Biomarker Operations Manager

Remote from: USA
Salary, yearly, USD: 98,000 - 105,000
Department: Healthcare & Medical
Employment type: Full Time,
Job posted: 5 Jun 2026
Apply before: 5 Jul 2026
Experience level: Midweight
Views / Applies: 66 / 13

Eurofins is a global group of laboratories providing laboratory services and products in the fields of food, environment, and pharmaceutical testing.

Medical Practice
1987

AI Summary

Eurofins Scientific seeks a Biomarker Operations Manager to join their dynamic team in a remote role supporting early-to late-stage clinical development. The manager will coordinate biomarker sample logistics, vendor operations, and cross-functional collaborations to ensure compliant sample collection, processing, and delivery. This role partners with Biomarker Program Leads and clinical study teams to align operational execution with strategic objectives. The position requires expertise in sample lifecycle management, vendor coordination, and issue resolution across multiple clinical trials. Ideal candidates have strong organizational skills and experience in clinical trial operations.

Role DNA

Job Complexity

Easy Hard

Pace & Pressure

Relaxed Fast-paced

Autonomy Level

Guided Full Ownership

Communication Load

Independent Highly Collaborative

AI Insight Balancing multiple clinical studies and coordinating complex sample logistics requires strong organizational skills and cross-functional communication, but does not involve strategic biomarker decision-making, placing it at a moderate difficulty.

Salary Analysis

AI Insight The offered salary range of $98,000 to $105,000 per year is competitive for a Biomarker Operations Manager role, falling near the median for similar positions in the US market. Based on industry data, the typical range for this role is $80,000 to $130,000, with the offered salary being slightly above the midpoint, reflecting the specialized nature of biomarker operations in clinical trials.

Key Skills

Biomarker Operations Clinical Trials Vendor Management Sample Logistics Cross-functional Collaboration Regulatory Compliance Project Management Data Management CRO Management Lifecycle Management

Cover Letter Sample

I am writing to express my strong interest in the Biomarker Operations Manager position at Eurofins Scientific. With extensive experience in clinical trial operations and biomarker sample logistics, I am confident in my ability to contribute to your dynamic team.

In my previous role, I successfully managed cross-functional teams to ensure timely sample collection, processing, and delivery for multiple studies. My expertise in vendor coordination and regulatory compliance aligns perfectly with the responsibilities of this position.

I am particularly drawn to Eurofins' leadership in life sciences and commitment to quality. I am eager to apply my skills to support your biomarker programs and advance clinical development.

Thank you for considering my application. I look forward to the possibility of discussing how I can add value to Eurofins.

Possible Interview Questions

Can you describe your experience with biomarker sample logistics in clinical trials?

I have managed sample collection, processing, and shipping for over 10 Phase I-III trials. This includes creating sample handling guidelines, tracking sample status, and coordinating with labs to ensure timely data delivery. I am proficient in using laboratory information management systems (LIMS) and have experience troubleshooting site issues.

How do you manage competing priorities across multiple studies?

I prioritize by assessing timelines and criticality of sample deliverables. I use project management tools to track progress and communicate proactively with stakeholders. For example, I once had overlapping sample shipments from two studies; I negotiated with the labs to adjust schedules and kept teams informed to avoid delays.

Describe a time you resolved a conflict between a vendor and a clinical site. How did you handle it?

A vendor reported improper sample labeling from a site. I contacted the site coordinator, provided retraining on protocols, and arranged a corrective shipment. I then updated the vendor on the resolution and implemented a checklist to prevent recurrence. This maintained compliance and preserved the site-vendor relationship.

What key factors do you consider when developing biomarker sample handling guidelines?

I consider sample stability, required processing steps (e.g., centrifugation, freezing), shipping conditions (dry ice, liquid nitrogen), and regulatory requirements (e.g., ICH-GCP, CLIA). I also consult with the scientific team to ensure the guidelines support the assay objectives. Clear instructions for site staff are crucial.

How do you stay current with regulations related to biomarker data privacy and informed consent?

I regularly review updates from regulatory bodies like FDA, EMA, and HIPAA guidelines. I also attend industry webinars and collaborate with legal teams. In my last role, I helped update consent forms to include explicit language about future research use and long-term storage duration, ensuring compliance.

Company Description

Eurofins 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 environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Job Description

We are seeking a highly motivated professional to join Eurofins’ Biomarker Operations group in a dynamic, cross-functional environment spanning early- to late-stage clinical development.

This is a full-time remote role. Candidates based in the Seattle, WA area may elect to attend onsite up to two days per week.

The Biomarker Operations Manager is responsible for the operational planning and logistics required to execute biomarker activities for clinical projects. This role does not own biomarker strategy or scientific decision-making; instead, it ensures that strategy is delivered effectively through rigorous sample lifecycle planning and oversight, vendor coordination, and cross-functional collaboration. In this position, you will serve as a clinical study team member responsible for coordinating biomarker sample logistics and vendor operations, ensuring compliant sample collection, processing, storage, and timely delivery to analytical laboratories. You will partner with Biomarker Program Leads to align operational execution with strategic objectives and collaborate closely with Clinical Operations, Study Start-Up, Clinical Data Management, laboratory vendors, and CROs to support workflow execution, risk mitigation, and issue resolution across clinical trials.

Responsibilities

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
Resolve biomarker sample-related questions from investigational sites, CROs, Clinical Operations, and Ethics Committees with appropriate cross-functional input
Review biomarker-specific informed consent language to ensure accurate description of sample collections, permissions for future research, and long term storage duration,
Review laboratory specifications and laboratory manuals to ensure protocol-defined biomarker samples, intended use, logistics, and storage are accurate and operationally feasible
Identify operational risks related to biomarker sample logistics, vendor performance, testing, and data delivery, and execute mitigation plans proactively
Partner with the Biomarker Program Lead to co-manage relationships with analytical biomarker laboratories supporting clinical trials
Oversee long-term storage, inventory tracking, and destruction of biomarker samples from clinical studies
Ensure accurate filing and maintenance of biomarker-related documents within the sponsor Trial Master File (TMF)
Lead and participate in continuous improvement initiatives focused on operational efficiency and process excellence

Qualifications

Minimum 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

Preferred Qualifications

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

Additional Information

This is a full-time position, Monday through Friday, 8:00 a.m. to 5:00 p.m., with flexibility to accommodate select early-morning meetings that support East Coast schedules
Weekend, overtime, and holiday work may be required based on business needs
West Coast candidates are preferred. The position may be fully remote or hybrid for Seattle-area candidates
Comprehensive full-time benefits, including medical, dental, and vision coverage
Life and disability insurance
401(k) with company match
Paid vacation and company holidays
Pay range $98,000-$105,000 per year.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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