Eurofins

Eurofins

Biomarker Operations Manager

UKRemotePosted 8 days ago$98,000 – $105,000
Full TimeSeniorRemoteUK

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Job Description

Company DescriptionEurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our en

Key Highlights

  • Partner with colleagues across the Biomarkers Department to support biomarker implementation in clinical studies and advance program goals through a translational understanding of disease states and treatment modalities
  • Serve as a key member of clinical study teams across multiple disease-area programs, providing operational guidance on biomarker sample logistics and vendor management
  • Develop and maintain biomarker sample handling guidelines for collection, processing, shipping, and long-term storage
  • Track clinical biomarker sample location and testing status through study completion, ensuring data delivery aligns with study-specific timelines
  • Manage cross-trial biomarker sample testing logistics and develop timelines with laboratories, strategically coordinating shipment and testing schedules across multiple studies and proactively mitigate competing priorities

Qualifications

Required Qualifications

  • At least 2 years of direct experience with clinical data management
  • Working knowledge of Good Clinical Practice (GCP), clinical trial execution, and the roles and interactions of key stakeholders involved in clinical trial delivery; significant sponsor-side experience supporting clinical trials is required
  • Demonstrated ability to collaborate effectively with scientists, clinical teams, laboratory vendors, and cross-functional stakeholders
  • Ability to independently manage biomarker sample logistics and operational activities across multiple studies and programs
  • Strong computer skills are required, including demonstrated ability to manage complex sample metadata across multiple Excel files, timelines, PowerPoint summaries, and operational tracking tools
  • Excellent written and verbal communication skills, with strong organizational skills, attention to detail, and the ability to prioritize effectively in a fast-paced environment
  • Authorization to work in the United States indefinitely without restriction or sponsorship
  • At least 2 years of direct experience with clinical data management
  • Working knowledge of Good Clinical Practice (GCP), clinical trial execution, and the roles and interactions of key stakeholders involved in clinical trial delivery; significant sponsor-side experience supporting clinical trials is required
  • Demonstrated ability to collaborate effectively with scientists, clinical teams, laboratory vendors, and cross-functional stakeholders
  • Ability to independently manage biomarker sample logistics and operational activities across multiple studies and programs
  • Strong computer skills are required, including demonstrated ability to manage complex sample metadata across multiple Excel files, timelines, PowerPoint summaries, and operational tracking tools
  • Excellent written and verbal communication skills, with strong organizational skills, attention to detail, and the ability to prioritize effectively in a fast-paced environment
  • Authorization to work in the United States indefinitely without restriction or sponsorship
  • General Understanding of biomarker research, development, and clinical implementation
  • Advanced proficiency with project management platforms or sample tracking systems (for example, Smartsheet or LIMS)
  • Experience with scripting in R

Skills & Technologies

GCP

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Job Details

Employment Type

Full Time

Experience Level

Senior

Salary Range

$98,000 – $105,000

Location

UK

Work Mode

Remote

Posted

8 days ago

Country

UK