling, storage, and shipment of clinical trial samples generated during early phase studies. Working closely with clinical and laboratory teams, you will help ensure the accurate processing of pharmacokinetic (PK), biomarker, and other biological samples while maintaining the highest standards of quality, compliance, and patient safety. This role is focused on sample processing activities rather than diagnostic testing and provides an excellent opportunity for individuals with a laboratory technician or laboratory assistant background to contribute to the development of new medicines.
What You Will Be Doing
  • Support the preparation, processing, labelling, storage, and tracking of biological samples in accordance with study protocols and laboratory procedures.
  • Prepare laboratory reagents, consumables, and equipment required to support clinical and analytical testing activities.
  • Maintain laboratory facilities, equipment, and inventory to ensure operational readiness and compliance with quality standards.
  • Complete and maintain accurate laboratory documentation, records, and sample tracking information in line with GCP, GLP, and regulatory requirements.
  • Work collaboratively with laboratory and clinical teams to support the efficient delivery of Phase I clinical research studies.
  • Promote a safe and compliant working environment by adhering to SOPs, health and safety regulations, and quality processes.
You Will Have/Be
  • High school diploma or equivalent required; a qualification in a scientific, laboratory, or healthcare-related discipline is preferred.
  • Previous experience working in a laboratory, healthcare, clinical research, or other regulated environment would be advantageous.
  • Strong attention to detail with the ability to accurately handle samples, documentation, and laboratory records.
  • Excellent organisational skills with the ability to manage multiple tasks in a fast-paced environment.
  • Effective communication and teamwork skills, with a proactive and flexible approach to supporting operational activities.
  • Commitment to quality, compliance, and patient safety, with a willingness to learn and develop within clinical research.

#LI-RD1


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Skills Required

  • High school diploma or equivalent
  • Qualification in a scientific, laboratory, or healthcare-related discipline
  • Previous experience in a laboratory, healthcare, clinical research, or regulated environment
  • Strong attention to detail when handling samples, documentation, and laboratory records
  • Excellent organizational skills and ability to manage multiple tasks
  • Effective communication and teamwork skills
  • Commitment to quality, compliance, and patient safety

ICON plc Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ICON plc and has not been reviewed or approved by ICON plc.

  • Healthcare Strength Benefits are described as comprehensive, with medical coverage and wellness initiatives highlighted. Larger sites are also associated with added wellness supports such as onsite fitness options and access to an employee assistance program.
  • Leave & Time Off Breadth Time-off and flexibility provisions are positioned as a meaningful part of the total package, including vacation/annual leave and flexible work scheduling. Flexibility is sometimes cited as helping offset long hours in certain roles.
  • Retirement Support Retirement and savings support is presented as a core component of the benefits package, including offerings such as pension arrangements in some locations and a U.S. 401(k) plan with company match. Financial planning resources are also emphasized as part of broader security benefits.

ICON plc Insights

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The Company
HQ: Dublin
34,685 Employees
Year Founded: 1990

What We Do

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

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